Acetic Acid

Acetic Acid

SCHEMBL5456076

CC(=O)O.COc1cccc2c1CNCC2

nearest known ligand 0.82

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 9)

geneUniProtsupporting neighboursconfidence
PNMT P11086 2/20 0.59
MTNR1A P48039 4/20 0.49
MTNR1B P49286 4/20 0.49
PRCP P42785 1/20 0.48
HRH3 Q9Y5N1 1/20 0.45
NOTUM Q6P988 1/20 0.43
HTR2A P28223 1/20 0.43
HTR2C P28335 1/20 0.43
HTR2B P41595 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
SCHEMBL915092 0.91 PNMT (0.69) PNMTPRCPHRH3HTR2AHTR2C
Hydrochloric Acid SCHEMBL1124672 0.89 PNMT (0.68) PNMTPRCPHRH3HTR2AHTR2C
SCHEMBL5459380 0.84 PNMT (0.50) PNMTPRCPHRH3
Acetic Acid SCHEMBL5459374 0.80 PNMT (0.56) PNMTPRCP
Fumaric Acid SCHEMBL10350879 0.80 HTR2A (0.48) PNMTMTNR1AMTNR1BHTR2AHTR2C
Maleic Acid SCHEMBL10564017 0.80 HTR2A (0.48) PNMTMTNR1AMTNR1BHTR2AHTR2C
SCHEMBL506134 0.79 HTR2C (0.60) PNMTHTR2AHTR2CHTR2B
SCHEMBL31233660 0.78 PNMT (0.56) PNMTHTR2CHTR2B
Hydrochloric Acid SCHEMBL506120 0.78 HTR2C (0.58) PNMTHTR2AHTR2CHTR2B
SCHEMBL2358135 0.78 PNMT (0.56) PNMTHTR2CHTR2B

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
US-20070043024-A1 Azacyclic compounds as inhibitors of sensory neurone specific channels IONIX PHARMACEUTICALS LIMITED (GB) 2007-02-22 US disclosed
EP-1660454-A1 AZACYCLIC COMPOUNDS AS INHIBITORS OF SENSORY NEURONE SPECIFIC CHANNELS Vernalis (R&D) Limited (GB) 2006-05-31 EP disclosed
WO-2005005392-A1 AZACYCLIC COMPOUNDS AS INHIBITORS OF SENSORY NEURONE SPECIFIC CHANNELS IONIX PHARMACEUTICALS LIMITED (GB) 2005-01-20 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-20070043024-A1 Azacyclic compounds as inhibitors of sensory neurone specific channels SCN1B, SCN1A, SCN10A PNMT 429/4885MTNR1A 435/4885MTNR1B 388/4885

“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.