Acetic Acid

Acetic Acid

SCHEMBL28548169

C=C(C)COc1ccc(Cl)cc1I.CC(=O)[O-].[Na+]

nearest known ligand 0.45

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 16)

geneUniProtsupporting neighboursconfidence
HTR2B P41595 2/20 0.45
HTR2A P28223 1/20 0.45
HTR2C P28335 1/20 0.45
TDP1 Q9NUW8 3/20 0.43
TSHR P16473 1/20 0.43
MAPT P10636 2/20 0.40
MEN1 O00255 1/20 0.40
KMT2A Q03164 1/20 0.40
PTGDR2 Q9Y5Y4 5/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
PTGDR Q13258 1/20 0.40
CYP1A2 P05177 1/20 0.39
CYP2C9 P11712 1/20 0.39
HIF1A Q16665 1/20 0.39
ALDH1A1 P00352 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.39

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
SCHEMBL28542896 0.91 HTR2B (0.51) HTR2BHTR2AHTR2CTDP1TSHR
Acetic Acid SCHEMBL28548166 0.90 TDP1 (0.48) HTR2BHTR2AHTR2CTDP1TSHR
SCHEMBL16427018 0.79 HTR2B (0.48) HTR2BHTR2AHTR2CTDP1TSHR
SCHEMBL1332580 0.77 TDP1 (0.70) TDP1TSHRMAPTPTGDR2PTGDR
SCHEMBL220452 0.77 NPC1 (0.59) HTR2BHTR2AHTR2CTDP1TSHR
SCHEMBL22591956 0.76 TDP1 (0.62) HTR2BHTR2AHTR2CTDP1TSHR
SCHEMBL12035517 0.73 RAB9A (0.49) HTR2BHTR2AHTR2CTDP1TSHR
SCHEMBL3023191 0.73 MGLL (0.49) TSHRMAPTKMT2AALDH1A1
SCHEMBL22695293 0.73 HTR2B (0.46) HTR2BHTR2AHTR2CTDP1TSHR
SCHEMBL9192117 0.73 HTR2B (0.49) HTR2BHTR2AHTR2CTDP1TSHR

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
CN-108047176-B Synthesis method of dihydrobenzofuran compound with chiral quaternary carbon center 常州合全药业有限公司 2021-04-20 CN disclosed