Acetic Acid

Acetic Acid

SCHEMBL1948639

CC(=O)O.CC(=O)O.CC(=O)OCCOC(C)=O

nearest known ligand 0.62

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
CHRNB4 known ✓ P30926 1/20 0.55
CHRNA3 known ✓ P32297 1/20 0.55
ALDH1A1 P00352 7/20 0.62
TSHR P16473 2/20 0.62
CHRM5 P08912 2/20 0.55
CHRM1 P11229 2/20 0.55
CHRM3 P20309 2/20 0.55
PGR P06401 1/20 0.55
CHRM2 P08172 1/20 0.55
CHRM4 P08173 1/20 0.55
HTR1A P08908 1/20 0.55
CHRNB2 P17787 1/20 0.55
TBXA2R P21731 1/20 0.55
CHRNA7 P36544 1/20 0.55
CHRNA4 P43681 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
CHRNA10 Q9GZZ6 1/20 0.55
CHRNA9 Q9UGM1 1/20 0.55
LMNA P02545 2/20 0.53
HSD17B10 Q99714 1/20 0.53

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 SCHEMBL6138768 1.00 ALDH1A1 (0.62) ALDH1A1TSHRCHRM5CHRM1CHRM3
Acetic Acid SCHEMBL20681645 1.00 ALDH1A1 (0.62) ALDH1A1TSHRCHRM5CHRM1CHRM3
Acetic Acid SCHEMBL28475084 0.97 ALDH1A1 (0.59) ALDH1A1TSHRCHRM5CHRM1CHRM3
Acetic Acid SCHEMBL10702938 0.94 ALDH1A1 (0.56) ALDH1A1TSHRCHRM5CHRM1CHRM3
SCHEMBL64593 0.93 ALDH1A1 (0.68) ALDH1A1TSHRCHRM5CHRM1CHRM3
Acetic Acid SCHEMBL9717378 0.91 ALDH1A1 (0.68) ALDH1A1TSHRCHRM5CHRM1CHRM3
Benzene SCHEMBL11159553 0.90 ALDH1A1 (0.59) ALDH1A1TSHRCHRM5CHRM1CHRM3
SCHEMBL29446779 0.90 ALDH1A1 (0.65) ALDH1A1TSHRCHRM5CHRM1CHRM3
Ammonia Solution, Strong SCHEMBL5679172 0.90 ALDH1A1 (0.65) ALDH1A1TSHRCHRM5CHRM1CHRM3
Hydrochloric Acid SCHEMBL26134181 0.90 ALDH1A1 (0.65) ALDH1A1TSHRCHRM5CHRM1CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115996927-A Pyrimido [5,4-d ] pyrimidine derivatives and combinations with adenosine receptor antagonists as ENT inhibitors for the treatment of cancer ITEOS比利时公司 2023-04-21 CN claimed
CN-115521175-A Special nutrient solution for vegetables 珠海市现代农业发展中心(珠海市金湾区台湾农民创业园管理委员会、珠海市农渔业科研与推广中心) 2022-12-27 CN claimed
EP-0727491-B1 Enzymatic synthesis of soluble phosphatides from phospholipids LIPOSOME CO INC (US) 1999-06-30 EP claimed
EP-0727491-A1 Enzymatic synthesis of soluble phosphatides from phospholipids THE LIPOSOME COMPANY, INC. (US) 1996-08-21 EP claimed
EP-0528834-A4 ENZYMATIC SYNTHESIS OF SOLUBLE PHOSPHATIDES FROM PHOSPHOLIPIDS 1993-06-02 EP claimed
EP-0528834-A1 ENZYMATIC SYNTHESIS OF SOLUBLE PHOSPHATIDES FROM PHOSPHOLIPIDS. LIPOSOME CO INC (US) 1993-03-03 EP claimed
US-5188951-A Reacting phospholipid with primary alcohol in presence of enzyme catalyst in divalent cationic solution to form divalent salt, reacting formed salt with monovalent cationic salt to form monovalent salt THE LIPOSOME COMPANY, INC. (US) 1993-02-23 US claimed
WO-1991016444-A1 ENZYMATIC SYNTHESIS OF SOLUBLE PHOSPHATIDES FROM PHOSPHOLIPIDS THE LIPOSOME COMPANY, INC. (US) 1991-10-31 WO claimed
EP-4259869-B1 TEXTILE SHEET MATERIAL WACKER CHEMIE AG (DE) 2024-07-03 EP disclosed
US-20240026583-A1 TEXTILE SHEET MATERIAL WACKER CHEMIE AG (DE) 2024-01-25 US disclosed
EP-4259869-A1 TEXTILE SHEET MATERIAL Wacker Chemie AG (DE) 2023-10-18 EP disclosed
CN-103554138-B A kind of have material of organic field effect tube character and preparation method thereof LANZHOU UNIVERSITY (CN) 2016-02-17 CN disclosed
US-8642029-B2 Transiently buffered Lactobacillus preparations and use thereof OSEL, INC. (US) 2014-02-04 US disclosed
US-8329447-B2 Strain of Lactobacillus crispatus OSEL, INC. (US) 2012-12-11 US disclosed
US-20110135615-A1 TRANSIENTLY BUFFERED LACTOBACILLUS PREPARATIONS AND USE THEREOF OSEL, INC. (US) 2011-06-09 US disclosed
US-20100151026-A1 NOVEL STRAIN OF LACTOBACILLUS CRISPATUS OSEL, INC. (US) 2010-06-17 US disclosed
WO-2009123982-A2 TRANSIENTLY BUFFERED LACTOBACILLUS PREPARATIONS AND USE THEREOF OSEL, INC. (US) 2009-10-08 WO disclosed
EP-0630962-A1 Builder system suitable for cleaning agent SARA LEE/DE N.V. (NL) 1994-12-28 EP disclosed
EP-0388389-A2 Improved detergent compositions MONSANTO EUROPE S.A./N.V. (BE) 1990-09-19 EP disclosed