Acetic Acid

Acetic Acid

SCHEMBL2785459

CC(=O)O.COc1ccccc1CNC(=N)Nc1cccc(C#N)n1

nearest known ligand 0.46

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
NR3C2 P08235 1/20 0.46
HPGD P15428 5/20 0.45
ALDH1A1 P00352 3/20 0.45
KMT2A Q03164 5/20 0.44
MEN1 O00255 4/20 0.44
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
GAA P10253 1/20 0.43
MAPT P10636 1/20 0.43
HTT P42858 3/20 0.42
MAOB P27338 1/20 0.42
CHEK1 O14757 1/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
CACNA1B Q00975 1/20 0.41
APBA1 Q02410 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
KDM4E B2RXH2 1/20 0.41
LMNA P02545 1/20 0.41
APEX1 P27695 1/20 0.41
TDP1 Q9NUW8 1/20 0.41

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
SCHEMBL2778559 0.95 ALDH1A1 (0.44) NR3C2HPGDALDH1A1KMT2AMEN1
Acetic Acid SCHEMBL2781484 0.90 LMNA (0.42) HPGDALDH1A1KMT2AMEN1GAA
Acetic Acid SCHEMBL2780357 0.90 RXFP1 (0.39) NR3C2ALDH1A1KMT2AMEN1NPC1
Acetic Acid SCHEMBL2781445 0.89 TAS1R3 (0.41) NR3C2HPGDALDH1A1KMT2AMEN1
Acetic Acid SCHEMBL2780449 0.88 NTRK1 (0.45)
Acetic Acid SCHEMBL2782085 0.86 GRM5 (0.38) NR3C2KMT2AMEN1NPC1RAB9A
Acetic Acid SCHEMBL2781987 0.85 RIPK1 (0.44) NR3C2ALDH1A1KMT2AMEN1CHEK1
Acetic Acid SCHEMBL2783634 0.85 LMNA (0.42) NR3C2ALDH1A1KMT2AGAAMAPT
SCHEMBL2779423 0.84 LMNA (0.41) HPGDALDH1A1KMT2AMEN1GAA
SCHEMBL2782760 0.84 RXFP1 (0.38) NR3C2ALDH1A1KMT2AMEN1NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9296697-B2 Hetaryl-substituted guanidine compounds and use thereof as binding partners for 5-HT5-receptors ABBOTT LABORATORIES (US) 2016-03-29 US disclosed
US-20100184787-A1 Heataryl-substituted guanidine compounds and use thereof as binding partners for 5-ht5-receptors ABBVIE DEUTSCHLAND GMBH & CO KG (DE) 2010-07-22 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-20100184787-A1 Heataryl-substituted guanidine compounds and use thereof as binding partners for 5-ht5-receptors HTR5A, HTR2C, HTR1E NR3C2 620/4885HPGD 1026/4885ALDH1A1 1066/4885

“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.