Acetic Acid

Acetic Acid

SCHEMBL5042378

CC(=O)O.CCOC(C(=O)NCc1ccc(C#N)cc1)c1c(F)ccc(CN)c1F

nearest known ligand 0.38

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 13)

geneUniProtsupporting neighboursconfidence
KLKB1 P03952 7/20 0.38
KLK1 P06870 1/20 0.37
BACE1 P56817 2/20 0.36
SLC1A3 P43003 1/20 0.36
SLC1A2 P43004 1/20 0.36
EPHX2 P34913 1/20 0.35
VNN1 O95497 2/20 0.34
TPSAB1 Q15661 2/20 0.34
PLG P00747 1/20 0.34
PRSS1 P07477 1/20 0.34
AKR1B1 P15121 1/20 0.34
ROCK2 O75116 1/20 0.34
PPARA Q07869 1/20 0.34

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
SCHEMBL5041938 0.89 EPHX2 (0.38) SLC1A3SLC1A2EPHX2VNN1AKR1B1
SCHEMBL5041935 0.89 EPHX2 (0.38) SLC1A3SLC1A2EPHX2VNN1AKR1B1
SCHEMBL5042003 0.89 EPHX2 (0.36) SLC1A3SLC1A2EPHX2VNN1AKR1B1
SCHEMBL5042001 0.89 EPHX2 (0.36) SLC1A3SLC1A2EPHX2VNN1AKR1B1
SCHEMBL5041534 0.85 HIF1A (0.39) KLKB1SLC1A3SLC1A2EPHX2VNN1
SCHEMBL5041533 0.85 HIF1A (0.39) KLKB1SLC1A3SLC1A2EPHX2VNN1
Acetic Acid SCHEMBL5041850 0.85 F10 (0.43) KLKB1PRSS1
SCHEMBL5043811 0.84 EPHX2 (0.38) SLC1A3SLC1A2EPHX2VNN1AKR1B1
SCHEMBL5043807 0.84 EPHX2 (0.38) SLC1A3SLC1A2EPHX2VNN1AKR1B1
SCHEMBL5038100 0.84 AKR1B1 (0.37) KLKB1KLK1SLC1A3SLC1A2EPHX2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1567498-B1 MANDELIC ACID DERIVATIVES HOFFMANN LA ROCHE (CH) 2008-01-23 EP disclosed
US-7129238-B2 Mandelic acid derivatives HOFFMANN-LA ROCHE INC. (US) 2006-10-31 US disclosed
EP-1567498-A2 MANDELIC ACID DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2005-08-31 EP disclosed
US-20040122057-A1 Novel mandelic acid derivatives HOFFMANN-LA ROCHE INC. 2004-06-24 US disclosed
WO-2004048335-A2 MANDELIC ACID DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2004-06-10 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-20040122057-A1 Novel mandelic acid derivatives F7, F11, F9 KLKB1 216/4885KLK1 340/4885BACE1 2338/4885

“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.