Acetic Acid

Acetic Acid

SCHEMBL6076473

CC(=O)O.CCNc1cc(C(=N)N)ccc1CNC(=O)C(OCC)N1Cc2c(C)cccc2C1=O

nearest known ligand 0.35

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 11)

geneUniProtsupporting neighboursconfidence
F10 P00742 7/20 0.35
ITGB3 P05106 5/20 0.31
ITGA2B P08514 5/20 0.31
F2 P00734 4/20 0.31
PRSS1 P07477 3/20 0.31
THRB P10828 1/20 0.30
F7 P08709 1/20 0.30
MAPT P10636 1/20 0.30
F9 P00740 1/20 0.30
PRSS2 P07478 1/20 0.30
PRSS3 P35030 1/20 0.30

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
SCHEMBL6079218 0.98 F10 (0.34) F10ITGB3ITGA2BF2PRSS1
SCHEMBL6079242 0.98 F10 (0.34) F10ITGB3ITGA2BF2PRSS1
Acetic Acid SCHEMBL6077490 0.92 F10 (0.37) F10ITGB3ITGA2BF2PRSS1
Acetic Acid SCHEMBL6077426 0.91 F10 (0.35) F10F2PRSS1
SCHEMBL6079438 0.89 F10 (0.38) F10ITGB3ITGA2BF2PRSS1
SCHEMBL6079462 0.89 F10 (0.38) F10ITGB3ITGA2BF2PRSS1
SCHEMBL6077467 0.88 F10 (0.36) F10F2PRSS1THRBMAPT
SCHEMBL6077453 0.88 F10 (0.36) F10F2PRSS1THRBMAPT
Acetic Acid SCHEMBL6077968 0.87 F10 (0.45) F10ITGB3ITGA2BF2PRSS1
Acetic Acid SCHEMBL6079132 0.86 F2 (0.40) F10ITGB3ITGA2BF2PRSS1

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-7056932-B2 Heterocyclyl substituted 1-alkoxy acetic acid amides HOFFMAN-LA ROCHE INC. (US) 2006-06-06 US claimed
US-20050137168-A1 Heterocyclyl substituted 1-alkoxy acetic acid amides HOFFMANN-LA ROCHE INC. 2005-06-23 US claimed
US-7056932-B2 Heterocyclyl substituted 1-alkoxy acetic acid amides HOFFMAN-LA ROCHE INC. (US) 2006-06-06 US disclosed
US-20050137168-A1 Heterocyclyl substituted 1-alkoxy acetic acid amides HOFFMANN-LA ROCHE INC. 2005-06-23 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-20050137168-A1 Heterocyclyl substituted 1-alkoxy acetic acid amides F12, TFPI, F11 F10 8/4885ITGB3 1106/4885ITGA2B 350/4885

“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.