Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Hydrochloric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL28318965 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL601240 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL18971 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL11740435 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL25364759 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL10897118 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL11155184 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL29089392 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL9749716 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL20560712 | 0.82 | — | — |
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 247 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116635392-A | Substituted azabicyclooctane compounds, intermediates thereof and methods of making | 上海海雁医药科技有限公司 | 2023-08-22 | — | — | CN | claimed |
| CN-112480107-B | Substituted azabicyclooctane compounds, intermediates therefor and processes for their preparation | 上海海雁医药科技有限公司 | 2022-08-16 | — | — | CN | claimed |
| WO-2022111683-A1 | SUBSTITUTED AZABICYCLOOCTANE COMPOUND AND PREPARATION METHOD THEREFOR, AND INTERMEDIATE AND PREPARATION METHOD THEREFOR | 上海海雁医药科技有限公司 | 2022-06-02 | — | — | WO | claimed |
| CN-112480107-A | Substituted azabicyclooctane compounds, intermediates therefor and processes for their preparation | 上海海雁医药科技有限公司 | 2021-03-12 | — | — | CN | claimed |
| CN-105498824-B | Hydrocarbons reforming catalyst of containing mesopore molecular sieve and preparation method thereof | 中国石油化工股份有限公司 | 2018-06-19 | — | — | CN | claimed |
| CN-105498824-A | Hydrocarbon reforming catalyst containing mesoporous molecular sieve, and preparation method thereof | CHINA PETROLEUM & CHEM CORP | 2016-04-20 | — | — | CN | claimed |
| CN-100372442-C | Organic electroluminescent devices | KIDO JUNJI (JP) | 2008-02-27 | — | — | CN | claimed |
| US-6139628-A | Method of forming gallium nitride crystal | MATSUSHITA ELECTRONICS CORPORATION (JP) | 2000-10-31 | — | — | US | claimed |
| CN-1236289-A | Organic electroluminescent devices | JUNJI KIDO (JP) | 1999-11-24 | — | — | CN | claimed |
| US-3989882-A | Process for preparing an alternating copolymer of a conjugated vinyl compound and an olefinic unsaturated compound | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1976-11-02 | — | — | US | claimed |
| US-12234312-B2 | Solid catalyst component for olefin polymerization | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2025-02-25 | — | — | US | disclosed |
| CN-119161509-A | Solid catalyst component for olefin polymerization | 住友化学株式会社 | 2024-12-20 | — | — | CN | disclosed |
| US-12157956-B2 | Optimized heteroepitaxial growth of semiconductors | UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE AIR FORCE (US) | 2024-12-03 | — | — | US | disclosed |
| US-12116695-B2 | Optimized heteroepitaxial growth of semiconductors | UNITED STATES OF AMERICA AS REPRESENTED BY SECRETARY OF THE AIR FORCE (US) | 2024-10-15 | — | — | US | disclosed |
| CN-114057913-B | Solid catalyst component for olefin polymerization | 住友化学株式会社 | 2024-10-11 | — | — | CN | disclosed |
| WO-1981001289-A1 | CATALYSED ALTERNATING COPOLYMERISATION AND PRODUCT | BAMFORD C | 1981-05-14 | — | — | WO | disclosed |
| US-4120808-A | Gas discharge dielectric containing a source of boron, gallium, indium, or thallium | OWENS-ILLINOIS, INC. (US) | 1978-10-17 | — | — | US | disclosed |
| US-4121032-A | Process for preparing alternating copolymer of conjugated vinyl compound and olefinic unsaturated compound with oxygen and boron compound | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1978-10-17 | — | — | US | disclosed |
| US-4028578-A | Gas discharge dielectric containing a source of boron, gallium, indium, or thallium | OWENS-ILLINOIS, INC. (US) | 1977-06-07 | — | — | US | disclosed |
| US-3989882-A | Process for preparing an alternating copolymer of a conjugated vinyl compound and an olefinic unsaturated compound | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1976-11-02 | — | — | US | disclosed |