Acetic Acid

Acetic Acid

SCHEMBL9549682

CC(=O)O.CC(=O)OCCNC(C)(C)C.c1ccc(P(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.43

Full drug profile on Sugi Atlas →

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 20)

geneUniProtsupporting neighboursconfidence
ADRB2 known ✓ P07550 2/20 0.39
SCN5A known ✓ Q14524 1/20 0.36
GAA P10253 2/20 0.43
ALDH1A1 P00352 4/20 0.41
KDM4E B2RXH2 6/20 0.39
RECQL P46063 1/20 0.39
ADRB1 P08588 2/20 0.39
ADRB3 P13945 2/20 0.39
POLB P06746 1/20 0.38
MEN1 O00255 2/20 0.37
KMT2A Q03164 2/20 0.37
CYP1A2 P05177 1/20 0.37
CYP3A4 P08684 1/20 0.37
MAPK1 P28482 1/20 0.36
HTT P42858 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
HSD17B10 Q99714 1/20 0.36
HTR1A P08908 1/20 0.36
CYP2D6 P10635 1/20 0.36
SCN1A P35498 1/20 0.36

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
SCHEMBL14608698 0.79 ALDH1A1 (0.43) GAAALDH1A1KDM4EPOLBMEN1
SCHEMBL9549641 0.77 GAA (0.40) GAAALDH1A1KDM4EADRB2ADRB1
Ethyl Acetate SCHEMBL9063181 0.75 ALDH1A1 (0.52) GAAALDH1A1RECQLMEN1KMT2A
Acetic Acid SCHEMBL9549765 0.75 RAD52 (0.50) ALDH1A1KDM4ESMN1; SMN2
SCHEMBL21606341 0.74 GAA (0.40) GAAALDH1A1KDM4EADRB2ADRB1
SCHEMBL4388901 0.73 ALDH1A1 (0.50) ALDH1A1KDM4ECYP1A2CYP3A4SMN1; SMN2
Ethyl Acetate SCHEMBL811125 0.73 ALDH1A1 (0.54) GAAALDH1A1RECQLMEN1KMT2A
Acetic Acid SCHEMBL9549696 0.72 RAD52 (0.55) GAAALDH1A1KDM4EMAPK1SMN1; SMN2
Acetic Acid Methyl Ester SCHEMBL19208995 0.72 TDP1 (0.55) GAAALDH1A1KDM4EKMT2ACYP3A4
Acetic Acid SCHEMBL7629010 0.72 CYP3A4 (0.67) GAAALDH1A1KDM4EPOLBCYP3A4

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