Known targets — ChEMBL curated mechanism
ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Acetic 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 | |
|---|---|---|---|---|
| Acetic Acid SCHEMBL5867869 | 1.00 | FFAR3 (0.88) | — | |
| Acetic Acid SCHEMBL234816 | 1.00 | FFAR3 (0.88) | — | |
| Acetic Acid SCHEMBL11858088 | 1.00 | FFAR3 (0.88) | — | |
| Acetic Acid SCHEMBL536985 | 1.00 | — | — | |
| Acetic Acid SCHEMBL11857925 | 1.00 | FFAR3 (0.88) | — | |
| Acetic Acid SCHEMBL226015 | 1.00 | — | — | |
| Acetic Acid SCHEMBL52435 | 1.00 | — | — | |
| Acetic Acid SCHEMBL51762 | 1.00 | — | — | |
| Acetic Acid SCHEMBL5573359 | 1.00 | FFAR3 (0.88) | — | |
| Acetic Acid SCHEMBL11776704 | 1.00 | FFAR3 (0.88) | — |
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 27 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114496333-A | Based on63Heterojunction high-efficiency nuclear battery with NiO carrier transmission layer and preparation method | 吉林大学 | 2022-05-13 | — | — | CN | claimed |
| CN-114496333-A | Based on63Heterojunction high-efficiency nuclear battery with NiO carrier transmission layer and preparation method | 吉林大学 | 2022-05-13 | — | — | CN | disclosed |
| CN-110455979-B | High-selectivity sensitive material for monitoring trace ethanol in air | 北京联合大学 | 2021-06-08 | — | — | CN | disclosed |
| CN-108864625-B | Transparent heat-insulating anti-ultraviolet nano composite sheet and preparation method thereof | 宁波海奇合昇环能科技有限公司 | 2021-05-11 | — | — | CN | disclosed |
| CN-108724856-B | Laminated glass, hollow glass comprising laminated glass and manufacturing method of hollow glass | 宁波海奇合昇环能科技有限公司 | 2021-02-02 | — | — | CN | disclosed |
| CN-108727635-B | Core-shell structure bifunctional nanoparticle liquid-phase transparent dispersion and preparation method thereof | 宁波海奇合昇环能科技有限公司 | 2020-07-17 | — | — | CN | disclosed |
| CN-110672591-A | Low-temperature response sensitive material for formaldehyde and trimethylamine in air | 北京联合大学 | 2020-01-10 | — | — | CN | disclosed |
| CN-101511907-B | Polyester resin composition, process for production thereof, and laminated polyester film | TORAY INDUSTRIES | 2012-07-04 | — | — | CN | disclosed |
| CN-101511907-A | Polyester resin composition, process for production thereof, and laminated polyester film | TORAY INDUSTRIES (JP) | 2009-08-19 | — | — | CN | disclosed |
| US-20090105633-A1 | ULTRASOUND ASSEMBLY FOR USE WITH LIGHT ACTIVATED DRUGS | TACHIBANA KATSURO | 2009-04-23 | — | — | US | disclosed |
| US-5807664-A | TABULAR SILVER CHLORIDE GRAINS | KONICA CORPORATION (JP) | 1998-09-15 | — | — | US | disclosed |
| US-5667960-A | VINYL SULFONE DERIVATIVES | KONICA CORPORATION (JP) | 1997-09-16 | — | — | US | disclosed |
| EP-0782579-A1 | DNA PHOTOCLEAVAGE USING TEXAPHYRINS | THE BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 1997-07-09 | — | — | EP | disclosed |
| US-5607924-A | COVALENTLY COUPLED TO A SITE-DIRECTING MOLECULE PRFERABLY OLEGONUCLEOTIDE; EXPOSURE TO LIGHT | PHARMACYCLICS, INC. (US) | 1997-03-04 | — | — | US | disclosed |
| US-5567687-A | USEFUL IN PHOTODYNAMIC THERAPY AND LIGHT-INDUCED CLEAVAGE OF A POLYMER OF DEOXYRIBONUCLEIC ACID | UNIVERSITY OF TEXAS (US) | 1996-10-22 | — | — | US | disclosed |
| US-5559207-A | PORPHYRIN DERIVATIVES COMPLEXED WITH LANTHANIDE METALS, HYDROLYSIS OF RNA PHOSPHATE ESTERS, MEDICAL TREATMENTS AND THERAPIES DEPENDENT ON SUCH HYDROLYSIS | BOARD OF REGENTS, UNIVERSITY OF TEXAS (US) | 1996-09-24 | — | — | US | disclosed |
| WO-1996009315-A1 | DNA PHOTOCLEAVAGE USING TEXAPHYRINS | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 1996-03-28 | — | — | WO | disclosed |
| EP-0702685-A1 | TEXAPHYRIN METAL COMPLEX MEDIATED ESTER HYDROLYSIS | THE BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 1996-03-27 | — | — | EP | disclosed |
| WO-1994029316-A2 | TEXAPHYRIN METAL COMPLEX MEDIATED ESTER HYDROLYSIS | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 1994-12-22 | — | — | WO | disclosed |
| US-4211769-A | PEPTIDE HAVING LUTEINIZING HORMONE RELEASING HORMONE ACTIVITY, POLYBASIC CARBOXYLIC ACID | TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) | 1980-07-08 | — | — | US | disclosed |