⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL27657786 | 0.97 | GAA (0.63) | — | |
| SCHEMBL5075 | 0.97 | — | — | |
| Alcohol SCHEMBL10983490 | 0.94 | GAA (0.60) | — | |
| Methane SCHEMBL28593248 | 0.94 | GAA (0.60) | — | |
| SCHEMBL28265902 | 0.94 | — | — | |
| SCHEMBL2052937 | 0.94 | — | — | |
| Potassium SCHEMBL31180265 | 0.94 | — | — | |
| SCHEMBL10989272 | 0.94 | — | — | |
| Ammonia Solution, Strong SCHEMBL16879889 | 0.94 | — | — | |
| SCHEMBL28236344 | 0.94 | — | — |
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 16 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| JP-11225590-A | — | — | None | — | — | JP | disclosed |
| CN-115232772-A | Method for producing caproic acid by using RF1 bacteria and combined clostridium keshiii | 湖北稻花香酒业股份有限公司 | 2022-10-25 | — | — | CN | disclosed |
| CN-109956958-A | A kind of 7- amino -3- methoxy -3- cephem -4- carboxylic acid synthetic method | 河北合佳医药科技集团股份有限公司 | 2019-07-02 | — | — | CN | disclosed |
| CN-106674135-B | A method of synthesis uracil | 新乡制药股份有限公司 | 2019-03-15 | — | — | CN | disclosed |
| CN-106674135-A | Uracil synthesizing method | 新乡制药股份有限公司 | 2017-05-17 | — | — | CN | disclosed |
| CN-102633908-A | Method for preparing high-quality LMW (low molecular weight) heparins | XIAOGANG LEI | 2012-08-15 | — | — | CN | disclosed |
| US-7091225-B2 | Substituted oxazoles and thiazoles as hPPAR alpha agonists | SMITHKLINE BEECHAM CORPORATION (US) | 2006-08-15 | — | — | US | disclosed |
| US-20040147571-A1 | Substituted oxazoles and thiazoles as hppar alpha agonists | SMITHKLINE BEECHAM CORPORATION | 2004-07-29 | — | — | US | disclosed |
| EP-1345916-A1 | SUBSTITUTED OXAZOLES AND THIAZOLES AS HPPAR ALPHA AGONISTS | GLAXO GROUP LIMITED (GB) | 2003-09-24 | — | — | EP | disclosed |
| WO-2002050047-A1 | SUBSTITUED OXAZOLES AND THIAZOLES AS HPPAR ALPHA AGONISTS | GLAXO GROUP LIMITED (GB) | 2002-06-27 | — | — | WO | disclosed |
| JP-H11225590-A | COATING FOR PLANT AND FORMATION OR REMOVAL OF COATING FOR PLANT | COLOR CHEMICAL KOGYO KK | 1999-08-24 | — | — | JP | disclosed |
| EP-0177098-B1 | SURFACTANT COMPOSITION AND PROCESS FOR THE PRODUCTION OF OIL USING SUCH A COMPOSITION | SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) | 1989-12-27 | — | — | EP | disclosed |
| EP-0177098-A2 | Surfactant composition and process for the production of oil using such a composition | SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) | 1986-04-09 | — | — | EP | disclosed |
| US-4228300-A | Polycarboxylate ethers | MONSANTO COMPANY (US) | 1980-10-14 | — | — | US | disclosed |
| US-4156785-A | FROM AN UNSATURATED HALOGEN COMPOUND, CARBON MONOXIDE AND AN ALKALI METAL ALCOHOLATE USING NICKEL OR COBALT CARBONYL AS CATALYST | DYNAMIT NOBEL AKTIENGESELLSCHAFT (DE) | 1979-05-29 | — | — | US | disclosed |
| US-4057388-A | Dry heat process for dyeing and printing organic material which can be dyed with cationic dyestuffs | CIBA-GEIGY AG (CH) | 1977-11-08 | — | — | US | disclosed |