Stearic Acid

Stearic Acid

SCHEMBL8596126

CCCCCCCCCCCCCCCCCC(=O)[O-].C[P+](C)(C)Cc1ccccc1

nearest known ligand 0.53

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Known targets — ChEMBL curated mechanism

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The experimentally established mechanism targets of Stearic 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
CES2 O00748 2/20 0.50
CES1 P23141 2/20 0.50
EPHX2 P34913 1/20 0.50
HDAC3 O15379 1/20 0.50
HDAC4 P56524 1/20 0.50
HDAC1 Q13547 1/20 0.50
HDAC7 Q8WUI4 1/20 0.50
HDAC2 Q92769 1/20 0.50
HDAC10 Q969S8 1/20 0.50
HDAC11 Q96DB2 1/20 0.50
HDAC8 Q9BY41 1/20 0.50
HDAC6 Q9UBN7 1/20 0.50
HDAC9 Q9UKV0 1/20 0.50
HDAC5 Q9UQL6 1/20 0.50
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
PPARG P37231 2/20 0.48
FABP3 P05413 4/20 0.46
CETP P11597 3/20 0.46
PPARA Q07869 1/20 0.45

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
Stearic Acid SCHEMBL8598208 0.87 EPHX2 (0.47) CES2CES1EPHX2HDAC3HDAC4
Stearic Acid SCHEMBL4599006 0.87 CES2 (0.49) CES2CES1EPHX2HDAC3HDAC4
Dodecanoate SCHEMBL30363216 0.83 HDAC3 (0.54) CES2CES1EPHX2HDAC3HDAC4
Decanoic Acid SCHEMBL31119049 0.80 SLC7A5 (0.59) CES2CES1EPHX2HDAC3HDAC4
Decanoic Acid SCHEMBL29031142 0.80 SLC7A5 (0.59) CES2CES1EPHX2HDAC3HDAC4
Stearic Acid SCHEMBL11045268 0.80 HDAC3 (0.51) CES2CES1EPHX2HDAC3HDAC4
Octanoic Acid SCHEMBL18812646 0.80 ASAH1 (0.52) CES2CES1PPARGFABP3PPARA
Dodecanoate SCHEMBL673994 0.80 HDAC3 (0.51) CES2CES1EPHX2HDAC3HDAC4
Stearic Acid SCHEMBL4454939 0.80 HDAC3 (0.51) CES2CES1EPHX2HDAC3HDAC4
Dodecanoate SCHEMBL4454933 0.80 HDAC3 (0.51) CES2CES1EPHX2HDAC3HDAC4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0309794-B1 No-post-cure method of curing polyacrylate polymers ZEON CHEMICALS INC (US) 1998-01-28 EP claimed
EP-0362459-B1 Polyacrylate polymers utilizing substituted urea retarder ZEON CHEMICALS USA INC (US) 1994-08-10 EP claimed
US-5081194-A Quaternary ammonium or phosphonium curing agent ZEON CHEMICALS U.S.A., INC. (US) 1992-01-14 US claimed
US-5079304-A Curable ZEON CHEMICALS U.S.A., INC. (US) 1992-01-07 US claimed
EP-0362459-A1 Polyacrylate polymers utilizing substituted urea retarder Zeon Chemicals USA, Inc. (US) 1990-04-11 EP claimed
EP-0309794-A2 No-post-cure method of curing polyacrylate polymers Zeon Chemicals USA, Inc. (US) 1989-04-05 EP claimed
EP-0309794-B1 No-post-cure method of curing polyacrylate polymers ZEON CHEMICALS INC (US) 1998-01-28 EP disclosed
EP-0362459-B1 Polyacrylate polymers utilizing substituted urea retarder ZEON CHEMICALS USA INC (US) 1994-08-10 EP disclosed
US-5081194-A Quaternary ammonium or phosphonium curing agent ZEON CHEMICALS U.S.A., INC. (US) 1992-01-14 US disclosed
US-5079304-A Curable ZEON CHEMICALS U.S.A., INC. (US) 1992-01-07 US disclosed
US-5008345-A Two-Part Curing System Containing A Metallic Acid Salt And An Ammonium Or Phosphonium Quaternary Salt ZEON CHEMICAL USA, INC. (US) 1991-04-16 US disclosed
EP-0362459-A1 Polyacrylate polymers utilizing substituted urea retarder Zeon Chemicals USA, Inc. (US) 1990-04-11 EP disclosed
EP-0309794-A2 No-post-cure method of curing polyacrylate polymers Zeon Chemicals USA, Inc. (US) 1989-04-05 EP disclosed