Acetic Acid

Acetic Acid

SCHEMBL7199841

CC(=O)O.CC(=O)[O-].COc1cccc(C[P+](c2cccc(C)c2)(c2cccc(C)c2)c2cccc(C)c2)c1

nearest known ligand 0.46

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 14)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.44
ACHE P22303 1/20 0.44
MAOB P27338 1/20 0.44
TAAR1 Q96RJ0 2/20 0.43
CTBP2 P56545 1/20 0.43
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
HSD17B2 P37059 1/20 0.43
MTNR1A P48039 2/20 0.43
MTNR1B P49286 2/20 0.43
ALDH1A1 P00352 1/20 0.40
HTT P42858 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
GAA P10253 1/20 0.40

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 SCHEMBL8750057 0.97 ACHE (0.46) CYP1A2ACHEMAOBTAAR1CTBP2
Acetic Acid SCHEMBL7197934 0.90 L3MBTL1 (0.46) CYP1A2MAOBTAAR1CTBP2MEN1
Acetic Acid SCHEMBL7200644 0.90 NPC1 (0.44) MEN1KMT2AALDH1A1HTTSMN1; SMN2
Succinic Acid SCHEMBL7199837 0.90 HSD17B2 (0.46) CYP1A2ACHEMAOBTAAR1CTBP2
Acetic Acid SCHEMBL8750051 0.87 L3MBTL1 (0.47) CYP1A2MAOBTAAR1CTBP2MEN1
Acetic Acid SCHEMBL8750094 0.87 NPC1 (0.46) MEN1KMT2AALDH1A1HTTSMN1; SMN2
Acetic Acid SCHEMBL7193257 0.87 SNCA (0.41) CYP1A2CTBP2MEN1KMT2AALDH1A1
Bromide SCHEMBL7200811 0.87 ACHE (0.55) ACHEMAOBTAAR1HSD17B2
Hydrochloric Acid SCHEMBL7195803 0.87 ACHE (0.55) ACHEMAOBTAAR1HSD17B2
Iodide SCHEMBL7201355 0.87 ACHE (0.55) ACHEMAOBTAAR1HSD17B2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0624173-B2 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 2003-04-09 EP disclosed
EP-0624173-B1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 1997-04-02 EP disclosed
EP-0624173-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS. DOW CHEMICAL CO (US) 1994-11-17 EP disclosed
US-5360886-A Alklyphenylphosphine or phosphonium catalyst THE DOW CHEMICAL COMPANY (US) 1994-11-01 US disclosed
US-5310853-A Epoxy resins THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
WO-1993015126-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS THE DOW CHEMICAL COMPANY (US) 1993-08-05 WO disclosed
US-5202407-A Phosphonium or phosphine catalyst having at least three alkylphenyl groups attached to phosphorus atom THE DOW CHEMICAL COMPANY (US) 1993-04-13 US disclosed