Known targets — ChEMBL curated mechanism
ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4
The experimentally established mechanism targets of Formic Acid. 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 | |
|---|---|---|---|---|
| Formic Acid SCHEMBL27719610 | 1.00 | — | — | |
| Formic Acid SCHEMBL7940435 | 0.94 | — | — | |
| Formic Acid SCHEMBL11329892 | 0.94 | — | — | |
| Formic Acid SCHEMBL8026877 | 0.94 | — | — | |
| Formic Acid SCHEMBL11558316 | 0.94 | — | — | |
| Formic Acid SCHEMBL8367150 | 0.94 | — | — | |
| Formic Acid SCHEMBL11329899 | 0.94 | — | — | |
| Formic Acid SCHEMBL11248324 | 0.93 | ALDH1A1 (0.38) | — | |
| Formic Acid SCHEMBL6682610 | 0.93 | ALDH1A1 (0.38) | — | |
| Formic Acid SCHEMBL6684167 | 0.93 | ALDH1A1 (0.38) | — |
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 580 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20230265342-A1 | QUANTUM DOT MATERIAL AND METHOD FOR PRODUCING QUANTUM DOT MATERIAL | SHOEI CHEMICAL, INC. (JP) | 2023-08-24 | — | — | US | claimed |
| US-11667838-B2 | Quantum dot material and method for producing quantum dot material | SHOEI CHEMICAL, INC. (JP) | 2023-06-06 | — | — | US | claimed |
| CN-109075222-B | Quantum dot material and method for producing quantum dot material | 昭荣化学工业株式会社 | 2021-09-24 | — | — | CN | claimed |
| CN-105980463-B | Optical article and production method comprising hard coat | 依视路国际公司 | 2019-09-10 | — | — | CN | claimed |
| US-20190112527-A1 | QUANTUM DOT MATERIAL AND METHOD FOR PRODUCING QUANTUM DOT MATERIAL | SHOEI CHEMICAL, INC. (JP) | 2019-04-18 | — | — | US | claimed |
| CN-109403028-A | A kind of method of modifying and modified heterocycle aramid fiber of heterocycle aramid fiber | 四川大学 | 2019-03-01 | — | — | CN | claimed |
| CN-105801364-B | A kind of preparation method of bromo hexitol | 广西梧州制药（集团）股份有限公司 | 2018-10-02 | — | — | CN | claimed |
| CN-105801371-B | Purposes of the oxidant in bromo-reaction | 广西梧州制药（集团）股份有限公司 | 2018-09-28 | — | — | CN | claimed |
| CN-105801374-B | A kind of synthetic method for improving bromo hexitol reaction product yield | 广西梧州制药（集团）股份有限公司 | 2018-05-15 | — | — | CN | claimed |
| WO-2016202894-A1 | METHOD OF CONVERTING ALCOHOL TO HALIDE | UNIVERSITAET DES SAARLANDES (DE) | 2016-12-22 | — | — | WO | claimed |
| EP-0282221-B1 | METHOD FOR RACEMIZATION OF OPTICALLY ACTIVE CHRYSANTHEMIC ACID OR ITS ESTER | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1992-01-15 | — | — | EP | claimed |
| US-4898655-A | Method for racemization of optically active chrysanthemic acid or its derivatives | SUMITOMO CHEMICAL COMPANY, LTD. (JP) | 1990-02-06 | — | — | US | claimed |
| US-4833250-A | Process of converting a carboxylic acid or carboxylic acid halide group to a trihalomethyl group | ICI AMERICAS INC. (US) | 1989-05-23 | — | — | US | claimed |
| US-4820864-A | Method for racemization of optically active chrysanthemic acid or its ester | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1989-04-11 | — | — | US | claimed |
| US-4812264-A | Method for racemization of optically active chrysanthemic acid derivatives | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1989-03-14 | — | — | US | claimed |
| EP-0299760-A1 | Method for racemization of optically active chrysanthemic acid or its derivatives | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1989-01-18 | — | — | EP | claimed |
| EP-0289324-A1 | Method for racemization of optically active chrysanthemic acid derivatives | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1988-11-02 | — | — | EP | claimed |
| EP-0282221-A2 | Method for racemization of optically active chrysanthemic acid or its ester | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1988-09-14 | — | — | EP | claimed |
| EP-0281965-A1 | Method of converting a carboxylic acid or carboxylic acid halide group to a trihalomethyl group | ICI AMERICAS INC. (US) | 1988-09-14 | — | — | EP | claimed |
| EP-0169144-A2 | Process for the preparation of 7-amino and 7-substituted amino-desacetoxycephalosporins from the corresponding 6-substituted amino penicillin sulphoxides | GEMA S.A. (ES) | 1986-01-22 | — | — | EP | claimed |