Acetic Acid

Acetic Acid

SCHEMBL5042300

CC(=O)O.Cc1ccc(C2(C)CC(C)(C)c3ccc(C)cc3O2)c(O)c1

nearest known ligand 0.48

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
FTO Q9C0B1 2/20 0.48
AKR1B1 P15121 1/20 0.33
CSNK2A1 P68400 1/20 0.33
CNR2 P34972 5/20 0.33
CNR1 P21554 4/20 0.33
TRPA1 O75762 3/20 0.33
TRPV1 Q8NER1 2/20 0.33
TRPV3 Q8NET8 2/20 0.33
TRPV4 Q9HBA0 2/20 0.33
TRPV2 Q9Y5S1 2/20 0.33
CYP1A1 P04798 1/20 0.31
CYP1A2 P05177 1/20 0.31
CYP2A6 P11509 1/20 0.31
CYP2B6 P20813 1/20 0.31
SLC6A2 P23975 1/20 0.31
HTR2A P28223 1/20 0.31
SLC6A4 P31645 1/20 0.31
OPRM1 P35372 1/20 0.31
CYP2J2 P51589 1/20 0.31
CYP1B1 Q16678 1/20 0.31

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
SCHEMBL29908705 0.93 FTO (0.54) FTOCNR2CNR1TRPA1TRPV1
SCHEMBL4665594 0.93 FTO (0.54) FTOCNR2CNR1TRPA1TRPV1
SCHEMBL24124089 0.86 FTO (0.50) FTOCNR2CNR1TRPA1TRPV1
SCHEMBL7522231 0.84 FTO (0.53) FTOCNR2CNR1TRPA1TRPV1
SCHEMBL7520930 0.83 FTO (0.52) FTOAKR1B1CNR2CNR1TRPA1
SCHEMBL9008421 0.83 FTO (0.52) FTOAKR1B1CSNK2A1CNR2CNR1
SCHEMBL5042296 0.80 FTO (0.40) FTOAKR1B1LMNANPC1MAPT
SCHEMBL12251392 0.79 FTO (0.42) FTOCNR2CNR1TRPA1TRPV1
SCHEMBL772979 0.77 FTO (0.55) FTOCNR2LMNAMAPTKMT2A
SCHEMBL30717253 0.77 FTO (0.55) FTOCNR2LMNAMAPTKMT2A

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-7425320-B2 Use of guaiol for treating the skin CIBA SPECIALTY CHEMICALS CORP (US) 2008-09-16 US disclosed
US-20050058610-A1 Cosmetic mixtures containing ultraviolet radiation absorber and decoloring agents CIBA SPECIALTY CHEMICALS CORP. 2005-03-17 US disclosed
EP-1432400-A1 USE OF GUAIOL FOR TREATING THE SKIN Ciba SC Holding AG (CH) 2004-06-30 EP disclosed
WO-2003024417-A1 USE OF GUAIOL FOR TREATING THE SKIN CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2003-03-27 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050058610-A1 Cosmetic mixtures containing ultraviolet radiation absorber and decoloring agents TYR, MC1R, UNG FTO 1161/4885AKR1B1 1153/4885CSNK2A1 4513/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.