Acetic Acid

Acetic Acid

SCHEMBL9103437

CC(=O)O.CC(C)c1cccc(O)c1

nearest known ligand 0.54

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
ADRB2 known ✓ P07550 1/20 0.44
ADRA2A known ✓ P08913 1/20 0.44
ADRA2B known ✓ P18089 1/20 0.44
ADRA2C known ✓ P18825 1/20 0.44
HIF1A Q16665 4/20 0.54
KDM4E B2RXH2 3/20 0.54
LMNA P02545 3/20 0.54
ALDH1A1 P00352 4/20 0.53
CA2 P00918 3/20 0.53
CA9 Q16790 3/20 0.53
CYP3A4 P08684 3/20 0.53
CA1 P00915 2/20 0.53
ALOX12 P18054 2/20 0.53
HTT P42858 2/20 0.53
CA5A P35218 2/20 0.53
MDM4 O15151 1/20 0.53
TP53 P04637 1/20 0.53
MAPT P10636 1/20 0.53
TYR P14679 1/20 0.53
HPGD P15428 1/20 0.53

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
Hydrogen Peroxide SCHEMBL11040445 0.92 ADRB1 (0.59) HIF1AKDM4ELMNAALDH1A1CA2
SCHEMBL51528 0.89 ADRB1 (0.61) HIF1AKDM4ELMNAALDH1A1CA2
SCHEMBL29426960 0.89 ADRB1 (0.61) HIF1AKDM4ELMNAALDH1A1CA2
Formaldehyde SCHEMBL27575605 0.88 KDM4E (0.57) HIF1AKDM4ELMNAALDH1A1CA2
SCHEMBL6351865 0.87 ADRB1 (0.59) HIF1AKDM4ELMNAALDH1A1CA2
SCHEMBL28741659 0.87 ADRB1 (0.59) HIF1AKDM4ELMNAALDH1A1CA2
Ethane SCHEMBL16736754 0.87 ADRB1 (0.59) HIF1AKDM4ELMNAALDH1A1CA2
SCHEMBL29020581 0.83 ADRB1 (0.55) HIF1AKDM4ELMNAALDH1A1CA2
SCHEMBL27944560 0.83 KDM4E (0.49) HIF1AKDM4ELMNAALDH1A1CA2
SCHEMBL28753521 0.82 KDM4E (0.52) HIF1AKDM4ELMNAALDH1A1CA2

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-8618139-B2 Oxadiazole derivatives as sphingosine 1-phosphate (S1P) receptor modulators ALLERGAN, INC. (US) 2013-12-31 US disclosed
US-20120142739-A1 NOVEL OXADIAZOLE DERIVATIVES AS SPHINGOSINE 1-PHOSPHATE (S1P) RECEPTOR MODULATORS ALLERGAN, INC. (US) 2012-06-07 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-20120142739-A1 NOVEL OXADIAZOLE DERIVATIVES AS SPHINGOSINE 1-PHOSPHATE (S1P) RECEPTOR MODULATORS S1PR3, S1PR1, S1PR2 ADRB2 100/4885ADRA2A 283/4885ADRA2B 168/4885

“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.