Acetic Acid

Acetic Acid

SCHEMBL7235306

CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].COc1ccc(O)c(-c2ccc(-c3ccc(-c4ccc(C)cc4O)cn3)nc2)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
ESR1 known ✓ P03372 1/20 0.41
KMT2A Q03164 11/20 0.46
MEN1 O00255 9/20 0.46
RAB9A P51151 4/20 0.46
MAPT P10636 3/20 0.46
CASP3 P42574 2/20 0.46
SENP8 Q96LD8 2/20 0.46
SENP7 Q9BQF6 2/20 0.46
SENP6 Q9GZR1 2/20 0.46
LMNA P02545 2/20 0.46
JAK2 O60674 1/20 0.46
NFKB1 P19838 1/20 0.46
NFKB2 Q00653 1/20 0.46
RELA Q04206 1/20 0.46
GAA P10253 5/20 0.43
NPC1 O15118 3/20 0.43
SMN1; SMN2 Q16637 4/20 0.43
ALOX15 P16050 2/20 0.43
KDM4E B2RXH2 2/20 0.43
HPGD P15428 1/20 0.43

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 SCHEMBL7235881 0.95 KMT2A (0.50) KMT2AMEN1RAB9AMAPTCASP3
Acetic Acid SCHEMBL7233241 0.93 KMT2A (0.48) KMT2AMEN1RAB9AMAPTCASP3
Hydrochloric Acid SCHEMBL7238971 0.92 KMT2A (0.50) KMT2AMEN1RAB9AMAPTCASP3
Acetic Acid SCHEMBL7243728 0.89 GAA (0.45) KMT2AMEN1RAB9AMAPTCASP3
Acetic Acid SCHEMBL7242279 0.89 IDO1 (0.42) KMT2AMEN1RAB9AMAPTCASP3
Acetic Acid SCHEMBL7242221 0.87 KMT2A (0.51) KMT2AMEN1RAB9AMAPTCASP3
Acetic Acid SCHEMBL7233180 0.87 GAA (0.40) KMT2AMEN1RAB9AMAPTCASP3
Hydrochloric Acid SCHEMBL7238375 0.86 KMT2A (0.55) KMT2AMEN1RAB9AMAPTCASP3
Acetic Acid SCHEMBL7238175 0.86 RAB9A (0.46) KMT2AMEN1RAB9AMAPTCASP3
Acetic Acid SCHEMBL7243726 0.86 KMT2A (0.42) KMT2AMEN1RAB9AMAPTCASP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
US-6541490-B1 Treating ischemia or reoxygenation injury; preparation from a bipyridine, a benzeneboronic acid and a manganese salt EUKARION, INC. 2003-04-01 US disclosed
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