Acetic Acid

Acetic Acid

SCHEMBL2493436

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nearest known ligand 0.55

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 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 1/20 0.48
GPR119 Q8TDV5 3/20 0.46
RECQL P46063 1/20 0.46
EPHX1 P07099 1/20 0.46
MAPT P10636 2/20 0.45
KDM4E B2RXH2 1/20 0.45
THRB P10828 1/20 0.45
MEN1 O00255 1/20 0.44
ALDH1A1 P00352 1/20 0.44
KMT2A Q03164 1/20 0.44
USP2 O75604 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
USP30 Q70CQ3 2/20 0.43
NR1H2 P55055 1/20 0.42
JAK2 O60674 1/20 0.42
JAK1 P23458 1/20 0.42
HSD17B10 Q99714 1/20 0.42
PTPN2 P17706 1/20 0.42
PTPN1 P18031 1/20 0.42
PTPN6 P29350 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
SCHEMBL8785 0.95 HPGD (0.51) HPGDGPR119RECQLEPHX1MAPT
SCHEMBL322172 0.95 HPGD (0.51) HPGDGPR119RECQLEPHX1MAPT
SCHEMBL241779 0.95 HPGD (0.51) HPGDGPR119RECQLEPHX1MAPT
Carbamic Acid SCHEMBL30731480 0.94 HPGD (0.48) HPGDGPR119RECQLEPHX1MAPT
Hydrochloric Acid SCHEMBL2497038 0.93 HPGD (0.50) HPGDGPR119RECQLEPHX1MAPT
Hydrochloric Acid SCHEMBL861053 0.93 HPGD (0.50) HPGDGPR119RECQLEPHX1MAPT
Hydrochloric Acid SCHEMBL14746009 0.93 HPGD (0.50) HPGDGPR119RECQLEPHX1MAPT
Acetic Acid SCHEMBL6198968 0.90 HPGD (0.54) HPGDGPR119RECQLEPHX1MAPT
Trifluoroacetic Acid SCHEMBL27848482 0.89 HPGD (0.44) HPGDGPR119RECQLEPHX1MAPT
Oxalic Acid SCHEMBL25269098 0.86 MEN1 (0.52) HPGDGPR119RECQLEPHX1MAPT

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-8030501-B2 Process for producing optically active 3-amino nitrogen-containing compounds KANEKA CORPORATION (JP) 2011-10-04 US disclosed
US-20090326246-A1 Method for Production of Optically Active 3-Amino-Nitrogenated Compound KANEKA CORPORATION (JP) 2009-12-31 US disclosed
EP-2050735-A1 METHOD FOR PRODUCTION OF OPTICALLY ACTIVE 3-AMINO-NITROGENATED COMPOUND Kaneka Corporation (JP) 2009-04-22 EP 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-20090326246-A1 Method for Production of Optically Active 3-Amino-Nitrogenated Compound PNMT, NPEPPS, GNMT HPGD 1645/4885GPR119 1183/4885RECQL 4665/4885

“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.