Acetic Acid

Acetic Acid

SCHEMBL3435922

CC(=O)O.c1ccc2c(c1)CCCC2

nearest known ligand 0.65

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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 12)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.65
NOTUM Q6P988 4/20 0.50
HSD17B3 P37058 1/20 0.47
RIPK1 Q13546 1/20 0.46
MTNR1A P48039 1/20 0.44
MTNR1B P49286 1/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
ALDH1A1 P00352 2/20 0.43
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43
NPC1 O15118 1/20 0.43
RAB9A P51151 1/20 0.43

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 SCHEMBL817975 0.95 TSHR (0.57) TSHRNOTUMHSD17B3RIPK1MTNR1A
Bicarbonate SCHEMBL28735118 0.90 TSHR (0.72) TSHRNOTUMRIPK1SMN1; SMN2ALDH1A1
Oxalic Acid SCHEMBL27358225 0.87 TSHR (0.68) TSHRRIPK1SMN1; SMN2ALDH1A1MEN1
Hydrogen Peroxide SCHEMBL30110573 0.87 TSHR (0.87) TSHRSMN1; SMN2ALDH1A1MEN1KMT2A
Hydrogen Peroxide SCHEMBL298462 0.87 TSHR (0.87) TSHRSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL15412375 0.85 TSHR (0.65) TSHRNOTUMRIPK1SMN1; SMN2ALDH1A1
Carbamic Acid SCHEMBL9011736 0.85 TSHR (0.65) TSHRNOTUMRIPK1SMN1; SMN2ALDH1A1
Methyl Alcohol SCHEMBL9860225 0.84 TSHR (0.81) TSHRNOTUMRIPK1
Benzene SCHEMBL11299980 0.84 TSHR (0.93) TSHR
Acetamide SCHEMBL5312159 0.83 TSHR (0.55) TSHRNOTUMHSD17B3RIPK1MTNR1A

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-8487121-B2 Chromane derivatives as TRPV3 modulators GLENMARK PHARMACEUTICALS S.A. (CH) 2013-07-16 US disclosed
US-20100311778-A1 CHROMANE DERIVATIVES AS TRPV3 MODULATORS GLENMARK PHARMACEUTICALS S.A. (CH) 2010-12-09 US disclosed
EP-2254879-A2 CHROMANE DERIVATIVES AS TRPV3 MODULATORS Glenmark Pharmaceuticals S.A. (CH) 2010-12-01 EP disclosed
WO-2009084034-A2 CHROMANE DERIVATIVES AS TRPV3 MODULATORS GLENMARK PHARMACEUTICALS, S. A. (CH) 2009-07-09 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-20100311778-A1 CHROMANE DERIVATIVES AS TRPV3 MODULATORS TRPV3, TRPV2, TRPV1 TSHR 1286/4885NOTUM 3993/4885HSD17B3 989/4885

“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.