Acetic Acid

Acetic Acid

SCHEMBL1033263

CC(=O)[O-].Cc1ccc([P+](c2ccc(C)cc2)(c2ccc(C)cc2)c2ccc(C)cc2)cc1

nearest known ligand 0.42

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
ALDH1A1 P00352 5/20 0.42
LMNA P02545 3/20 0.42
CES2 O00748 2/20 0.42
CES1 P23141 2/20 0.42
TDP1 Q9NUW8 4/20 0.41
SMN1; SMN2 Q16637 3/20 0.41
ACHE P22303 2/20 0.39
HSD17B10 Q99714 1/20 0.39
CA1 P00915 1/20 0.38
PKM P14618 3/20 0.38
HTT P42858 2/20 0.38
ATM Q13315 2/20 0.38
NPSR1 Q6W5P4 2/20 0.38
GAA P10253 2/20 0.38
HPGD P15428 1/20 0.38
NLRP1 Q9C000 1/20 0.38
MEN1 O00255 1/20 0.38
NTSR1 P30989 1/20 0.38
KMT2A Q03164 1/20 0.38
NPC1 O15118 1/20 0.38

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 SCHEMBL7060294 0.92 CES2 (0.45) ALDH1A1LMNACES2CES1SMN1; SMN2
4-Methylbenzoic Acid SCHEMBL11575392 0.85 ALDH1A1 (0.48) ALDH1A1LMNACES2CES1TDP1
Acetic Acid SCHEMBL9068172 0.84 MAPT (0.42) ALDH1A1LMNACES2CES1TDP1
SCHEMBL7874663 0.82 ACHE (0.50) ALDH1A1LMNATDP1ACHEHSD17B10
Benzoic Acid SCHEMBL7872905 0.80 CA2 (0.57) ALDH1A1LMNACES2CES1TDP1
Acetic Acid SCHEMBL7606374 0.80 DNM1 (0.41) ALDH1A1LMNATDP1CA1HTT
Bromide SCHEMBL2494995 0.79 ACHE (0.53) ALDH1A1LMNACES2CES1TDP1
Water SCHEMBL4384420 0.79 ACHE (0.53) ALDH1A1LMNACES2CES1TDP1
Iodide SCHEMBL10656368 0.79 ACHE (0.53) ALDH1A1LMNACES2CES1TDP1
Hydrochloric Acid SCHEMBL7932457 0.79 ACHE (0.53) ALDH1A1LMNACES2CES1TDP1

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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7122613-B1 Method for the production of polycarbonates GENERAL ELECTRIC COMPANY (US) 2006-10-17 US claimed
EP-1578840-A1 METHOD FOR THE PRODUCTION OF POLYCARBONATES General Electric Company (US) 2005-09-28 EP claimed
WO-2004060963-A1 METHOD FOR THE PRODUCTION OF POLYCARBONATES GENERAL ELECTRIC COMPANY (US) 2004-07-22 WO claimed
US-6316575-B1 MELT TRANSESTERIFICATION OF DIOL COMPOUND AND CARBOANTE COMPOUND USING CATALYST COMPRISING A PHOSPHORUS-CONTAINING BASIC COMPOUND QUATERNARY PHOSPHONIUM SALT TO FORM POLYCARBONATE IDEMITSU KOSAN CO., LTD. (JP) 2001-11-13 US claimed
EP-1294793-B9 METHOD FOR PREPARING HIGH MOLECULAR WEIGHT POLYCARBONATE SABIC INNOVATIVE PLASTICS IP (NL) 2011-01-26 EP disclosed
EP-1294793-B1 METHOD FOR PREPARING HIGH MOLECULAR WEIGHT POLYCARBONATE SABIC INNOVATIVE PLASTICS IP (NL) 2010-09-08 EP disclosed
US-7629431-B2 Polycarbonate prepolymer for solid phase polymerization and process for producing polycarbonate IDEMITSU KOSAN CO., LTD. (JP) 2009-12-08 US disclosed
US-20080064847-A1 Oxidative carbonylation; molecular weight control IDEMISU KOSAN CO., LTD. (JP) 2008-03-13 US disclosed
US-7122613-B1 Method for the production of polycarbonates GENERAL ELECTRIC COMPANY (US) 2006-10-17 US disclosed
EP-1578840-A1 METHOD FOR THE PRODUCTION OF POLYCARBONATES General Electric Company (US) 2005-09-28 EP disclosed
WO-2004060963-A1 METHOD FOR THE PRODUCTION OF POLYCARBONATES GENERAL ELECTRIC COMPANY (US) 2004-07-22 WO disclosed
US-6576801-B2 Combining a thermally stable organic base with a crude dihydric phenol in the presence of a sulfonic acid compound; melting dihydric phenol and diester of carbonic acid; mixing with polymerization catalyst; oligomerization, polymerization GENERAL ELECTRIC COMPANY 2003-06-10 US disclosed
US-6228973-B1 REACTING A DIHYDRIC PHENOL AND A DIHYDROCARBYL CARBONATE BY SOLVENT-FREE MELT POLYMERIZATION CATALYZED BY A TETRAORGANOPHOSPHONIUM SALT AND A LOWER CONCENTRATION OF ALKALI/ALKALINE EARTH COMPOUND; BY-PRODUCT INHIBITION GENERAL ELECTRIC COMPANY 2001-05-08 US disclosed
EP-1069146-A1 POLYCARBONATE AND OPTICAL MATERIAL Idemitsu Petrochemical Co., Ltd. (JP) 2001-01-17 EP disclosed
EP-1035150-A1 COPOLYCARBONATE AND PROCESS FOR PRODUCING THE SAME IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2000-09-13 EP disclosed
EP-0702044-B1 Polycarbonate redistribution method GEN ELECTRIC (US) 2000-05-03 EP disclosed
EP-0702044-A1 Polycarbonate redistribution method GENERAL ELECTRIC COMPANY (US) 1996-03-20 EP disclosed
US-5459226-A Melt extrusion in presence of tetraorganophosphonium carboxylate salt GENERAL ELECTRIC COMPANY (US) 1995-10-17 US disclosed
EP-0671428-A1 Method for making polycarbonates GENERAL ELECTRIC COMPANY (US) 1995-09-13 EP disclosed
US-5412061-A Polycarbonate melt condensation synthesis using a tetraorganophosphonium carboxylate salt catalyst GENERAL ELECTRIC COMPANY (US) 1995-05-02 US disclosed