Acetic Acid

Acetic Acid

SCHEMBL4091903

CC(=O)O.COc1cc(C)ccc1O

nearest known ligand 0.59

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
HTT P42858 1/20 0.59
SLC22A6 Q4U2R8 1/20 0.56
SLC22A8 Q8TCC7 1/20 0.56
MEN1 O00255 1/20 0.56
RAB9A P51151 1/20 0.56
KMT2A Q03164 1/20 0.56
TSHR P16473 2/20 0.54
ALDH1A1 P00352 2/20 0.54
TDP1 Q9NUW8 2/20 0.54
NFKB1 P19838 2/20 0.54
GAA P10253 1/20 0.54
MAOB P27338 1/20 0.53
BLM P54132 1/20 0.53
NPSR1 Q6W5P4 1/20 0.53
ACHE P22303 1/20 0.52
CSNK2A1 P68400 2/20 0.51
HSD17B2 P37059 1/20 0.51
APP P05067 1/20 0.51
KDM4E B2RXH2 1/20 0.51
CA12 O43570 1/20 0.51

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
SCHEMBL16913399 0.91 HTT (0.58) HTTSLC22A6SLC22A8MEN1RAB9A
SCHEMBL17629436 0.90 MAOB (0.64) HTTSLC22A6SLC22A8MEN1RAB9A
SCHEMBL29819084 0.90 MAOB (0.64) HTTSLC22A6SLC22A8MEN1RAB9A
SCHEMBL92236 0.90 MAOB (0.64) HTTSLC22A6SLC22A8MEN1RAB9A
Formaldehyde SCHEMBL10355974 0.88 MAOB (0.57) HTTSLC22A6SLC22A8MEN1RAB9A
Hydrochloric Acid SCHEMBL28958540 0.88 MAOB (0.61) HTTSLC22A6SLC22A8MEN1RAB9A
SCHEMBL27940951 0.88 MAOB (0.61) HTTSLC22A6SLC22A8MEN1RAB9A
Bromide SCHEMBL31123050 0.88 MAOB (0.61) HTTSLC22A6SLC22A8MEN1RAB9A
Ethane SCHEMBL28165560 0.88 MAOB (0.61) HTTSLC22A6SLC22A8MEN1RAB9A
Propionic Acid SCHEMBL4084212 0.87 GAA (0.58) HTTSLC22A6SLC22A8MEN1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2237683-B1 METHOD OF FLAVORING GIVAUDAN SA (CH) 2015-11-11 EP disclosed
US-20130177688-A1 Method of Flavoring GIVAUDAN S.A. (CH) 2013-07-11 US disclosed
US-20090186138-A1 Method of Flavoring GIVAUDAN SA (CH) 2009-07-23 US 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-20090186138-A1 Method of Flavoring TAS2R5, TAS2R50, TAS2R10 HTT 2377/4885SLC22A6 1861/4885SLC22A8 1460/4885

“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.