SCHEMBL2208064

SCHEMBL2208064

CC(C)/C=C/CCCCC(=O)O

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PPARG P37231 4/20 0.57
PPARD Q03181 4/20 0.57
PPARA Q07869 4/20 0.57
F7 P08709 4/20 0.57
F3 P13726 4/20 0.57
TERT O14746 3/20 0.57
PTPN1 P18031 3/20 0.57
MAPT P10636 3/20 0.57
BLM P54132 2/20 0.57
HSD17B10 Q99714 2/20 0.57
FABP4 P15090 2/20 0.57
PTGS1 P23219 2/20 0.57
DUSP3 P51452 2/20 0.57
PTPN7 P35236 2/20 0.57
GMNN O75496 1/20 0.57
USP2 O75604 1/20 0.57
LMNA P02545 1/20 0.57
CYP1A2 P05177 1/20 0.57
POLB P06746 1/20 0.57
CYP2C9 P11712 1/20 0.57

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
SCHEMBL2208066 1.00 PPARG (0.57) PPARGPPARDPPARAF7F3
SCHEMBL3338606 1.00 PPARG (0.57) PPARGPPARDPPARAF7F3
SCHEMBL2208737 0.98 PPARG (0.60) PPARGPPARDPPARAF7F3
SCHEMBL22555583 0.98 PPARG (0.60) PPARGPPARDPPARAF7F3
SCHEMBL2206758 0.98 PPARG (0.60) PPARGPPARDPPARAF7F3
SCHEMBL2206876 0.98 PPARG (0.60) PPARGPPARDPPARAF7F3
SCHEMBL2206761 0.98 PPARG (0.60) PPARGPPARDPPARAF7F3
SCHEMBL2208734 0.98 PPARG (0.60) PPARGPPARDPPARAF7F3
SCHEMBL2206883 0.98 PPARG (0.60) PPARGPPARDPPARAF7F3
SCHEMBL2209155 0.94 PPARG (0.52) PPARGPPARDPPARAF7F3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117770450-B High-purity capsaicin composition, and preparation method and application thereof 天津福来特新材料科技有限公司 2024-06-21 CN claimed
EP-3094320-B1 METHODS OF USING CAPSAICIN SYNTHASE FOR THE MICROBIAL PRODUCTION OF CAPSAICINOIDS CONAGEN INC (US) 2023-06-14 EP claimed
US-20230137573-A1 Pharmaceutical Composition for Treating Cancer Comprising Trypsinogen and/or Chymotrypsinogen and an Active Agent Selected from a Selenium Compound, a Vanilloid Compound and a Cytoplasmic Glycolysis Reduction Agent PROPANC PTY LTD (AU) 2023-05-04 US claimed
US-11441162-B2 Human gut microbiome-derived biosynthetic enzymes for production of fatty acid amides MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2022-09-13 US claimed
CN-106456588-B Methods for the microbial production of capsaicinoids using capsaicin synthase 科纳根公司 2021-04-30 CN claimed
US-20200299738-A1 HUMAN GUT MICROBIOME-DERIVED BIOSYNTHETIC ENZYMES FOR PRODUCTION OF FATTY ACID AMIDES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2020-09-24 US claimed
WO-2020185627-A1 HUMAN GUT MICROBIOME-DERIVED BIOSYNTHETIC ENZYMES FOR PRODUCTION OF FATTY ACID AMIDES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2020-09-17 WO claimed
US-10392643-B2 Methods of using acyl-CoA synthetase for biosynthetic production of acyl-CoAs CONAGEN INC. (US) 2019-08-27 US claimed
CN-106419062-B A kind of the automatic lifting adjustable-angle two sides table and its working method of control based on sensory 徐州工程学院 2019-01-29 CN claimed
US-20190010522-A1 METHODS OF MAKING CAPSINOIDS BY BIOSYNTHETIC PROCESSES CONAGEN INC. (US) 2019-01-10 US claimed
US-20070293703-A1 Preparation and purification of synthetic capsaicin ALGORX PHARMACEUTICALS, INC. (US) 2007-12-20 US claimed
EP-1615880-A4 PREPARATION AND PURIFICATION OF SYNTHETIC TRANS CAPSAICIN ALGORX PHARMACEUTICALS INC (US) 2007-03-07 EP claimed
CN-1865234-A Capsicine chemical synthesis and purification method INST OF BIOLOGY SHANDONG ACADE (CN) 2006-11-22 CN claimed
CN-1852707-A Preparation and purification of synthetic capsaicin ALGORX (US) 2006-10-25 CN claimed
CN-1791400-A Composition for lowering lipid in body AJINOMOTO KK (JP) 2006-06-21 CN claimed
EP-1627634-A1 COMPOSITION FOR LOWERING LIPID IN BODY Ajinomoto Co., Inc. (JP) 2006-02-22 EP claimed
EP-1615880-A2 PREPARATION AND PURIFICATION OF SYNTHETIC CAPSAICIN Algorx Pharmaceuticals, Inc. (US) 2006-01-18 EP claimed
US-20050239883-A1 Composition for lowering internal lipid content AJINOMOTO CO., INC. (JP) 2005-10-27 US claimed
US-20050085652-A1 Preparation and purification of synthetic capsaicin ALGORX PHARMACEUTICALS, INC. (US) 2005-04-21 US claimed
WO-2004092122-A2 PREPARATION AND PURIFICATION OF SYNTHETIC CAPSAICIN ALGORX PHARMACEUTICALS, INC. (US) 2004-10-28 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 (5 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-20050085652-A1 Preparation and purification of synthetic capsaicin TRPV1, TRPV5, TAC3 PPARG 2317/4885PPARD 2386/4885PPARA 2004/4885
US-20190010522-A1 METHODS OF MAKING CAPSINOIDS BY BIOSYNTHETIC PROCESSES FADS2, COASY, FASN PPARG 3404/4885PPARD 4130/4885PPARA 3390/4885
US-20230137573-A1 Pharmaceutical Composition for Treating Cancer Comprising Trypsinogen and/or Chymotrypsinogen and an Active Agent Selected from a Selenium Compound, a Vanilloid Compound and a Cytoplasmic Glycolysis Reduction Agent SPINT2, PRSS1, SERPINB1 PPARG 660/4885PPARD 731/4885PPARA 1439/4885
US-20050239883-A1 Composition for lowering internal lipid content PNLIP, LIPC, LIPA PPARG 574/4885PPARD 922/4885PPARA 376/4885
US-20070293703-A1 Preparation and purification of synthetic capsaicin TRPV1, TRPV5, TAC3 PPARG 2317/4885PPARD 2386/4885PPARA 2004/4885

“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.