Acetic Acid

Acetic Acid

SCHEMBL7874620

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

nearest known ligand 0.48

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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 19)

geneUniProtsupporting neighboursconfidence
CES2 O00748 4/20 0.41
CES1 P23141 4/20 0.41
TSHR P16473 2/20 0.41
MEN1 O00255 3/20 0.40
KMT2A Q03164 3/20 0.40
CYP1A2 P05177 2/20 0.39
ALDH1A1 P00352 2/20 0.39
CYP2D6 P10635 1/20 0.39
CYP2C19 P33261 1/20 0.39
POLB P06746 2/20 0.39
ALPL P05186 1/20 0.39
ALPG P10696 1/20 0.39
LMNA P02545 3/20 0.39
PIN1 Q13526 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
NPC1 O15118 1/20 0.37
CA2 P00918 1/20 0.37
CA4 P22748 1/20 0.37
HSD17B10 Q99714 1/20 0.36

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
Benzoic Acid SCHEMBL7874723 0.86 CA2 (0.57) CES2CES1TSHRMEN1KMT2A
SCHEMBL7871179 0.84 HIF1A (0.42) CES2CES1TSHRMEN1KMT2A
Acetic Acid SCHEMBL133341 0.83 TSHR (0.48) CES2CES1TSHRMEN1KMT2A
Acetic Acid SCHEMBL328882 0.83 TSHR (0.48) CES2CES1TSHRMEN1KMT2A
SCHEMBL7865391 0.82 HIF1A (0.40) CES2CES1TSHRMEN1KMT2A
Hydrochloric Acid SCHEMBL5087717 0.82 HIF1A (0.43) TSHRMEN1KMT2ACYP1A2ALDH1A1
Iodide SCHEMBL2029525 0.82 HIF1A (0.43) TSHRMEN1KMT2ACYP1A2ALDH1A1
Water SCHEMBL2032977 0.82 HIF1A (0.43) TSHRMEN1KMT2ACYP1A2ALDH1A1
Bromide SCHEMBL5088201 0.82 HIF1A (0.43) TSHRMEN1KMT2ACYP1A2ALDH1A1
Acetic Acid SCHEMBL328881 0.82 TSHR (0.47) CES2CES1TSHRMEN1KMT2A

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
US-6316575-B1 MELT TRANSESTERIFICATION OF DIOL COMPOUND AND CARBOANTE COMPOUND USING CATALYST COMPRISING A PHOSPHORUS-CONTAINING BASIC COMPOUND QUATERNARY PHOSPHONIUM SALT TO FORM POLYCARBONATE IDEMITSU KOSAN CO., LTD. (JP) 2001-11-13 US claimed