Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Water. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Water SCHEMBL226693 | 1.00 | — | — | |
| Water SCHEMBL1133296 | 1.00 | — | — | |
| Bromide SCHEMBL1159481 | 0.82 | — | — | |
| Bromide SCHEMBL66683 | 0.82 | — | — | |
| Bromide SCHEMBL5945150 | 0.82 | — | — | |
| Water SCHEMBL25327325 | 0.67 | — | — | |
| Water SCHEMBL5712989 | 0.67 | — | — | |
| Bromide SCHEMBL4564556 | 0.67 | — | — | |
| Water SCHEMBL3699635 | 0.67 | — | — | |
| Water SCHEMBL11727068 | 0.67 | — | — |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 241 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120082281-A | Preparation method of two-dimensional porous double transition metal oxide composite self-repairing noise-reducing anticorrosive coating | 中国海洋大学 | 2025-06-03 | — | — | CN | claimed |
| CN-118807760-A | Heterojunction catalyst, preparation method and application | 中国科学技术大学 | 2024-10-22 | — | — | CN | claimed |
| CN-118715213-A | Process for preparing N- (1-methylcyclopropyl) -2- (3-pyridinyl) -2H-indazole-4-carboxamide and intermediates thereof | FMC公司 | 2024-09-27 | — | — | CN | claimed |
| CN-118047735-A | Preparation method of pramoxine | 中国人民解放军空军军医大学 | 2024-05-17 | — | — | CN | claimed |
| CN-117586106-A | Method for synthesizing alkylaryl ether | 中国人民解放军空军军医大学 | 2024-02-23 | — | — | CN | claimed |
| CN-114751993-B | Preparation method of cellulose nanocrystalline capable of being dried and redispersed | 陕西科技大学 | 2023-09-01 | — | — | CN | claimed |
| WO-2023158769-A1 | PROCESSES FOR THE PREPARATION OF N-(1- METHYLCYCLOPROPYL)-2-(3 -PYRIDINYL)-2H- INDAZOLE-4-CARBOXAMIDE AND INTERMEDIATES THEREOF | FMC CORPORATION (US) | 2023-08-24 | — | — | WO | claimed |
| CN-114478371-B | Application of nickel/ketone double-catalysis system in cross-coupling reaction of halogenated aromatic hydrocarbon and aryl sodium sulfinate | 苏州大学 | 2023-07-04 | — | — | CN | claimed |
| CN-109694350-B | Compound containing fluoromethyl and preparation method thereof | 中国科学院上海有机化学研究所 | 2023-05-09 | — | — | CN | claimed |
| CN-114751993-A | Preparation method of cellulose nanocrystal capable of being dried and redispersed | 陕西科技大学 | 2022-07-15 | — | — | CN | claimed |
| CN-114716466-A | Method for preparing chiral alpha-amino boric acid/boric acid ester through nickel-catalyzed asymmetric hydroamidation | 南京大学 | 2022-07-08 | — | — | CN | claimed |
| CN-105669365-B | Aryl or heteroaryl compound containing difluoroalkyl substitution, preparation method and application | 中国科学院上海有机化学研究所 | 2022-06-21 | — | — | CN | claimed |
| CN-112939750-B | Method for transferring asymmetric functionalization by nickel-hydrogen catalysis olefin promoted by ligand relay strategy | 南京大学 | 2022-05-17 | — | — | CN | claimed |
| CN-113754689-A | Nickel-catalyzed asymmetric hydroamination method for olefin | 南京大学 | 2021-12-07 | — | — | CN | claimed |
| CN-112939750-A | Method for transferring asymmetric functionalization by nickel-hydrogen catalysis olefin promoted by ligand relay strategy | 南京大学 | 2021-06-11 | — | — | CN | claimed |
| CN-112679290-A | Nickel-catalyzed asymmetric hydrogen alkynylation method for olefins and application of nickel-catalyzed asymmetric hydrogen alkynylation method in preparation of AMG837 | 南京大学 | 2021-04-20 | — | — | CN | claimed |
| CN-112047925-A | Preparation method of N- (aryl/heteroaryl) alkyl-diamide | 中国科学院兰州化学物理研究所 | 2020-12-08 | — | — | CN | claimed |
| CN-110878012-A | Synthetic method of E-type methyl styrene compound | 南京大学 | 2020-03-13 | — | — | CN | claimed |
| US-20170271637-A1 | METHOD OF MANUFACTURING POROUS POLYMER MEMBRANE USING WATER PRESSURE AND BATTERY SEPARATOR COMPRISING POROUS POLYMER MEMBRANE MANUFACTURED BY THE METHOD | SANGMYUNG UNIVERSITY SEOUL INDUSTRY ACADEMY COOPERATION FOUNDATION (KR) | 2017-09-21 | — | — | US | claimed |
| EP-4678652-A1 | METHOD FOR PRODUCING CYCLIC PEPTIDE COMPOUND | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2026-01-14 | — | — | EP | disclosed |
| US-20260001889-A1 | COMPOSITIONS USEFUL FOR MODULATING SPLICING | SKYHAWK THERAPEUTICS INC (US) | 2026-01-01 | — | — | US | disclosed |
| US-12410212-B2 | Cyclic compound having selective KRAS inhibitory effect on HRAS and NRAS | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2025-09-09 | — | — | US | disclosed |
| EP-4603105-A1 | PHARMACEUTICAL COMPOSITION CONTAINING CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT AGAINST HRAS AND NRAS | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2025-08-20 | — | — | EP | disclosed |
| US-20250256222-A1 | METHOD OF TREATING AN OIL SPILL | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2025-08-14 | — | — | US | disclosed |
| EP-4592308-A1 | CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2025-07-30 | — | — | EP | disclosed |
| US-12371454-B2 | Cyclic peptide compound having Kras inhibitory action | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2025-07-29 | — | — | US | disclosed |
| US-20250230193-A1 | CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS | CHUGAI PHARMACEUTICAL CO LTD (JP) | 2025-07-17 | — | — | US | disclosed |
| CN-120202211-A | Cyclic compounds having selective KRAS inhibition over HRAS and NRAS | 中外制药株式会社 | 2025-06-24 | — | — | CN | disclosed |
| CN-120192216-A | Preparation method and application of trifluoromethyl alcohol compound | 深圳华润九新药业有限公司 | 2025-06-24 | — | — | CN | disclosed |
| US-20250197450-A1 | METHOD FOR PRODUCING N-ALKYL AMINO ACID AND PEPTIDE INCLUDING N-ALKYL AMINO ACID | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2025-06-19 | — | — | US | disclosed |
| US-20250179043-A1 | PROCESSES FOR THE PREPARATION OF N-(1-METHYLCYCLOPROPYL)-2-(3-PYRIDINYL)-2H-INDAZOLE-4-CARBOXAMIDE AND INTERMEDIATES THEREOF | FMC CORP (US) | 2025-06-05 | — | — | US | disclosed |
| CN-120082281-A | Preparation method of two-dimensional porous double transition metal oxide composite self-repairing noise-reducing anticorrosive coating | 中国海洋大学 | 2025-06-03 | — | — | CN | disclosed |
| US-20250163010-A1 | PROCESSES FOR THE PREPARATION OF N-(1-METHYLCYCLOPROPYL)-2-(3-PYRIDINYL)-2H-INDAZOLE-4-CARBOXAMIDE AND INTERMEDIATES THEREOF | FMC CORP (US) | 2025-05-22 | — | — | US | disclosed |
| US-20250154124-A1 | PROCESSES FOR THE PREPARATION OF N-(1-METHYLCYCLOPROPYL)-2-(3-PYRIDINYL)-2H-INDAZOLE-4-CARBOXAMIDE AND INTERMEDIATES THEREOF | FMC CORP (US) | 2025-05-15 | — | — | US | disclosed |
| CN-119731195-A | Cyclic compounds having selective inhibition of KRAS over HRAS and NRAS | 中外制药株式会社 | 2025-03-28 | — | — | CN | disclosed |
| EP-4522622-A1 | COMPOSITIONS USEFUL FOR MODULATING SPLICING | Skyhawk Therapeutics, Inc. (US) | 2025-03-19 | — | — | EP | disclosed |
| EP-4512818-A1 | CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS | Chugai Seiyaku Kabushiki Kaisha (JP) | 2025-02-26 | — | — | EP | disclosed |
| US-20250051394-A1 | CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2025-02-13 | — | — | US | disclosed |
| CN-114630835-B | Process for the preparation of peptide compounds comprising sterically bulky amino acids | 中外制药株式会社 | 2025-02-11 | — | — | CN | disclosed |
| WO-2025016391-A1 | THIAZOLE PYRAZINE COMPOUNDS AND USE THEREOF | 南京再明医药有限公司 | 2025-01-23 | — | — | WO | disclosed |
| US-20240400617-A1 | CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2024-12-05 | — | — | US | disclosed |
| CN-118807760-A | Heterojunction catalyst, preparation method and application | 中国科学技术大学 | 2024-10-22 | — | — | CN | disclosed |
| CN-118715213-A | Process for preparing N- (1-methylcyclopropyl) -2- (3-pyridinyl) -2H-indazole-4-carboxamide and intermediates thereof | FMC公司 | 2024-09-27 | — | — | CN | disclosed |
| CN-118715212-A | Preparation of N- (1-methylcyclopropyl) -2- (3-pyridinyl) -2H-indazole-4-carboxamide and intermediates thereof | FMC公司 | 2024-09-27 | — | — | CN | disclosed |
| CN-118679154-A | Preparation of N- (1-methylcyclopropyl) -2- (3-pyridinyl) -2H-indazole-4-carboxamide and intermediates thereof | FMC公司 | 2024-09-20 | — | — | CN | disclosed |
| EP-4414374-A1 | METHOD FOR PRODUCING N-ALKYL AMINO ACID AND PEPTIDE INCLUDING N-ALKYL AMINO ACID | Chugai Seiyaku Kabushiki Kaisha (JP) | 2024-08-14 | — | — | EP | disclosed |
| EP-3632892-B1 | METHOD FOR PRODUCING 3-ARYLPROPIONAMIDE COMPOUND | SUMITOMO CHEMICAL CO (JP) | 2024-07-31 | — | — | EP | disclosed |
| US-12012426-B2 | Tetradentate diaminodiphosphine ligand and transition metal complex, and method for manufacturing same and application for same | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2024-06-18 | — | — | US | disclosed |
| WO-2024117819-A1 | METHOD FOR MANUFACTURING NICKEL TRANSITION METAL COMPOSITE CATALYST ELECTRODE BY UTILIZING SINGLE-STEP ELECTRODEPOSITION AND DESALINATION COMBINED CATALYST ELECTRODE DEVICE | 경북대학교 산학협력단 | 2024-06-06 | — | — | WO | disclosed |
| CN-112654630-B | Tetradentate diaminodiphosphine ligands, transition metal complexes, methods for their production and use thereof | 高砂香料工业株式会社 | 2024-05-24 | — | — | CN | disclosed |
| US-20240166646-A1 | 1H-PYRROLO[2,3-B]PYRIDINE DERIVATIVES AS BCL-2 INHIBITORS FOR THE TREATMENT OF NEOPLASTIC AND AUTOIMMUNE DISEASES | NEWAVE PHARMACEUTICAL INC. | 2024-05-23 | — | — | US | disclosed |
| CN-118047735-A | Preparation method of pramoxine | 中国人民解放军空军军医大学 | 2024-05-17 | — | — | CN | disclosed |
| WO-2024101386-A1 | CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS | 中外製薬株式会社 | 2024-05-16 | — | — | WO | disclosed |
| US-20240158446-A1 | CYCLIC COMPOUND HAVING SELECTIVE INHIBITORY ACTION ON KRAS OVER HRAS AND NRAS | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2024-05-16 | — | — | US | disclosed |
| WO-2024101402-A1 | PHARMACEUTICAL COMPOSITION CONTAINING CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT AGAINST HRAS AND NRAS | 中外製薬株式会社 | 2024-05-16 | — | — | WO | disclosed |
| US-20240148821-A1 | PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2024-05-09 | — | — | US | disclosed |
| CN-114716466-B | Method for preparing chiral alpha-aminoboric acid/boric acid ester by nickel-catalyzed asymmetric hydrogen amidation | 南京大学 | 2024-03-19 | — | — | CN | disclosed |
| CN-117659291-A | Olefin and acrylic polymer and preparation method thereof | 中国石油天然气股份有限公司 | 2024-03-08 | — | — | CN | disclosed |
| CN-117586106-A | Method for synthesizing alkylaryl ether | 中国人民解放军空军军医大学 | 2024-02-23 | — | — | CN | disclosed |
| EP-4316503-A1 | PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2024-02-07 | — | — | EP | disclosed |
| EP-4309741-A1 | CYCLIC COMPOUND HAVING INHIBITORY EFFECT SELECTIVE FOR KRAS BUT NOT FOR HRAS AND NRAS | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2024-01-24 | — | — | EP | disclosed |
| CN-117303993-A | Nickel-catalyzed olefin asymmetric hydroarylation method and application | 南京大学 | 2023-12-29 | — | — | CN | disclosed |
| CN-117279933-A | Cyclic compounds having selective KRAS inhibition relative to HRAS and NRAS | 中外制药株式会社 | 2023-12-22 | — | — | CN | disclosed |
| CN-115155509-B | Preparation method of heavy metal ion immobilized separation column packing | 江苏大学 | 2023-12-15 | — | — | CN | disclosed |
| WO-2023220439-A1 | COMPOSITIONS USEFUL FOR MODULATING SPLICING | SKYHAWK THERAPEUTICS, INC. (US) | 2023-11-16 | — | — | WO | disclosed |
| WO-2023214576-A1 | CYCLIC COMPOUND HAVING SELECTIVE KRAS INHIBITORY EFFECT ON HRAS AND NRAS | 中外製薬株式会社 | 2023-11-09 | — | — | WO | disclosed |
| CN-114751993-B | Preparation method of cellulose nanocrystalline capable of being dried and redispersed | 陕西科技大学 | 2023-09-01 | — | — | CN | disclosed |
| WO-2023158771-A1 | THE PREPARATION OF N-(1-METHYLCYCLOPROPYL)-2-(3-PYRIDINYL)-2H-INDAZOLE-4-CARBOXAMIDE AND INTERMEDIATES THEREOF | FMC CORPORATION (US) | 2023-08-24 | — | — | WO | disclosed |
| WO-2023158769-A1 | PROCESSES FOR THE PREPARATION OF N-(1- METHYLCYCLOPROPYL)-2-(3 -PYRIDINYL)-2H- INDAZOLE-4-CARBOXAMIDE AND INTERMEDIATES THEREOF | FMC CORPORATION (US) | 2023-08-24 | — | — | WO | disclosed |
| WO-2023158770-A1 | THE PREPARATION OF N-(1-METHYLCYCLOPROPYL)-2-(3-PYRIDINYL)-2H-INDAZOLE-4-CARBOXAMIDE AND INTERMEDIATES THEREOF | FMC CORPORATION (US) | 2023-08-24 | — | — | WO | disclosed |
| WO-2023137675-A1 | USE OF NICKEL/KETONE DUAL-CATALYSIS SYSTEM IN CROSS-COUPLING REACTION OF ARYL HALIDE AND SODIUM ARYLSULFINATE | 苏州大学 | 2023-07-27 | — | — | WO | disclosed |
| WO-2023137675-A1 | USE OF NICKEL/KETONE DUAL-CATALYSIS SYSTEM IN CROSS-COUPLING REACTION OF ARYL HALIDE AND SODIUM ARYLSULFINATE | 苏州大学 | 2023-07-27 | — | — | WO | disclosed |
| US-20230219983-A1 | TETRADENTATE DIAMINODIPHOSPHINE LIGAND AND TRANSITION METAL COMPLEX, AND METHOD FOR MANUFACTURING SAME AND APPLICATION FOR SAME | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2023-07-13 | — | — | US | disclosed |
| CN-116410213-A | Method for synthesizing 3-carbon-1-boron-based ring compound | 武汉大学 | 2023-07-11 | — | — | CN | disclosed |
| WO-2023127869-A1 | METHOD FOR PRODUCING N-ALKYL AMINO ACID AND PEPTIDE INCLUDING N-ALKYL AMINO ACID | 中外製薬株式会社 | 2023-07-06 | — | — | WO | disclosed |
| CN-114478371-B | Application of nickel/ketone double-catalysis system in cross-coupling reaction of halogenated aromatic hydrocarbon and aryl sodium sulfinate | 苏州大学 | 2023-07-04 | — | — | CN | disclosed |
| CN-114478371-B | Application of nickel/ketone double-catalysis system in cross-coupling reaction of halogenated aromatic hydrocarbon and aryl sodium sulfinate | 苏州大学 | 2023-07-04 | — | — | CN | disclosed |
| US-20230151060-A1 | CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2023-05-18 | — | — | US | disclosed |
| CN-110799490-B | 3-arylpropionamide compound and method for producing 3-arylpropionate compound | 住友化学株式会社 | 2023-05-02 | — | — | CN | disclosed |
| US-11639362-B2 | Tetradentate diaminodiphosphine ligand and transition metal complex, and method for manufacturing same and application for same | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2023-05-02 | — | — | US | disclosed |
| US-20230096766-A1 | AMINO ACID HAVING FUNCTIONAL GROUP CAPABLE OF INTERMOLECULAR HYDROGEN BONDING, PEPTIDE COMPOUND CONTAINING SAME AND METHOD FOR PRODUCTION THEREOF | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2023-03-30 | — | — | US | disclosed |
| WO-2022234853-A1 | CYCLIC COMPOUND HAVING INHIBITORY EFFECT SELECTIVE FOR KRAS BUT NOT FOR HRAS AND NRAS | 中外製薬株式会社 | 2022-11-10 | — | — | WO | disclosed |
| WO-2022234852-A1 | PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND | 中外製薬株式会社 | 2022-11-10 | — | — | WO | disclosed |
| CN-115155509-A | Preparation method of heavy metal ion immobilized separation column filler | 江苏大学 | 2022-10-11 | — | — | CN | disclosed |
| EP-4043478-A1 | CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITING ACTION | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2022-08-17 | — | — | EP | disclosed |
| CN-114907247-A | Preparation method of pyrrolidine intermediate and pyrrolidine salt compound | 上海陶术生物科技有限公司 | 2022-08-16 | — | — | CN | disclosed |
| CN-114751993-A | Preparation method of cellulose nanocrystal capable of being dried and redispersed | 陕西科技大学 | 2022-07-15 | — | — | CN | disclosed |
| CN-114716466-A | Method for preparing chiral alpha-amino boric acid/boric acid ester through nickel-catalyzed asymmetric hydroamidation | 南京大学 | 2022-07-08 | — | — | CN | disclosed |
| CN-114729006-A | Cyclic peptide compounds having Kras inhibitory activity | 中外制药株式会社 | 2022-07-08 | — | — | CN | disclosed |
| CN-113754689-B | Nickel-catalyzed asymmetric hydroamination method for olefin | 南京大学 | 2022-07-08 | — | — | CN | disclosed |
| EP-3750896-B1 | CHIRAL TETRADENTATE LIGAND, METHOD FOR PRODUCING SAME AND TRANSITION METAL COMPLEX OF SAID CHIRAL TETRADENTATE LIGAND | TAKASAGO PERFUMERY CO LTD (JP) | 2022-06-29 | — | — | EP | disclosed |
| CN-105669365-B | Aryl or heteroaryl compound containing difluoroalkyl substitution, preparation method and application | 中国科学院上海有机化学研究所 | 2022-06-21 | — | — | CN | disclosed |
| CN-114630835-A | Process for the preparation of peptide compounds comprising sterically bulky amino acids | 中外制药株式会社 | 2022-06-14 | — | — | CN | disclosed |
| CN-112939750-B | Method for transferring asymmetric functionalization by nickel-hydrogen catalysis olefin promoted by ligand relay strategy | 南京大学 | 2022-05-17 | — | — | CN | disclosed |
| CN-114478371-A | Application of nickel/ketone double-catalysis system in cross-coupling reaction of halogenated aromatic hydrocarbon and sodium arylsulfinate | 苏州大学 | 2022-05-13 | — | — | CN | disclosed |
| CN-114478371-A | Application of nickel/ketone double-catalysis system in cross-coupling reaction of halogenated aromatic hydrocarbon and sodium arylsulfinate | 苏州大学 | 2022-05-13 | — | — | CN | disclosed |
| US-11316146-B2 | Redox and ion-adsorption electrodes and energy storage devices | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2022-04-26 | — | — | US | disclosed |
| CN-112679290-B | Nickel-catalyzed asymmetric hydrogen alkynylation method for olefins and application of nickel-catalyzed asymmetric hydrogen alkynylation method in preparation of AMG837 | 南京大学 | 2022-03-15 | — | — | CN | disclosed |
| CN-113754689-A | Nickel-catalyzed asymmetric hydroamination method for olefin | 南京大学 | 2021-12-07 | — | — | CN | disclosed |
| CN-112538098-B | Alpha-sulfonic acid-beta-diimine nickel complex, preparation method and application thereof in catalyzing olefin polymerization | 中山大学 | 2021-11-26 | — | — | CN | disclosed |
| EP-3896056-A1 | AMINO ACID HAVING FUNCTIONAL GROUP CAPABLE OF INTERMOLECULAR HYDROGEN BONDING, PEPTIDE COMPOUND CONTAINING SAME AND METHOD FOR PRODUCTION THEREOF | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2021-10-20 | — | — | EP | disclosed |
| CN-110305171-B | Preparation and application of mixed nickel (II) complex containing bisoxazoline-derived nitrogen heterocyclic carbene ligand and phosphite ligand | 苏州大学 | 2021-09-28 | — | — | CN | disclosed |
| EP-3848378-A1 | TETRADENTATE DIAMINODIPHOSPHINE LIGAND AND TRANSITION METAL COMPLEX, AND METHOD FOR MANUFACTURING SAME AND APPLICATION FOR SAME | Takasago International Corporation (JP) | 2021-07-14 | — | — | EP | disclosed |
| CN-112939750-A | Method for transferring asymmetric functionalization by nickel-hydrogen catalysis olefin promoted by ligand relay strategy | 南京大学 | 2021-06-11 | — | — | CN | disclosed |
| US-11028056-B2 | Method for producing 3-arylpropionamide compound and 3-arylpropionic acid ester compound | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2021-06-08 | — | — | US | disclosed |
| CN-112679290-A | Nickel-catalyzed asymmetric hydrogen alkynylation method for olefins and application of nickel-catalyzed asymmetric hydrogen alkynylation method in preparation of AMG837 | 南京大学 | 2021-04-20 | — | — | CN | disclosed |
| CN-112654630-A | Tetradentate diamino diphosphine ligand, transition metal complex, their production method and use | 高砂香料工业株式会社 | 2021-04-13 | — | — | CN | disclosed |
| CN-112538098-A | Alpha-sulfonic acid-beta-diimine nickel complex, preparation method and application thereof in catalyzing olefin polymerization | 中山大学 | 2021-03-23 | — | — | CN | disclosed |
| EP-3438113-B1 | TETRADENTATE LIGAND, AND PRODUCTION METHOD THEREFOR, SYNTHETIC INTERMEDIATE THEREOF, AND TRANSITION METAL COMPLEX THEREOF | TAKASAGO PERFUMERY CO LTD (JP) | 2021-02-17 | — | — | EP | disclosed |
| WO-2021018157-A1 | PREPARATION AND APPLICATION OF MIXED-LIGAND NICKEL(II) COMPLEX CONTAINING BISOXAZOLINE-DERIVED NITROGEN HETEROCYCLIC CARBENE LIGAND AND PHOSPHITE LIGAND | 苏州大学 | 2021-02-04 | — | — | WO | disclosed |
| EP-3750896-A1 | CHIRAL TETRADENTATE LIGAND, METHOD FOR PRODUCING SAME AND TRANSITION METAL COMPLEX OF SAID CHIRAL TETRADENTATE LIGAND | Takasago International Corporation (JP) | 2020-12-16 | — | — | EP | disclosed |
| EP-3747071-A1 | REDOX AND ION-ADSORBTION ELECTRODES AND ENERGY STORAGE DEVICES | The Regents of the University of California (US) | 2020-12-09 | — | — | EP | disclosed |
| CN-106278847-B | Compound containing fluoroalkyl, preparation method and application thereof | 中国科学院上海有机化学研究所 | 2020-12-08 | — | — | CN | disclosed |
| CN-112005408-A | Redox and ion adsorption electrode and energy storage device | 加利福尼亚大学董事会 | 2020-11-27 | — | — | CN | disclosed |
| US-20200369700-A1 | CHIRAL TETRADENTATE LIGAND, METHOD FOR PRODUCING SAME AND TRANSITION METAL COMPLEX OF SAID CHIRAL TETRADENTATE LIGAND | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2020-11-26 | — | — | US | disclosed |
| US-20200266425-A1 | REDOX AND ION-ADSORPTION ELECTRODES AND ENERGY STORAGE DEVICES | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA | 2020-08-20 | — | — | US | disclosed |
| US-10693126-B2 | Redox and ion-adsorption electrodes and energy storage devices | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2020-06-23 | — | — | US | disclosed |
| WO-2020122182-A1 | AMINO ACID HAVING FUNCTIONAL GROUP CAPABLE OF INTERMOLECULAR HYDROGEN BONDING, PEPTIDE COMPOUND CONTAINING SAME AND METHOD FOR PRODUCTION THEREOF | 中外製薬株式会社 | 2020-06-18 | — | — | WO | disclosed |
| US-20200165209-A1 | METHOD FOR PRODUCING 3-ARYLPROPIONAMIDE COMPOUND AND 3-ARYLPROPIONIC ACID ESTER COMPOUND | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2020-05-28 | — | — | US | disclosed |
| EP-3632892-A1 | METHOD FOR PRODUCING 3-ARYLPROPIONAMIDE COMPOUND AND 3-ARYLPROPIONIC ACID ESTER COMPOUND | Sumitomo Chemical Company, Limited (JP) | 2020-04-08 | — | — | EP | disclosed |
| CN-110878012-A | Synthetic method of E-type methyl styrene compound | 南京大学 | 2020-03-13 | — | — | CN | disclosed |
| CN-110799490-A | Process for producing 3-arylpropionamide compound and process for producing 3-arylpropionate compound | 住友化学株式会社 | 2020-02-14 | — | — | CN | disclosed |
| US-10550141-B2 | Tetradentate ligand, and production method therefor, synthetic intermediate thereof, and transition metal complex thereof | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2020-02-04 | — | — | US | disclosed |
| CN-108872208-B | Ammonia catalytic luminescence sensing material | 北京联合大学 | 2019-12-10 | — | — | CN | disclosed |
| US-10462908-B2 | Conductive patterns and methods of using them | ALPHA ASSEMBLY SOLUTIONS INC. (US) | 2019-10-29 | — | — | US | disclosed |
| US-20190237752-A1 | REDOX AND ION-ADSORBTION ELECTRODES AND ENERGY STORAGE DEVICES | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA | 2019-08-01 | — | — | US | disclosed |
| US-20190127407-A1 | TETRADENTATE LIGAND, AND PRODUCTION METHOD THEREFOR, SYNTHETIC INTERMEDIATE THEREOF, AND TRANSITION METAL COMPLEX THEREOF | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2019-05-02 | — | — | US | disclosed |
| EP-3438113-A1 | TETRADENTATE LIGAND, AND PRODUCTION METHOD THEREFOR, SYNTHETIC INTERMEDIATE THEREOF, AND TRANSITION METAL COMPLEX THEREOF | Takasago International Corporation (JP) | 2019-02-06 | — | — | EP | disclosed |
| US-10193139-B1 | Redox and ion-adsorbtion electrodes and energy storage devices | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2019-01-29 | — | — | US | disclosed |
| EP-3269699-A1 | CATALYTIC CARBOXYLATION OF ACTIVATED ALKANES AND/OR OLEFINS | Fundació Institut Català D'investigació Quimica (ES) | 2018-01-17 | — | — | EP | disclosed |
| EP-2064000-B1 | SOLVENT SYSTEMS FOR METALS AND INKS | ALPHA ASSEMBLY SOLUTIONS INC (US) | 2018-01-17 | — | — | EP | disclosed |
| US-20170271637-A1 | METHOD OF MANUFACTURING POROUS POLYMER MEMBRANE USING WATER PRESSURE AND BATTERY SEPARATOR COMPRISING POROUS POLYMER MEMBRANE MANUFACTURED BY THE METHOD | SANGMYUNG UNIVERSITY SEOUL INDUSTRY ACADEMY COOPERATION FOUNDATION (KR) | 2017-09-21 | — | — | US | disclosed |
| EP-2937355-B1 | PHOSPHORUS COMPOUND AND TRANSITION METAL COMPLEX OF THE SAME | TAKASAGO PERFUMERY CO LTD (JP) | 2017-06-28 | — | — | EP | disclosed |
| US-20170164484-A1 | Conductive Patterns and Methods of Using Them | CITIBANK, N.A. | 2017-06-08 | — | — | US | disclosed |
| US-9615463-B2 | Method for producing a high-aspect ratio conductive pattern on a substrate | CITIBANK, N.A. | 2017-04-04 | — | — | US | disclosed |
| EP-2174324-B1 | METHOD OF MANUFACTURING PRINTED CIRCUIT BOARD | ALPHA METALS (US) | 2017-01-11 | — | — | EP | disclosed |
| US-9476138-B2 | Composite plating liquid | SHINKO ELECTRIC INDUSTRIES CO., LTD (JP) | 2016-10-25 | — | — | US | disclosed |
| US-9416148-B2 | Phosphorus compound and transition metal complex of the same | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2016-08-16 | — | — | US | disclosed |
| US-9217088-B2 | Particles and inks and films using them | ALPHA METALS, INC. (US) | 2015-12-22 | — | — | US | disclosed |
| EP-2942350-A1 | SPIRO-OXINDOLE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS | Xenon Pharmaceuticals Inc. (CA) | 2015-11-11 | — | — | EP | disclosed |
| US-20150307531-A1 | PHOSPHORUS COMPOUND AND TRANSITION METAL COMPLEX OF THE SAME | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2015-10-29 | — | — | US | disclosed |
| EP-2937355-A1 | PHOSPHORUS COMPOUND AND TRANSITION METAL COMPLEX OF THE SAME | Takasago International Corporation (JP) | 2015-10-28 | — | — | EP | disclosed |
| EP-2350090-B1 | SPIRO-OXINDOLE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS | XENON PHARMACEUTICALS INC (CA) | 2015-06-03 | — | — | EP | disclosed |
| US-9011734-B2 | Ligand exchange thermochromic, (LETC), systems | PLEOTINT, L.L.C. (US) | 2015-04-21 | — | — | US | disclosed |
| US-20150065738-A1 | PHOSPHOROUS COMPOUND AND TRANSITION METAL COMPLEX THEREOF | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2015-03-05 | — | — | US | disclosed |
| EP-2842959-A1 | Phosphorous compound and transition metal complex thereof | Takasago International Corporation (JP) | 2015-03-04 | — | — | EP | disclosed |
| US-8916580-B2 | Spiro-oxindole compounds and their use as therapeutic agents | XENON PHARMACEUTICALS INC. (CA) | 2014-12-23 | — | — | US | disclosed |
| EP-1853519-B1 | ZERO VALENT METAL COMPOSITE, MANUFACTURING, SYSTEM AND METHOD USING THEREOF, FOR CATALYTICALLY TREATING CONTAMINATED WATER | YEDA RES & DEV (IL) | 2014-09-03 | — | — | EP | disclosed |
| US-20140186524-A1 | SOLVENT SYSTEMS FOR METALS AND INKS | ALPHA METALS, INC. (US) | 2014-07-03 | — | — | US | disclosed |
| EP-2380688-B1 | Particles and Inks and Films Using Them | ALPHA METALS (US) | 2014-06-04 | — | — | EP | disclosed |
| US-8598062-B2 | Zero valent metal composite, manufacturing, system and method using thereof, for catalytically treating contaminated water | YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) | 2013-12-03 | — | — | US | disclosed |
| US-8597548-B2 | Solvent systems for metals and inks | ALPHA METALS, INC. (US) | 2013-12-03 | — | — | US | disclosed |
| EP-2066470-B1 | METHODS OF PREPARING SILVER PARTICLES, SILVER PARTICLE INKS AND SILVER PARTICLE FILMS | FRY METALS INC (US) | 2013-10-09 | — | — | EP | disclosed |
| US-20130252962-A1 | SPIRO-OXINDOLE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS | XENON PHARMACEUTICALS INC (CA) | 2013-09-26 | — | — | US | disclosed |
| EP-2082005-B9 | LIGAND EXCHANGE THERMOCHROMIC, (LETC), SYSTEMS | PLEOTINT LLC (US) | 2013-05-22 | — | — | EP | disclosed |
| US-20130123098-A1 | ZERO VALENT METAL COMPOSITE, MANUFACTURING, SYSTEM AND METHOD USING THEREOF, FOR CATALYTICALLY TREATING CONTAMINATED WATER | YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) | 2013-05-16 | — | — | US | disclosed |
| US-8431045-B2 | Ligand exchange thermochromic systems and high ε ligands for same | PLEOTINT, L.L.C. (US) | 2013-04-30 | — | — | US | disclosed |
| US-8415370-B2 | Spiro-oxindole compounds and their uses as therapeutic agents | XENON PHARMACEUTICALS INC. (CA) | 2013-04-09 | — | — | US | disclosed |
| US-8366940-B2 | Zero valent metal composite, manufacturing, system and method using thereof, for catalytically treating contaminated water | YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) | 2013-02-05 | — | — | US | disclosed |
| US-20120292581-A1 | LIGAND EXCHANGE THERMOCHROMIC SYSTEMS AND HIGH E LIGANDS FOR SAME | PLEOTINT, LLC (US) | 2012-11-22 | — | — | US | disclosed |
| US-20120295897-A1 | SPIRO-OXINDOLE COMPOUNDS AND THEIR USES AS THERAPEUTIC AGENTS | XENON PHARMACEUTICALS INC. (CA) | 2012-11-22 | — | — | US | disclosed |
| US-8263606-B2 | Spiro-oxindole compounds and their use as therapeutic agents | XENON PHARMACEUTICALS INC. (CA) | 2012-09-11 | — | — | US | disclosed |
| US-20120216997-A1 | COMPOSITE PLATING LIQUID | SHINSHU UNIVERSITY (JP) | 2012-08-30 | — | — | US | disclosed |
| EP-2082005-B1 | LIGAND EXCHANGE THERMOCHROMIC, (LETC), SYSTEMS | PLEOTINT LLC (US) | 2012-08-01 | — | — | EP | disclosed |
| US-8182718-B2 | Ligand exchange thermochromic systems and high ε ligands for same | PLEOTINT, L.L.C. (US) | 2012-05-22 | — | — | US | disclosed |
| EP-2436750-A2 | Ligand exchange thermochromic, (LETC), systems | Pleotint, L.L.C. (US) | 2012-04-04 | — | — | EP | disclosed |
| EP-2434000-A2 | Ligand exchange thermochromic, (LETC), systems | Pleotint, L.L.C. (US) | 2012-03-28 | — | — | EP | disclosed |
| US-20120001134-A1 | LIGAND EXCHANGE THERMOCHROMIC, (LETC), SYSTEMS | PLEOTINT, LLC (US) | 2012-01-05 | — | — | US | disclosed |
| US-20110318478-A1 | PARTICLES AND INKS AND FILMS USING THEM | CITIBANK, N.A. | 2011-12-29 | — | — | US | disclosed |
| EP-2380688-A1 | Particles and Inks and Films Using Them | Fry's Metals, Inc. (US) | 2011-10-26 | — | — | EP | disclosed |
| US-20110236760-A1 | Electrode for non-aqueous electrolyte secondary battery, method for producing the same, and non-aqueous electrolyte secondary battery | DAI NIPPON PRINTING CO., LTD. (JP) | 2011-09-29 | — | — | US | disclosed |
| US-20110229767-A1 | Electrode for non-aqueous electrolyte secondary battery, method for producing the same, and non-aqueous electrolyte secondary battery | DAI NIPPON PRINTING CO., LTD. (JP) | 2011-09-22 | — | — | US | disclosed |
| US-8018639-B2 | Ligand exchange thermochromic, (LETC), systems | PLEOTINT, L.L.C. (US) | 2011-09-13 | — | — | US | disclosed |
| US-7968008-B2 | Particles and inks and films using them | FRY'S METALS, INC. (US) | 2011-06-28 | — | — | US | disclosed |
| EP-1988998-B1 | IMPROVED PROCESS FOR PRODUCING NICKEL(0)-PHOSPHORUS LIGAND COMPLEXES | BASF SE (DE) | 2011-06-15 | — | — | EP | disclosed |
| EP-1716105-B1 | METHOD FOR PRODUCING LINEAR PENTENENITRILE | BASF SE (DE) | 2011-04-27 | — | — | EP | disclosed |
| US-20100137299-A1 | SPIRO-OXINDOLE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS | XENON PHARMACEUTICALS INC. (CA) | 2010-06-03 | — | — | US | disclosed |
| US-7705171-B2 | Process for producing nickel(0)-phosphorus ligand complexes | BASF AKTIENGESELLSCHAFT (DE) | 2010-04-27 | — | — | US | disclosed |
| US-7700795-B2 | Use of azeotropically dried nickel(ii) halogenides | BASF AKTIENGESELLSCHAFT (DE) | 2010-04-20 | — | — | US | disclosed |
| EP-2174324-A1 | CONDUCTIVE PATTERNS AND METHODS OF USING THEM | Fry's Metals, Inc. (US) | 2010-04-14 | — | — | EP | disclosed |
| US-20090283728-A1 | LIGAND EXCHANGE THERMOCHROMIC, (LETC), SYSTEMS | PLEOTINT, LLC (US) | 2009-11-19 | — | — | US | disclosed |
| EP-2082005-A1 | LIGAND EXCHANGE THERMOCHROMIC, (LETC), SYSTEMS | Pleotint, L.L.C. (US) | 2009-07-29 | — | — | EP | disclosed |
| EP-2066470-A1 | PARTICLES AND INKS AND FILMS USING THEM | Fry's Metals, Inc. (US) | 2009-06-10 | — | — | EP | disclosed |
| EP-2064000-A2 | SOLVENT SYSTEMS FOR METALS AND INKS | Fry's Metals, Inc. (US) | 2009-06-03 | — | — | EP | disclosed |
| US-7542196-B2 | Ligand exchange thermochromic, (LETC), systems | PLEOTINT, L.L.C. (US) | 2009-06-02 | — | — | US | disclosed |
| US-7538931-B2 | Ligand exchange thermochromic systems containing exchange metals | PLEOTINT, L.L.C. (US) | 2009-05-26 | — | — | US | disclosed |
| US-20090127208-A1 | ZERO VALENT METAL COMPOSITE, MANUFACTURING, SYSTEM AND METHOD USING THEREOF, FOR CATALYTICALLY TREATING CONTAMINATED WATER | YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) | 2009-05-21 | — | — | US | disclosed |
| WO-2009020464-A9 | CONDUCTIVE PATTERNS AND METHODS OF USING THEM | FRY METALS INC (US) | 2009-04-30 | — | — | WO | disclosed |
| US-7525717-B2 | reversible; laminated; transition metal ion coordinated with a high epsilon ligand and a low epsilon ligand; polymer; separator; variable light transmission windows; polyvinyl butyral; nickel or cobalt iodide ligands; diol, triol or polyol ligands | PLEOTINT, L.L.C. (US) | 2009-04-28 | — | — | US | disclosed |
| US-20090054671-A1 | PROCESS FOR PRODUCING NICKEL(0)-PHOSPHORUS LIGAND COMPLEXES | BASF SE (DE) | 2009-02-26 | — | — | US | disclosed |
| WO-2009020464-A1 | CONDUCTIVE PATTERNS AND METHODS OF USING THEM | FRY'S METALS, INC. (US) | 2009-02-12 | — | — | WO | disclosed |
| US-20080281120-A1 | Method for Producing Linear Pentenenitrile | BASF AKTIENGESELLSCHAFT (DE) | 2008-11-13 | — | — | US | disclosed |
| EP-1988998-A1 | IMPROVED PROCESS FOR PRODUCING NICKEL(0)-PHOSPHORUS LIGAND COMPLEXES | BASF SE (DE) | 2008-11-12 | — | — | EP | disclosed |
| US-20080145560-A1 | Used with capped metal (silver) particles to provide a dispersion that may be used to print conductive lines | CITIBANK, N.A. | 2008-06-19 | — | — | US | disclosed |
| US-20080137316-A1 | CONDUCTIVE PATTERNS AND METHODS OF USING THEM | CITIBANK, N.A. | 2008-06-12 | — | — | US | disclosed |
| US-20080105851-A1 | Exhibiting a reversible change in absorbance of electromagnetic radiation as the temperature of the system is reversibly changed; comprising a transition metal ion and a ligand | PLEOTINT, LLC (US) | 2008-05-08 | — | — | US | disclosed |
| US-20080106781-A1 | LIGAND EXCHANGE THERMOCHROMIC SYSTEMS CONTAINING EXCHANGE METALS | PLEOTINT, LLC (US) | 2008-05-08 | — | — | US | disclosed |
| US-20080100903-A1 | MULTI-LAYER LIGAND EXCHANGE THERMOCHROMIC SYSTEMS | PLEOTINT, LLC (US) | 2008-05-01 | — | — | US | disclosed |
| US-20080100902-A1 | LIGAND EXCHANGE THERMOCHROMIC, (LETC), SYSTEMS | PLEOTINT, LLC (US) | 2008-05-01 | — | — | US | disclosed |
| WO-2008036752-A2 | SOLVENT SYSTEMS FOR METALS AND INKS | FRY'S METALS, INC. (US) | 2008-03-27 | — | — | WO | disclosed |
| WO-2008028128-A1 | LIGAND EXCHANGE THERMOCHROMIC, (LETC), SYSTEMS | PLEOTINT, L.L.C. (US) | 2008-03-06 | — | — | WO | disclosed |
| US-20080032047-A1 | PARTICLES AND INKS AND FILMS USING THEM | CITIBANK, N.A. | 2008-02-07 | — | — | US | disclosed |
| WO-2008017062-A1 | PARTICLES AND INKS AND FILMS USING THEM | FRY'S METALS, INC. (US) | 2008-02-07 | — | — | WO | disclosed |
| EP-1853519-A2 | ZERO VALENT METAL COMPOSITE, MANUFACTURING, SYSTEM AND METHOD USING THEREOF, FOR CATALYTICALLY TREATING CONTAMINATED WATER | YEDA RESEARCH AND DEVELOPMENT CO., LTD. (IL) | 2007-11-14 | — | — | EP | disclosed |
| WO-2007096274-A1 | IMPROVED PROCESS FOR PRODUCING NICKEL(0)-PHOSPHORUS LIGAND COMPLEXES | BASF SE (DE) | 2007-08-30 | — | — | WO | disclosed |
| EP-1825914-A1 | Improved process for the preparation of nickel(0) - phosphorus ligand - complexes | BASF AKTIENGESELLSCHAFT (DE) | 2007-08-29 | — | — | EP | disclosed |
| US-20070083057-A1 | Method for the production of nickel(0)-phosphorous ligand complexes | BASF AKTIENGESELLSCHAFT (DE) | 2007-04-12 | — | — | US | disclosed |
| US-20070073071-A1 | Use of azeotropically dried nickel(ii) halogenides | BASF AKTIENGESELLSCHAFT (DE) | 2007-03-29 | — | — | US | disclosed |
| EP-1114028-B1 | AZA-BICYCLES WHICH MODULATE THE INHIBITION OF CELL ADHESION | AVENTIS PHARMA LTD (GB) | 2006-11-29 | — | — | EP | disclosed |
| EP-1716105-A1 | METHOD FOR PRODUCING LINEAR PENTENENITRILE | BASF AKTIENGESELLSCHAFT (DE) | 2006-11-02 | — | — | EP | disclosed |
| EP-1270582-B1 | TRIPHENYLPHOSPHINE DERIVATIVES, PALLADIUM OR NICKEL COMPLEXES THEREOF, AND PROCESS FOR PREPARING BIARYL DERIVATIVES | MITSUBISHI RAYON CO (JP) | 2006-08-30 | — | — | EP | disclosed |
| EP-1682270-A2 | METHOD FOR THE PRODUCTION OF NICKEL(0)-PHOSPHOROUS LIGAND COMPLEXES | BASF AKTIENGESELLSCHAFT (DE) | 2006-07-26 | — | — | EP | disclosed |
| EP-1682561-A1 | USE OF AZEOTROPICALLY DRIED NICKEL(II) HALOGENIDES | BASF AKTIENGESELLSCHAFT (DE) | 2006-07-26 | — | — | EP | disclosed |
| WO-2006072944-A2 | ZERO VALENT METAL COMPOSITE FOR CATALYTICALY TREATING CONTAMINATED WATER | YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) | 2006-07-13 | — | — | WO | disclosed |
| WO-2005073174-A1 | METHOD FOR PRODUCING LINEAR PENTENENITRILE | BASF AKTIENGESELLSCHAFT (DE) | 2005-08-11 | — | — | WO | disclosed |
| WO-2005042549-A1 | USE OF AZEOTROPICALLY DRIED NICKEL(II) HALOGENIDES | BASF AKTIENGESELLSCHAFT (DE) | 2005-05-12 | — | — | WO | disclosed |
| WO-2005042157-A2 | METHOD FOR THE PRODUCTION OF NICKEL(0)-PHOSPHOROUS LIGAND COMPLEXES | BASF AKTIENGESELLSCHAFT (DE) | 2005-05-12 | — | — | WO | disclosed |
| US-6693210-B2 | USING PALLADIUM, NICKEL PHOSPHINE COMPLEX AS CATALYSTS | MITSUBISHI RAYON CO., LTD. (JP) | 2004-02-17 | — | — | US | disclosed |
| US-20030220307-A1 | Remedial agent for osteoporosis | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2003-11-27 | — | — | US | disclosed |
| US-6608084-B1 | Treatment of human or non-human animal patient suffering from, or subject to, condition which can be ameliorated by administration of inhibitor of alpha 4 beta 1 mediated cell adhesion | AVENTIS PHARMA LTD. (GB) | 2003-08-19 | — | — | US | disclosed |
| EP-1314427-A1 | REMEDIAL AGENT FOR OSTEOPOROSIS | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2003-05-28 | — | — | EP | disclosed |
| US-20030065208-A1 | Using palladium, nickel phosphine complex as catalysts | MITSUBISHI RAYON CO., LTD. (JP) | 2003-04-03 | — | — | US | disclosed |
| EP-1270582-A1 | TRIPHENYLPHOSPHINE DERIVATIVE, PRODUCTION PROCESS THEREFOR, PALLADIUM COMPLEX THEREOF, AND PROCESS FOR PRODUCING BIARYL DERIVATIVE | Mitsubishi Rayon Co., Ltd. (JP) | 2003-01-02 | — | — | EP | disclosed |
| EP-1114028-A1 | AZA-BICYCLES WHICH MODULATE THE INHIBITION OF CELL ADHESION | Aventis Pharma Limited (GB) | 2001-07-11 | — | — | EP | disclosed |
| WO-2000015612-A1 | AZA-BICYCLES WHICH MODULATE THE INHIBITION OF CELL ADHESION | AVENTIS PHARMA LIMITED (GB) | 2000-03-23 | — | — | WO | disclosed |
| US-4960549-A | EXTRUDING FOAMABLE COMPOSITION INTO CONFINED EXPANSION ZONE, EXPANDING AND COOLING | AMOCO CORPORATION (US) | 1990-10-02 | — | — | US | disclosed |
| US-4412942-A | POLYACETYLENE; TOSYLMETHYL ISOCYANIDE; ALKALI METAL, ALKALI METAL AMIDE OR LEWIS ACID DOPANT | BASF AKTIENGESELLSCHAFT (DE) | 1983-11-01 | — | — | US | disclosed |
| EP-0026154-B1 | PROCESS FOR PREPARING 4,4'-DINITROSTILBENE-2,2'-DISULFONIC ACID AND ITS SALTS AND ITS USE | CIBA-GEIGY AG (CH) | 1983-06-29 | — | — | EP | disclosed |
| EP-0070450-A1 | Process for the preparation of electrically conductive polymers, and their use in electrotechnics and as antistatics in polymers | BASF Aktiengesellschaft (DE) | 1983-01-26 | — | — | EP | disclosed |
| EP-0064703-A1 | Process for the preparation of electrically conducting polymers, and their use in the electrotechnique and for the antistatic sizing of plastics | BASF Aktiengesellschaft (DE) | 1982-11-17 | — | — | EP | disclosed |
| EP-0059325-A1 | Process for the manufacture of electrically conductive polymers and their use in the electro-technique and in rendering plastics antistatic | BASF Aktiengesellschaft (DE) | 1982-09-08 | — | — | EP | disclosed |
| EP-0041784-A1 | Oxidation of substituted aromatic compounds to aromatic carboxylic acids | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1981-12-16 | — | — | EP | disclosed |
| EP-0034413-A1 | Process for the preparation of diphenylether carboxylic acids | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1981-08-26 | — | — | EP | disclosed |
| US-4268699-A | Hydroalkylation using nickel-ruthenium catalyst on zeolite type support | PHILLIPS PETROLEUM COMPANY (US) | 1981-05-19 | — | — | US | disclosed |
| EP-0026154-A1 | Process for preparing 4,4'-dinitrostilbene-2,2'-disulfonic acid and its salts and its use | CIBA-GEIGY AG (CH) | 1981-04-01 | — | — | EP | disclosed |
| US-4174302-A | FROM MONOCYCLIC AROMATICS, RUTHENIUM, NICKEL AND ACTIVE CLAY OR ALUMINA-SILICA SUPPORT | PHILLIPS PETROLEUM COMPANY (US) | 1979-11-13 | — | — | US | disclosed |
| US-4122261-A | Polycyclic iminoisoindoline chelates | STERLING DRUG INC. (US) | 1978-10-24 | — | — | US | disclosed |
| US-4115463-A | RUTHENIUM-NICKEL ON CLAY OR ALUMINA-SILICA SUPPORT | PHILLIPS PETROLEUM COMPANY (US) | 1978-09-19 | — | — | US | disclosed |
| US-4066653-A | 1-IMINO-3-(4-IMINO-5-THIAZOLIDINYLIDENE)ISOINDOLINES | STERLING DRUG INC. (US) | 1978-01-03 | — | — | US | disclosed |
| US-3993658-A | Thiazolidinylidene-isoindolines | STERLING DRUG INC. (US) | 1976-11-23 | — | — | US | disclosed |
| US-3960934-A | METAL HALIDE CATALYST | ROHM GMBH (DT) | 1976-06-01 | — | — | US | disclosed |
| US-3960934-A | METAL HALIDE CATALYST | ROHM GMBH (DT) | 1976-06-01 | — | — | US | disclosed |