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.
Predicted protein targets (top 17)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA1 | P00915 | 4/20 | 0.61 |
| ▸ | CA4 | P22748 | 2/20 | 0.44 |
| ▸ | MEN1 | O00255 | 1/20 | 0.43 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.43 |
| ▸ | CA5A | P35218 | 1/20 | 0.40 |
| ▸ | CA5B | Q9Y2D0 | 1/20 | 0.40 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.40 |
| ▸ | CA2 | P00918 | 2/20 | 0.36 |
| ▸ | LMNA | P02545 | 1/20 | 0.36 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.34 |
| ▸ | TSHR | P16473 | 2/20 | 0.33 |
| ▸ | THPO | P40225 | 1/20 | 0.33 |
| ▸ | FFAR3 | O14843 | 1/20 | 0.33 |
| ▸ | LCK | P06239 | 1/20 | 0.33 |
| ▸ | FYN | P06241 | 1/20 | 0.33 |
| ▸ | CES1 | P23141 | 1/20 | 0.32 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.31 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 SCHEMBL11660791 | 0.92 | CA1 (0.61) | CA1CA4MEN1KMT2ACA5A | |
| Acetic Acid SCHEMBL7211735 | 0.92 | — | — | |
| Acetic Acid SCHEMBL12465625 | 0.92 | CA1 (0.61) | CA1CA4MEN1KMT2ACA5A | |
| Acetic Acid SCHEMBL11660792 | 0.92 | CA1 (0.61) | CA1CA4MEN1KMT2ACA5A | |
| Acetic Acid SCHEMBL7517431 | 0.92 | — | — | |
| Acetic Acid SCHEMBL6403805 | 0.92 | CA1 (0.61) | CA1CA4MEN1KMT2ACA5A | |
| Acetic Acid SCHEMBL5499991 | 0.92 | CA1 (0.61) | CA1CA4MEN1KMT2ACA5A | |
| Acetic Acid SCHEMBL17312004 | 0.92 | CA1 (0.61) | CA1CA4MEN1KMT2ACA5A | |
| Acetic Acid SCHEMBL12484395 | 0.92 | — | — | |
| Acetic Acid SCHEMBL19432974 | 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 5 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114572941-B | Method for preparing copper chalcogenide heterojunction nano-material with excellent LSPR absorption intensity and spectral stability | 北京师范大学 | 2023-07-21 | — | — | CN | disclosed |
| US-6455742-B1 | LOW PRESSURE HYDROGENATION OF LACTIC ACID OR GLYCOLIC ACID TO ETHYLENE GLYCOL OR 1,2-PROPANEDIOL IN THE PRESENCE OF WATER, HYDROGEN AND COPPER SUPPORTED ON SILICA; CATALYSIS | WISCONSIN ALUMNI RESEARCH FOUNDATION | 2002-09-24 | — | — | US | disclosed |
| US-6441241-B1 | CONTACTING WITH A CATALYST COMPRISING ZERO VALENT COPPER IN THE PRESENCE OF HYDROGEN | WISCONSIN ALUMNI RESEARCH FOUNDATION | 2002-08-27 | — | — | US | disclosed |
| US-20020087035-A1 | Method for catalyticallly reducing carboxylic acid groups to hydroxyl groups in hydroxycarboxylic acids | WISCONSIN ALUMNI RESEARCH FOUNDATION. | 2002-07-04 | — | — | US | disclosed |
| WO-2001016063-A1 | METHOD FOR CATALYTICALLY REDUCING CARBOXYLIC ACID GROUPS TO HYDROXYL GROUPS IN HYDROXYCARBOXYLIC ACIDS | WISCONSIN ALUMNI RESEARCH FOUNDATION (US) | 2001-03-08 | — | — | WO | disclosed |