Acetic Acid

Acetic Acid

SCHEMBL31696243

CC(=O)O.NCCCC[C@H](NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CN)C(=O)O

nearest known ligand 0.94

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 14)

geneUniProtsupporting neighboursconfidence
GHSR known ✓ Q92847 1/20 0.45
SLC15A2 Q16348 1/20 0.94
CPB2 Q96IY4 3/20 0.51
SLC6A5 Q9Y345 1/20 0.48
REN P00797 4/20 0.47
ITGB2 P05107 2/20 0.45
ICAM1 P05362 2/20 0.45
ITGAL P20701 2/20 0.45
CPB1 P15086 1/20 0.44
CA1 P00915 1/20 0.43
CA2 P00918 1/20 0.43
CYP3A4 P08684 1/20 0.43
SLC7A5 Q01650 1/20 0.43
EPHX2 P34913 1/20 0.42

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 SCHEMBL29360257 0.99 SLC15A2 (0.92) SLC15A2CPB2SLC6A5RENITGB2
SCHEMBL30175135 0.97 SLC15A2 (1.00) SLC15A2CPB2SLC6A5RENITGB2
SCHEMBL22462015 0.97 SLC15A2 (1.00) SLC15A2CPB2SLC6A5RENITGB2
SCHEMBL19087235 0.97 SLC15A2 (1.00) SLC15A2CPB2SLC6A5RENITGB2
SCHEMBL25354642 0.96 SLC15A2 (0.98) SLC15A2CPB2SLC6A5RENITGB2
SCHEMBL28851961 0.96 SLC15A2 (0.98) SLC15A2CPB2SLC6A5RENITGB2
SCHEMBL29349986 0.94 SLC15A2 (0.94) SLC15A2CPB2SLC6A5RENITGB2
SCHEMBL29352785 0.93 SLC15A2 (0.92) SLC15A2CPB2SLC6A5RENITGB2
SCHEMBL29351224 0.93 SLC15A2 (0.92) SLC15A2CPB2SLC6A5RENITGB2
SCHEMBL22217022 0.88 SLC15A2 (0.79) SLC15A2CPB2SLC6A5RENITGB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250313552-A1 NICOTINATE ESTERS AND THERAPEUTIC METHODS OF USE THEREOF NEW FRONTIER BIO INC (US) 2025-10-09 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-20250313552-A1 NICOTINATE ESTERS AND THERAPEUTIC METHODS OF USE THEREOF NNT, NNMT, NAMPT GHSR 2218/4885SLC15A2 1132/4885CPB2 2332/4885

“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.