Acetic Acid

Acetic Acid

SCHEMBL9848338

CC(=O)O.CC(=O)[O-].CCN(CC)CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1

nearest known ligand 0.50

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
▸ ADRA2A known ✓ P08913 1/20 0.38
▸ SIGMAR1 Q99720 2/20 0.50
▸ CYP1A2 P05177 2/20 0.43
▸ CYP2D6 P10635 2/20 0.43
▸ LMNA P02545 2/20 0.43
▸ ALDH1A1 P00352 2/20 0.43
▸ MAPT P10636 1/20 0.43
▸ CYP3A4 P08684 1/20 0.43
▸ SMN1; SMN2 Q16637 1/20 0.43
▸ TSHR P16473 1/20 0.42
▸ CYP2C19 P33261 1/20 0.42
▸ CHRM2 P08172 2/20 0.41
▸ CHRM1 P11229 2/20 0.41
▸ CHRM4 P08173 1/20 0.41
▸ CHRM3 P20309 1/20 0.41
▸ GAA P10253 2/20 0.40
▸ BCHE P06276 1/20 0.39
▸ ACHE P22303 1/20 0.39
▸ HIF1A Q16665 1/20 0.39
▸ SCN1A P35498 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
Acetic Acid SCHEMBL9549728 0.99 SIGMAR1 (0.51) SIGMAR1CYP1A2CYP2D6LMNAALDH1A1
Phosphoric Acid SCHEMBL9549735 0.87 SIGMAR1 (0.54) SIGMAR1CYP1A2CYP2D6LMNAALDH1A1
Hydrochloric Acid SCHEMBL9549734 0.86 SIGMAR1 (0.61) SIGMAR1CYP1A2CYP2D6LMNAALDH1A1
Bromide SCHEMBL9549787 0.86 SIGMAR1 (0.61) SIGMAR1CYP1A2CYP2D6LMNAALDH1A1
Acetic Acid SCHEMBL9848369 0.85 ALDH1A1 (0.45) SIGMAR1CYP1A2CYP2D6ALDH1A1MAPT
Acetic Acid SCHEMBL9549692 0.84 ALDH1A1 (0.46) SIGMAR1CYP1A2CYP2D6ALDH1A1MAPT
Bromide SCHEMBL9851216 0.81 SIGMAR1 (0.58) SIGMAR1CYP1A2CYP2D6LMNAMAPT
Acetic Acid SCHEMBL9848347 0.81 HTR2A (0.49) SIGMAR1CYP1A2CYP2D6ALDH1A1MAPT
Acetic Acid SCHEMBL7871075 0.80 ALDH1A1 (0.49) CYP1A2CYP2D6ALDH1A1TSHRCYP2C19
Acetic Acid SCHEMBL3786910 0.80 ALDH1A1 (0.49) CYP1A2CYP2D6ALDH1A1TSHRCYP2C19

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
EP-0441243-A2 Precatalyzed catalyst compositions, process for preparing epoxy resins, curable compositions, articles resulting from curing the resultant compositions THE DOW CHEMICAL COMPANY (US) 1991-08-14 — — EP disclosed
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