Butyric Acid

Butyric Acid

SCHEMBL600203

CCCC(=O)[O-].CCCC(=O)[O-].[Mn+2]

nearest known ligand 0.93

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Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
FFAR3 O14843 3/20 0.93
HDAC3 O15379 3/20 0.93
HDAC1 Q13547 3/20 0.93
HDAC2 Q92769 3/20 0.93
HDAC8 Q9BY41 3/20 0.93
CA1 P00915 3/20 0.60
CES2 O00748 2/20 0.59
CES1 P23141 2/20 0.59
NFKB1 P19838 1/20 0.48
GPR84 Q9NQS5 1/20 0.46
TSHR P16473 1/20 0.45
FABP3 P05413 2/20 0.44
CA2 P00918 1/20 0.44

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
Butyric Acid SCHEMBL6746198 0.97 FFAR3 (0.88) FFAR3HDAC3HDAC1HDAC2HDAC8
Butyric Acid SCHEMBL1331084 0.93
Butyric Acid SCHEMBL10908702 0.93 FFAR3 (0.93) FFAR3HDAC3HDAC1HDAC2HDAC8
Butyric Acid SCHEMBL6387265 0.93 FFAR3 (0.93) FFAR3HDAC3HDAC1HDAC2HDAC8
Butyric Acid SCHEMBL1330878 0.93
Butyric Acid SCHEMBL11441641 0.93 FFAR3 (0.93) FFAR3HDAC3HDAC1HDAC2HDAC8
Butyric Acid SCHEMBL2587931 0.93 FFAR3 (0.93) FFAR3HDAC3HDAC1HDAC2HDAC8
Butyric Acid SCHEMBL9800297 0.93 FFAR3 (0.93) FFAR3HDAC3HDAC1HDAC2HDAC8
Butyric Acid SCHEMBL4292004 0.93 FFAR3 (1.00) FFAR3HDAC3HDAC1HDAC2HDAC8
Butyric Acid SCHEMBL11419652 0.93 FFAR3 (0.93) FFAR3HDAC3HDAC1HDAC2HDAC8

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 158 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2004065305-A1 NON-TOXIC CORROSION-PROTECTION PIGMENTS BASED ON MANGANESE UNIVERSITY OF DAYTON (US) 2004-08-05 WO claimed
WO-2004065493-A1 NON-TOXIC CORROSION-PROTECTION PIGMENTS BASED ON PERMANGANATES AND MANGANATES (VI) UNIVERSITY OF DAYTON (US) 2004-08-05 WO claimed
US-6695938-B2 Reducing agent in solvent; reactive fuel reacts with hydrogen peroxide oxidizer; high speed ignition THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY 2004-02-24 US claimed
US-20040011252-A1 Non-toxic corrosion-protection pigments based on manganese UNIVERSITY OF DAYTON 2004-01-22 US claimed
US-20030221590-A1 Non-toxic corrosion-protection pigments based on permanganates and manganates UNIVERSITY OF DAYTON 2003-12-04 US claimed
US-20030192633-A1 Reduced toxicity hypergolic bipropellant fuels NAVY, UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE 2003-10-16 US claimed
EP-0813256-B1 Layered, hexagonal lithium manganese oxide as a positive electrode active material for lithium battery, method for producing the same, and lithium battery containing the same JAPAN STORAGE BATTERY CO LTD (JP) 2002-05-08 EP claimed
US-5981106-A Positive electrode active material for lithium battery, method for producing the same, and lithium battery containing the same JAPAN STORAGE BATTERY CO., LTD. (JP) 1999-11-09 US claimed
EP-0655051-B1 PROCESS FOR PREPARING PHENYLTEREPHTHALIC ACID EASTMAN CHEM CO (US) 1998-04-15 EP claimed
EP-0813256-A2 Layered, hexagonal lithium manganese oxide as a positive electrode active material for lithium battery, method for producing the same, and lithium battery containing the same Japan Storage Battery Company Limited (JP) 1997-12-17 EP claimed
US-5334754-A Process for preparing 2,5-diphenylterephthalic acid by oxidation EASTMAN CHEMICAL COMPANY (US) 1994-08-02 US claimed
WO-1994004480-A1 PROCESS FOR PREPARING PHENYLTEREPHTHALIC ACID EASTMAN CHEMICAL COMPANY (US) 1994-03-03 WO claimed
WO-1994004481-A1 PROCESS FOR PREPARING 2,5-DIPHENYLTEREPHTHALIC ACID EASTMAN CHEMICAL COMPANY (US) 1994-03-03 WO claimed
US-5023372-A Manganese salt of carboxylic acid and a phenylenediamine BETZ LABORATORIES, INC. (US) 1991-06-11 US claimed
EP-0398633-A1 Method and compositions for inhibiting polymerization of acrylic acid monomers BETZ EUROPE, INC. (US) 1990-11-22 EP claimed
US-4500719-A Process for the preparation of N-alkenylphenylmaleimides and N,N'-[alkenylenephenylene]bismalemides MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1985-02-19 US claimed
US-4460522-A Method of producing low density oxide fuel pellet DORYOKURO KAKUNENRYO KAIHATSU JIGYODAN (JP) 1984-07-17 US claimed
US-4355173-A Process for the preparation of alkyl carboxylate MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1982-10-19 US claimed
US-4230882-A OXIDATION OF P-XYLENE WITH COBALT-MANGANESE-BROMINE CATALYST SYSTEM ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1980-10-28 US claimed
US-4211882-A OXIDIZING P-TOLUALDEHYDE, CATALYST CONSISTING OF A MANGANESE COMPOUND, A COBALT COMPOUND, A BROMINE COMPOUND, AND A NICKEL, IRON, CHROMIUM, OR LANTHANIDE COMPOUND MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1980-07-08 US claimed