Acetic Acid

Acetic Acid

SCHEMBL7774802

CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].Cc1ccc(O)c(-c2cccc(-c3cccc(-c4cc(C)ccc4O)n3)n2)c1.[Mn+3]

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
KMT2A Q03164 6/20 0.46
MEN1 O00255 5/20 0.46
NPC1 O15118 4/20 0.46
RAB9A P51151 3/20 0.46
CYP19A1 P11511 1/20 0.45
HPGD P15428 8/20 0.43
MAPT P10636 8/20 0.43
ALOX15 P16050 4/20 0.43
USP2 O75604 2/20 0.43
LMNA P02545 2/20 0.42
CASP3 P42574 2/20 0.41
SENP7 Q9BQF6 2/20 0.41
POLB P06746 2/20 0.41
SMN1; SMN2 Q16637 2/20 0.41
NPSR1 Q6W5P4 2/20 0.41
SENP8 Q96LD8 1/20 0.41
SENP6 Q9GZR1 1/20 0.41
KDM4E B2RXH2 2/20 0.40
GAA P10253 2/20 0.40
ALDH1A1 P00352 1/20 0.40

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 SCHEMBL7774663 0.96 KMT2A (0.43) KMT2AMEN1NPC1RAB9ACYP19A1
SCHEMBL7232844 0.90 CYP19A1 (0.51) KMT2AMEN1NPC1RAB9ACYP19A1
Acetic Acid SCHEMBL7774822 0.89 KMT2A (0.48) KMT2AMEN1NPC1RAB9ACYP19A1
Acetic Acid SCHEMBL7768750 0.89 KMT2A (0.41) KMT2AMEN1NPC1RAB9AHPGD
Hydrochloric Acid SCHEMBL7235387 0.89 CYP19A1 (0.54) KMT2AMEN1NPC1RAB9ACYP19A1
Acetic Acid SCHEMBL7966187 0.87 AOC1 (0.44) KMT2AMEN1NPC1RAB9AHPGD
Acetic Acid SCHEMBL7774634 0.86 KMT2A (0.40) KMT2AMEN1NPC1RAB9AHPGD
SCHEMBL7238502 0.85 CYP19A1 (0.48) KMT2AMEN1NPC1RAB9ACYP19A1
SCHEMBL7774812 0.85 CYP19A1 (0.48) KMT2AMEN1NPC1RAB9ACYP19A1
Acetic Acid SCHEMBL7768764 0.85 NPC1 (0.42) NPC1HPGDMAPTALOX15CASP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1119573-A2 BIPYRIDINE MANGANESE COMPLEXES EUKARION, INC. (US) 2001-08-01 EP claimed
US-6177419-B1 ANTIOXIDANT CHELATE COMPOUNDS FOR PREVENTING OXYGEN FREE RADICAL-ASSOCIATED DISEASES IN MAMMALS; NEUROPROTECTANTS, SUPEROXIDE DISMUTASE (SOD), CATALASE (CAT) AND/OR PEROXIDASE (POD) MIMETICS EUKARION, INC. 2001-01-23 US claimed
WO-2000009512-A2 BIPYRIDINE MANGANESE COMPLEXES EUKARION, INC. (US) 2000-02-24 WO claimed
EP-1119573-A2 BIPYRIDINE MANGANESE COMPLEXES EUKARION, INC. (US) 2001-08-01 EP disclosed
US-6177419-B1 ANTIOXIDANT CHELATE COMPOUNDS FOR PREVENTING OXYGEN FREE RADICAL-ASSOCIATED DISEASES IN MAMMALS; NEUROPROTECTANTS, SUPEROXIDE DISMUTASE (SOD), CATALASE (CAT) AND/OR PEROXIDASE (POD) MIMETICS EUKARION, INC. 2001-01-23 US disclosed
WO-2000009512-A2 BIPYRIDINE MANGANESE COMPLEXES EUKARION, INC. (US) 2000-02-24 WO disclosed