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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL27864795 | 0.93 | — | — | |
| SCHEMBL11677710 | 0.92 | — | — | |
| SCHEMBL4068319 | 0.92 | — | — | |
| Potassium Ion SCHEMBL7861827 | 0.92 | — | — | |
| SCHEMBL11679695 | 0.92 | — | — | |
| SCHEMBL9583828 | 0.92 | — | — | |
| SCHEMBL4074588 | 0.92 | — | — | |
| SCHEMBL4823906 | 0.92 | — | — | |
| SCHEMBL7854946 | 0.92 | — | — | |
| SCHEMBL11677345 | 0.92 | — | — |
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 76 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-101222069-A | Sealing maintenance-free lead acid accumulator for mining safety helmet lamp | TIANJIN GUANYUAN TECHNOLOGY DE (CN) | 2008-07-16 | — | — | CN | claimed |
| CN-1933231-A | High energy full sealed non-maintenance lead-acid battery for miner's safety cap-lamp | SUZHONG BATTERY SCIENCE & TECH (CN) | 2007-03-21 | — | — | CN | claimed |
| CN-1652388-A | High-energy sealed maintenance-free lead-acid ccumulator for mine lamp | CHEN YOUXIAO (CN) | 2005-08-10 | — | — | CN | claimed |
| EP-0900227-B1 | IMPROVED PROCESS FOR THE SYNTHESIS OF DIESTERS OF PHOSPHORIC ACID 2,5-DIOXO-4,4-DIPHENYL-IMIDAZOLIDIN-1-YLMETHYL ESTER | WARNER LAMBERT CO (US) | 2001-12-12 | — | — | EP | claimed |
| US-6022975-A | Process for the synthesis of diesters of phosphoric acid 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl ester | WARNER-LAMBERT COMPANY (US) | 2000-02-08 | — | — | US | claimed |
| EP-0900227-A1 | IMPROVED PROCESS FOR THE SYNTHESIS OF DIESTERS OF PHOSPHORIC ACID 2,5-DIOXO-4,4-DIPHENYL-IMIDAZOLIDIN-1-YLMETHYL ESTER | WARNER-LAMBERT COMPANY (US) | 1999-03-10 | — | — | EP | claimed |
| WO-1997041132-A1 | IMPROVED PROCESS FOR THE SYNTHESIS OF DIESTERS OF PHOSPHORIC ACID 2,5-DIOXO-4,4-DIPHENYL-IMIDAZOLIDIN-1-YLMETHYL ESTER | WARNER-LAMBERT COMPANY (US) | 1997-11-06 | — | — | WO | claimed |
| EP-0519953-A1 | ACYL PHOSPHATE ESTERS AND MODIFICATION OF PROTEINS THEREWITH. | UNIV TORONTO (CA) | 1992-12-30 | — | — | EP | claimed |
| WO-1991013891-A1 | ACYL PHOSPHATE ESTERS AND MODIFICATION OF PROTEINS THEREWITH | THE UNIVERSITY OF TORONTO INNOVATIONS FOUNDATION (CA) | 1991-09-19 | — | — | WO | claimed |
| US-20260125405-A1 | METHOD FOR PRODUCING IMIDIC ACID OR IMIDIC ACID SALT | CENTRAL GLASS COMPANY, LIMITED (JP) | 2026-05-07 | — | — | US | disclosed |
| EP-4585559-A1 | METHOD FOR PRODUCING IMIDIC ACID OR IMIDIC ACID SALT | Central Glass Company, Limited (JP) | 2025-07-16 | — | — | EP | disclosed |
| CN-119998229-A | Method for producing imide acid or imide acid salt | 中央硝子株式会社 | 2025-05-13 | — | — | CN | disclosed |
| WO-2025095088-A1 | NON-AQUEOUS ELECTROLYTE SOLUTION FOR SECONDARY BATTERY, AND SECONDARY BATTERY PROVIDED WITH SAID SOLUTION | ステラケミファ株式会社 | 2025-05-08 | — | — | WO | disclosed |
| WO-2025075065-A1 | THERMALLY CATIONICALLY POLYMERIZABLE COMPOSITION, USE OF SAME, CATIONIC POLYMERIZATION METHOD USING SAME, AND STABILIZER FOR THERMALLY CATIONICALLY POLYMERIZABLE COMPOSITIONS | 三新化学工業株式会社 | 2025-04-10 | — | — | WO | disclosed |
| WO-1991013891-A1 | ACYL PHOSPHATE ESTERS AND MODIFICATION OF PROTEINS THEREWITH | THE UNIVERSITY OF TORONTO INNOVATIONS FOUNDATION (CA) | 1991-09-19 | — | — | WO | disclosed |
| US-4900782-A | Stabilized polyelectrolyte precursors of poly(aromatic and heteroaromatic vinylenes) | ALLIED-SIGNAL INC. (US) | 1990-02-13 | — | — | US | disclosed |
| EP-0127581-B1 | MICROORGANISMS OF THE GENUS PSEUDOMONAS AND METHOD FOR THE DECOMPOSITION OF COMPOUNDS CONTAINING METHYL GROUPS IN AQUEOUS SOLUTIONS | CIBA-GEIGY AG (CH) | 1989-05-10 | — | — | EP | disclosed |
| EP-0187732-A2 | Microorganisms of the genus Hyphomicrobium and process for the decomposition, in an aqueous medium, of compounds which contain methyl groups, especially phosphorous compounds which contain methyl groups | CIBA-GEIGY AG (CH) | 1986-07-16 | — | — | EP | disclosed |
| EP-0127581-A1 | Microorganisms of the genus Pseudomonas and method for the decomposition of compounds containing methyl groups in aqueous solutions | CIBA-GEIGY AG (CH) | 1984-12-05 | — | — | EP | disclosed |
| US-4020101-A | CLEANSING COMPOUNDS | BAYER AKTIENGESELLSCHAFT (DT) | 1977-04-26 | — | — | US | disclosed |