Acetic Acid

Acetic Acid

SCHEMBL6076965

CC(=O)O.CCOC(C(=O)NCc1c(F)cc(C(=N)N)cc1F)n1cccc(Nc2ccccc2)c1=O

nearest known ligand 0.35

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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 14)

geneUniProtsupporting neighboursconfidence
OPRK1 known ✓ P41145 2/20 0.33
KLKB1 P03952 5/20 0.35
F2 P00734 6/20 0.34
PRSS1 P07477 6/20 0.34
F10 P00742 5/20 0.34
F7 P08709 2/20 0.34
CDC25B P30305 1/20 0.31
MYC P01106 1/20 0.31
WDR5 P61964 1/20 0.31
TMPRSS15 P98073 2/20 0.31
ITGB3 P05106 1/20 0.31
ITGA2B P08514 1/20 0.31
OPRM1 P35372 1/20 0.31
ATM Q13315 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
Acetic Acid SCHEMBL6078037 0.91 PRSS1 (0.43) KLKB1F2PRSS1F10F7
SCHEMBL6029315 0.89 OPRK1 (0.34) KLKB1OPRK1CDC25BOPRM1ATM
SCHEMBL6029310 0.89 OPRK1 (0.34) KLKB1OPRK1CDC25BOPRM1ATM
SCHEMBL6079216 0.89 PRSS1 (0.44) KLKB1F2PRSS1F10F7
SCHEMBL6031605 0.89 PRSS1 (0.44) KLKB1F2PRSS1F10F7
Acetic Acid SCHEMBL6078758 0.87 F2 (0.42) KLKB1F2PRSS1F10F7
Acetic Acid SCHEMBL6078293 0.86 F2 (0.44) F2PRSS1F10F7OPRK1
Acetic Acid SCHEMBL6077133 0.84 PRSS1 (0.43) F2PRSS1F10F7OPRK1
Acetic Acid SCHEMBL6028984 0.83 F2 (0.39) KLKB1F2PRSS1F10F7
Acetic Acid SCHEMBL6028097 0.82 F10 (0.47) F2PRSS1F10F7OPRK1

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 OPRK1 1963/4885KLKB1 854/4885F2 7/4885

“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.