Butyric Acid

Butyric Acid

SCHEMBL4624196

CCCC(=O)O.CCCCCC(C)C

nearest known ligand 0.57

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ FFAR4 Q5NUL3 2/20 0.57
▸ FFAR1 O14842 2/20 0.57
▸ FFAR3 O14843 1/20 0.56
▸ HDAC3 O15379 1/20 0.56
▸ HDAC1 Q13547 1/20 0.56
▸ HDAC2 Q92769 1/20 0.56
▸ HDAC8 Q9BY41 1/20 0.56
▸ AKR1B1 P15121 1/20 0.56
▸ GPR84 Q9NQS5 7/20 0.54
▸ PPARG P37231 7/20 0.54
▸ PPARD Q03181 7/20 0.54
▸ PPARA Q07869 7/20 0.54
▸ HDAC11 Q96DB2 5/20 0.54
▸ TSHR P16473 4/20 0.54
▸ PTPN1 P18031 3/20 0.54
▸ ALDH1A1 P00352 2/20 0.54
▸ TLR2 O60603 2/20 0.54
▸ TDP1 Q9NUW8 2/20 0.54
▸ FABP4 P15090 2/20 0.54
▸ SLC22A6 Q4U2R8 1/20 0.54

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 SCHEMBL9192458 0.98 FFAR4 (0.60) FFAR4FFAR1FFAR3HDAC3HDAC1
Succinic Acid SCHEMBL9090939 0.93 FFAR4 (0.59) FFAR4FFAR1AKR1B1GPR84PPARG
Valeric Acid SCHEMBL7775558 0.91 AKR1B1 (0.62) FFAR4FFAR1AKR1B1GPR84PPARG
Octanoic Acid SCHEMBL20394180 0.89 FFAR4 (0.71) FFAR4FFAR1AKR1B1GPR84PPARG
Palmitic Acid SCHEMBL7024981 0.89 FFAR4 (0.71) FFAR4FFAR1AKR1B1GPR84PPARG
Sebacic Acid SCHEMBL9091254 0.89 FFAR4 (0.71) FFAR4FFAR1AKR1B1GPR84PPARG
Stearic Acid SCHEMBL10896371 0.89 FFAR4 (0.71) FFAR4FFAR1AKR1B1GPR84PPARG
Behenic Acid SCHEMBL8407766 0.89 FFAR4 (0.71) FFAR4FFAR1AKR1B1GPR84PPARG
Dodecanoate SCHEMBL20394137 0.89 FFAR4 (0.71) FFAR4FFAR1AKR1B1GPR84PPARG
Nonanoate SCHEMBL9821999 0.89 FFAR4 (0.71) FFAR4FFAR1AKR1B1GPR84PPARG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1133688-A4 METHOD OF PREPARING DELTA-9-TETRAHYDROCANNABINOL UNIV MISSISSIPPI (US) 2008-05-07 — — EP disclosed
EP-1472514-A4 METHOD OF PREPARING DELTA-9 TETRAHYDROCANNABINOL UNIV MISSISSIPPI (US) 2006-01-04 — — EP disclosed
EP-1472514-A2 METHOD OF PREPARING DELTA-9 TETRAHYDROCANNABINOL University of Mississippi (US) 2004-11-03 — — EP disclosed
US-6730519-B2 ISOLATION TETRAHYDROCANNIBINOL FROM PLANT EXTRACT; OBTAIN PLANT SAMPLE, CHELATE TETRAHYDROCANNIBINOL TO SOLID SUPPORT, ELUTE AND RECOVER TETRAHYDROCARBANNIOL FROM SUPPORT THE UNIVERSITY OF MISSISSIPPI 2004-05-04 — — US disclosed
WO-2003061563-A2 METHOD OF PREPARING DELTA-9 TETRAHYDROCANNABINOL UNIVERSITY OF MISSISSIPPI (US) 2003-07-31 — — WO disclosed
EP-0744955-B1 CYCLIC HEPTAPEPTIDE ANTI-INFLAMMATORY AGENT UNIV CALIFORNIA (US) 2002-07-31 — — EP disclosed
US-20020086438-A1 Method of preparing delta-9-tetrahydrocannabinol UNIVERSITY OF MISSISSIPPI, THE 2002-07-04 — — US disclosed
US-20020039795-A1 Recovering preferential particle from plants; obtain plant, generate extract, remove solvent from extract, expose extract to flash distillation, recover preferential plant particles ELSOHLY ET AL 2002-04-04 — — US disclosed
US-6365416-B1 EFFICIENT AND ECONOMIC LARGE SCALE PRODUCTION BY SOLVENT EXTRACTION OF CANNABIS WITH NONPOLAR SOLVENT THEN CHROMATOGRAPHY AND VACUUM DISTILATION THE UNIVERSITY OF MISSISSIPPI 2002-04-02 — — US disclosed
EP-1133688-A1 METHOD OF PREPARING DELTA-9-TETRAHYDROCANNABINOL The university of Mississippi (US) 2001-09-19 — — EP disclosed
US-5919926-A ANTIBIOTIC; ANTIINFLAMMATORY AGENT THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1999-07-06 — — US disclosed
EP-0744955-A4 CYCLIC HEPTAPEPTIDE ANTI-INFLAMMATORY AGENT UNIV CALIFORNIA (US) 1998-12-16 — — EP disclosed
US-5688783-A ANTIBIOTICS, ANTIINFLAMMATORY AGENTS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1997-11-18 — — US disclosed
US-5593960-A PRODUCING CYCLOMARIN A FROM FERMENTATION OF STREPTOMYCES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1997-01-14 — — US disclosed
EP-0744955-A1 CYCLIC HEPTAPEPTIDE ANTI-INFLAMMATORY AGENT THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1996-12-04 — — EP disclosed
WO-1995022339-A1 CYCLIC HEPTAPEPTIDE ANTI-INFLAMMATORY AGENT THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1995-08-24 — — WO disclosed
US-5444043-A Cyclic depsipeptide non-steroidal antiinflammatory agent THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1995-08-22 — — US disclosed
US-5380738-A Side effect reduction MONSANTO COMPANY (US) 1995-01-10 — — US disclosed
US-4418193-A Method of producing 2-epi-fortimicin A ABBOTT LABORATORIES (US) 1983-11-29 — — US disclosed
US-4207415-A Method of producing 2-deoxyfortimicin A ABBOTT LABORATORIES (US) 1980-06-10 — — US disclosed
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