Acetic Acid

Acetic Acid

SCHEMBL9549681

CC(=O)[O-].CC(=O)[O-].CN(CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)Cc1ccccc1.CN(CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)Cc1ccccc1

nearest known ligand 0.48

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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)

geneUniProtsupporting neighboursconfidence
▸ CARM1 Q86X55 1/20 0.46
▸ PRMT6 Q96LA8 1/20 0.46
▸ PRMT8 Q9NR22 1/20 0.46
▸ SMN1; SMN2 Q16637 1/20 0.46
▸ SIGMAR1 Q99720 4/20 0.44
▸ TMEM97 Q5BJF2 3/20 0.44
▸ ALDH1A1 P00352 2/20 0.44
▸ CYP1A2 P05177 1/20 0.44
▸ CYP2D6 P10635 1/20 0.44
▸ TSHR P16473 1/20 0.44
▸ CYP2C19 P33261 1/20 0.44
▸ KDM4A O75164 1/20 0.42
▸ KDM4C Q9H3R0 1/20 0.42
▸ NPC1 O15118 2/20 0.41
▸ RAB9A P51151 2/20 0.41
▸ CA12 O43570 1/20 0.41
▸ CA9 Q16790 1/20 0.41

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.

Compoundsimilaritytop predictedshared targets
Hydrochloric Acid SCHEMBL9549758 0.88 CARM1 (0.55) CARM1PRMT6PRMT8SMN1; SMN2SIGMAR1
Bromide SCHEMBL9549584 0.88 CARM1 (0.55) CARM1PRMT6PRMT8SMN1; SMN2SIGMAR1
Phosphoric Acid SCHEMBL9549658 0.87 SIGMAR1 (0.47) CARM1PRMT6PRMT8SIGMAR1TMEM97
Acetic Acid SCHEMBL9549770 0.83 TSHR (0.50) ALDH1A1CYP1A2CYP2D6TSHRCYP2C19
Acetic Acid SCHEMBL9848332 0.81 TSHR (0.49) ALDH1A1CYP1A2CYP2D6TSHRCYP2C19
Acetic Acid SCHEMBL9549690 0.79 ALDH1A1 (0.46) ALDH1A1CYP1A2CYP2D6TSHRCYP2C19
Bicarbonate SCHEMBL8973196 0.78 TSHR (0.52) ALDH1A1CYP1A2CYP2D6TSHRCYP2C19
Acetic Acid SCHEMBL9549671 0.77 TSHR (0.47) SMN1; SMN2SIGMAR1TMEM97ALDH1A1CYP1A2
Acetic Acid SCHEMBL9549706 0.77 HTR2A (0.50) SMN1; SMN2SIGMAR1ALDH1A1CYP1A2CYP2D6
Oxalic Acid SCHEMBL9549804 0.76 TSHR (0.50) ALDH1A1CYP1A2CYP2D6TSHRCYP2C19

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5208317-A Molding materials of cured epoxy resins THE DOW CHEMICAL COMPANY (US) 1993-05-04 — — US disclosed
US-5109099-A ADVANCING EPOXY RESINS IN PRESENCE OF AMINO GROUP-CONTAINING PHOSPHONIUM CATALYST THE DOW CHEMICAL COMPANY (US) 1992-04-28 — — US disclosed
EP-0441243-A2 Precatalyzed catalyst compositions, process for preparing epoxy resins, curable compositions, articles resulting from curing the resultant compositions THE DOW CHEMICAL COMPANY (US) 1991-08-14 — — EP disclosed
US-4981926-A Rapid and selective curing using phosphonium catalyst containing an amine group; polyepoxides THE DOW CHEMICAL COMPANY (US) 1991-01-01 — — US disclosed
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