Known targets — ChEMBL curated mechanism
ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of None. 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 | |
|---|---|---|---|---|
| SCHEMBL6449559 | 0.89 | TSHR (0.33) | — | |
| SCHEMBL105342 | 0.89 | — | — | |
| SCHEMBL15643453 | 0.89 | — | — | |
| SCHEMBL3658482 | 0.89 | TSHR (0.33) | — | |
| SCHEMBL6943728 | 0.89 | TSHR (0.33) | — | |
| SCHEMBL3458910 | 0.89 | — | — | |
| SCHEMBL6449456 | 0.89 | TSHR (0.33) | — | |
| SCHEMBL6449280 | 0.89 | TSHR (0.33) | — | |
| SCHEMBL8916717 | 0.89 | TSHR (0.33) | — | |
| SCHEMBL6448290 | 0.89 | TSHR (0.33) | — |
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
Appears in 4071 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122071421-A | Process for efficiently preparing acrylamide monomer by low-cost base catalytic pyrolysis | 深圳有为技术控股集团有限公司 | 2026-05-22 | — | — | CN | claimed |
| CN-116854630-B | Methods and intermediates for preparing therapeutic compounds useful in the treatment of retroviral infections | 吉利德科学公司 | 2026-05-19 | — | — | CN | claimed |
| CN-122035819-A | Sodium-rich hard carbon material, preparation method thereof and sodium ion battery | 广东海四达钠星技术有限公司 | 2026-05-15 | — | — | CN | claimed |
| CN-122037028-A | Liquid polybutadiene rubber with wide molecular weight distribution and preparation method thereof | 中国科学院长春应用化学研究所 | 2026-05-15 | — | — | CN | claimed |
| EP-4037809-B1 | ELEMENTAL SULFUR ANALYSIS IN FLUIDS | CONOCOPHILLIPS CO (US) | 2026-05-06 | — | — | EP | claimed |
| US-12612369-B1 | Eco-friendly synthesis of a novel nicotinonitrile derivative (MNPN) with antibacterial and anti-inflammatory activities for preventing pressure ulcers in individuals with disabilities | King Faisal University (SA) | 2026-04-28 | — | — | US | claimed |
| EP-4353774-B1 | LOW-TEMPERATURE ORGANOCATALYZED DEPOLYMERIZATION OF POLY(ETHYLENE TEREPHTHALATE) | POLYKEY POLYMERS S L (ES) | 2025-09-10 | — | — | EP | claimed |
| CN-120199805-A | Preparation method of self-supplementing sodium P2 type positive electrode material | 中国科学院化学研究所 | 2025-06-24 | — | — | CN | claimed |
| EP-3702384-B1 | MICROSPHERIC IONOMER HAVING CROSS-LINKING STRUCTURE, PREPARATION METHOD THEREFOR, APPLICATIONS THEREOF, AND PREPARATION SYSTEM THEREOF | CHINA PETROLEUM & CHEM CORP (CN) | 2025-05-14 | — | — | EP | claimed |
| CN-119954866-A | Pentafluoroalkoxy ring preparation method of triphosphazene | 安徽金禾合成材料研究院有限公司 | 2025-05-09 | — | — | CN | claimed |
| EP-0343812-A1 | Process for preparing trans-2,2-dimethyl-3-(2,2-dihalovinyl)-cyclopropane carboxylic acid esters | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1989-11-29 | — | — | EP | claimed |
| US-4868345-A | METAL HYDRIDE, ALCOHOL OR ALCOHOLATE, GROUP 8 COMPOUND | SHELL OIL COMPANY (US) | 1989-09-19 | — | — | US | claimed |
| EP-0322989-A2 | Process for the production of methanol | SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) | 1989-07-05 | — | — | EP | claimed |
| EP-0308030-A1 | Process for hydrogenation of esters into alcohols | SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) | 1989-03-22 | — | — | EP | claimed |
| EP-0297783-A2 | A method of producing 4-alkoxypyridine-1-oxides | Takeda Chemical Industries, Ltd. (JP) | 1989-01-04 | — | — | EP | claimed |
| EP-0269109-A2 | Process for the preparation of dialkyl 2-vinylcyclopropane-1,1-dicarboxylates | HENKEL CORPORATION (US) | 1988-06-01 | — | — | EP | claimed |
| EP-0052339-A1 | Fluorobarbituric acid derivatives and their preparation | Daikin Kogyo Co., Ltd. (JP) | 1982-05-26 | — | — | EP | claimed |
| US-3985834-A | Phosphazene composition | ETHYL CORPORATION (US) | 1976-10-12 | — | — | US | claimed |
| US-3966749-A | Novel synthesis of optically active m-acyloxy-α-[(methylamino)methyl]benzyl alcohols, the pharmaceutically acceptable acid addition salts thereof and intermediate useful in the preparation thereof | INTERX RESEARCH CORPORATION (US) | 1976-06-29 | — | — | US | claimed |
| US-3965219-A | Continuous process for the esterification of phosphonitrilic chloride polymers | FMC CORPORATION (US) | 1976-06-22 | — | — | US | claimed |