Decanoic Acid

Decanoic Acid

SCHEMBL629795

CC(O)CO.CCCCCCCCCC(=O)O

nearest known ligand 0.71

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC5A2

The experimentally established mechanism targets of Decanoic 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
GPR84 Q9NQS5 7/20 0.71
PPARG P37231 7/20 0.71
PPARD Q03181 7/20 0.71
PPARA Q07869 7/20 0.71
HDAC11 Q96DB2 5/20 0.71
TSHR P16473 4/20 0.71
PTPN1 P18031 3/20 0.71
FABP4 P15090 3/20 0.71
ALDH1A1 P00352 2/20 0.71
TLR2 O60603 2/20 0.71
TDP1 Q9NUW8 2/20 0.71
FFAR1 O14842 2/20 0.71
FFAR4 Q5NUL3 2/20 0.71
KMT2A Q03164 2/20 0.71
ALOX15 P16050 2/20 0.71
HSD17B10 Q99714 2/20 0.71
SLC22A6 Q4U2R8 1/20 0.71
SLC22A8 Q8TCC7 1/20 0.71
MEN1 O00255 1/20 0.71
ESR1 P03372 1/20 0.71

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 SCHEMBL8658083 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Octanoic Acid SCHEMBL16736954 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Dodecanoate SCHEMBL709152 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Decanoic Acid SCHEMBL6721200 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Palmitic Acid SCHEMBL17075370 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Tridecanoate SCHEMBL16266603 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Dodecanoate SCHEMBL17075372 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Stearic Acid SCHEMBL7858318 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Behenic Acid SCHEMBL22687520 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Stearic Acid SCHEMBL1244008 1.00 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12539313-B2 Microbial removal CAPRETTO EHF. (IS) 2026-02-03 US claimed
EP-3934753-B1 MICROBIAL REMOVAL CAPRETTO EHF (IS) 2025-11-05 EP claimed
US-20250332120-A1 COMPOSITION FOR EXTERNAL PREPARATION KAO CORPORATION (JP) 2025-10-30 US claimed
CN-117224420-B Oil-soluble lip-rounding compound peptide and preparation method thereof 南京斯拜科生物科技股份有限公司 2024-12-31 CN claimed
US-20240156765-A1 METHODS OF NEUROPROTECTION AND USES THEREOF UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION 2024-05-16 US claimed
CN-117771176-A Self-microemulsion composition of lenatinib, drug delivery system and solid preparation 湖南慧泽生物医药科技有限公司 2024-03-29 CN claimed
US-20240050371-A1 W/O/W MICROEMULSIONS FOR OCULAR ADMINISTRATION UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2024-02-15 US claimed
US-11826467-B2 W/O/W microemulsions for ocular administration UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2023-11-28 US claimed
CN-116327759-A Composition containing butylphthalide, edaravone and borneol and compound soft capsule 千乘镜像(北京)科技有限公司 2023-06-27 CN claimed
CN-115955959-A Nanostructured lipid carrier delivery systems, compositions, and methods 康普萨姆公司 2023-04-11 CN claimed
EP-2561865-A2 TRANSDERMAL ABSORPTION PREPARATION Icure Pharmaceutical Inc. (KR) 2013-02-27 EP claimed
CN-101437394-B Cationic antiseptic compositions and methods of use 3M INNOVATIVE PROPERTIES CO 2012-10-10 CN claimed
CN-101437394-A Cationic antiseptic compositions and methods of use 3M INNOVATIVE PROPERTIES CO (US) 2009-05-20 CN claimed
CN-101170985-A Hardenable antimicrobial dental compositions and methods 3M INNOVATIVE PROPERTIES CO (US) 2008-04-30 CN claimed
CN-101048064-A Antimicrobial compositions and methods of use 3M INNOVATIVE PROPERTIES CO (US) 2007-10-03 CN claimed
US-20020165286-A1 Dermal anti-inflammatory composition LEO PHARMACEUTICAL PRODUCTS LTD. A/S (DK) 2002-11-07 US claimed
WO-2002045752-A2 DERMAL ANTI-INFLAMMATORY COMPOSITION LEO PHARMA A/S (DK) 2002-06-13 WO claimed
EP-1117380-A1 GLUCOSIDE PAUCILAMELLAR VESICLES Igen, Inc. (US) 2001-07-25 EP claimed
US-6251425-B1 Glucoside paucilamellar vesicles IGEN, INC. 2001-06-26 US claimed
WO-2000019980-A1 GLUCOSIDE PAUCILAMELLAR VESICLES IGEN, INC. (US) 2000-04-13 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-12539313-B2 Microbial removal CUTA, MIF, PCNA GPR84 2136/4885PPARG 527/4885PPARD 190/4885
US-20240156765-A1 METHODS OF NEUROPROTECTION AND USES THEREOF NLN, BDNF, GAP43 GPR84 2684/4885PPARG 1982/4885PPARD 1929/4885
US-20020165286-A1 Dermal anti-inflammatory composition CUTA, IL1B, LRBA GPR84 1329/4885PPARG 9/4885PPARD 13/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.