Acetic Acid

Acetic Acid

SCHEMBL9549696

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

nearest known ligand 0.57

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 15)

geneUniProtsupporting neighboursconfidence
RAD52 P43351 1/20 0.55
GAA P10253 1/20 0.44
KDM4E B2RXH2 6/20 0.44
ALDH1A1 P00352 5/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
CHRM2 P08172 1/20 0.43
CHRM4 P08173 1/20 0.43
CHRM1 P11229 1/20 0.43
CHRM3 P20309 1/20 0.43
MAPK1 P28482 1/20 0.43
HSD17B10 Q99714 1/20 0.43
LSS P48449 1/20 0.42
TSHR P16473 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
MAPT P10636 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
Acetic Acid SCHEMBL9549688 0.96 RAD52 (0.53) RAD52GAAKDM4EALDH1A1SMN1; SMN2
Acetic Acid SCHEMBL9549765 0.91 RAD52 (0.50) RAD52KDM4EALDH1A1SMN1; SMN2CHRM2
SCHEMBL9549624 0.85 KDM4E (0.47) RAD52GAAKDM4EALDH1A1SMN1; SMN2
Acetic Acid SCHEMBL9549719 0.82 CHRM2 (0.48) GAAALDH1A1SMN1; SMN2CHRM2CHRM4
Acetic Acid SCHEMBL9549791 0.81 ALDH1A1 (0.44) RAD52GAAKDM4EALDH1A1SMN1; SMN2
SCHEMBL26314 0.79 ALDH1A1 (0.56) RAD52GAAKDM4EALDH1A1SMN1; SMN2
Acetic Acid SCHEMBL9549665 0.78 CHRM1 (0.53) RAD52KDM4EALDH1A1SMN1; SMN2CHRM2
Water SCHEMBL28087308 0.77 ALDH1A1 (0.54) RAD52GAAKDM4EALDH1A1SMN1; SMN2
Ammonia Solution, Strong SCHEMBL7710348 0.77 ALDH1A1 (0.54) RAD52GAAKDM4EALDH1A1SMN1; SMN2
Ethyl Acetate SCHEMBL9063181 0.76 ALDH1A1 (0.52) GAAALDH1A1HSD17B10TSHRMAPT

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