SCHEMBL951985

SCHEMBL951985

CC(C)/C=C/CCCC[C]=O

nearest known ligand 0.33

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TRPV1 Q8NER1 3/20 0.33
ASAH2 Q9NR71 1/20 0.33
MEN1 O00255 5/20 0.32
KMT2A Q03164 5/20 0.32
CYP3A4 P08684 4/20 0.32
PTGS1 P23219 2/20 0.32
PPARG P37231 1/20 0.32
OPRK1 P41145 1/20 0.32
ABCG2 Q9UNQ0 1/20 0.32
MAPT P10636 5/20 0.31
LMNA P02545 4/20 0.31
SMN1; SMN2 Q16637 2/20 0.31
USP2 O75604 1/20 0.31
RECQL P46063 1/20 0.31
MAPK1 P28482 3/20 0.31
ALDH1A1 P00352 3/20 0.31
CYP1A2 P05177 3/20 0.31
CYP2D6 P10635 3/20 0.31
GMNN O75496 2/20 0.31
GLA P06280 2/20 0.31

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
SCHEMBL6058523 1.00 TRPV1 (0.33) TRPV1ASAH2MEN1KMT2ACYP3A4
SCHEMBL951986 0.75 TRPV1 (0.50) TRPV1ASAH2MEN1KMT2ACYP3A4
SCHEMBL6058525 0.75 TRPV1 (0.50) TRPV1ASAH2MEN1KMT2ACYP3A4
SCHEMBL28245143 0.75 TRPV1 (0.36) TRPV1ASAH2MEN1KMT2ACYP3A4
SCHEMBL2162625 0.75
SCHEMBL2162626 0.75
SCHEMBL7287791 0.73 FAAH (0.54) TRPV1MEN1KMT2ACYP3A4PTGS1
SCHEMBL7353526 0.73 FAAH (0.48) TRPV1MEN1KMT2ACYP3A4PTGS1
SCHEMBL2162598 0.73 HMGCR (0.35) TRPV1MEN1KMT2ACYP3A4PTGS1
SCHEMBL2162600 0.73 HMGCR (0.35) TRPV1MEN1KMT2ACYP3A4PTGS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106456588-B Methods for the microbial production of capsaicinoids using capsaicin synthase 科纳根公司 2021-04-30 CN claimed
US-9801850-B2 Antibacterial agent OSAKA UNIVERSITY (JP) 2017-10-31 US claimed
EP-2460405-B1 EPIGALLOCATECHIN GALLATE DERIVATIVE AS ANTIBACTERIAL AGENT UNIV OSAKA (JP) 2015-03-18 EP claimed
EP-2460405-A1 ANTIBACTERIAL AGENT Osaka University (JP) 2012-06-06 EP claimed
US-20120136049-A1 ANTIBACTERIAL AGENT OSAKA UNIVERSITY (JP) 2012-05-31 US claimed
CN-106456588-B Methods for the microbial production of capsaicinoids using capsaicin synthase 科纳根公司 2021-04-30 CN disclosed
US-10655150-B2 Methods of making capsinoids by biosynthetic processes CONAGEN INC. (US) 2020-05-19 US disclosed
US-20190010522-A1 METHODS OF MAKING CAPSINOIDS BY BIOSYNTHETIC PROCESSES CONAGEN INC. (US) 2019-01-10 US disclosed
EP-3377057-A1 METHODS OF MAKING CAPSINOIDS BY BIOSYNTHETIC PROCESSES Conagen Inc. (US) 2018-09-26 EP disclosed
US-9901565-B2 Membrane fusion inhibitor PROTECTEA, LTD. (JP) 2018-02-27 US disclosed
US-9801850-B2 Antibacterial agent OSAKA UNIVERSITY (JP) 2017-10-31 US disclosed
WO-2017120473-A1 METHODS OF MAKING CAPSINOIDS BY BIOSYNTHETIC PROCESSES CONAGEN INC. (US) 2017-07-13 WO disclosed
EP-2460405-A1 ANTIBACTERIAL AGENT Osaka University (JP) 2012-06-06 EP disclosed
US-20120136049-A1 ANTIBACTERIAL AGENT OSAKA UNIVERSITY (JP) 2012-05-31 US disclosed
US-20110003889-A1 MEMBRANE FUSION INHIBITOR KAIHATSU, Kunihiro (JP) 2011-01-06 US disclosed
EP-1069105-B1 CAPSAICINOIDE-LIKE SUBSTANCES HAVING ESTER BOND AJINOMOTO KK (JP) 2007-09-19 EP disclosed
WO-2006038049-A1 A SPRAY FORMULATION FOR PUNGENCY ENHANCEMENT IN CAPSICUM COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2006-04-13 WO disclosed
US-20060073121-A1 Spray formulation for pungency enhancement in Capsicum COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2006-04-06 US disclosed
US-6333421-B1 SUBSTANCES HAVING IMMUNOPOTENTIATING AND ENERGY METABOLISM ENHANCING ACTIVITY MORINAGA & CO., LTD. (JP) 2001-12-25 US disclosed
EP-1069105-A1 NOVEL CAPSAICINOIDE-LIKE SUBSTANCES HAVING ESTER BOND MORINAGA & CO., LTD. (JP) 2001-01-17 EP disclosed

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-20060073121-A1 Spray formulation for pungency enhancement in Capsicum CYP51A1, CAPG, CAPRIN1 TRPV1 105/4885ASAH2 165/4885MEN1 4639/4885
US-20190010522-A1 METHODS OF MAKING CAPSINOIDS BY BIOSYNTHETIC PROCESSES FADS2, COASY, FASN TRPV1 1857/4885ASAH2 116/4885MEN1 3280/4885
US-10655150-B2 Methods of making capsinoids by biosynthetic processes FADS2, COASY, FASN TRPV1 1857/4885ASAH2 116/4885MEN1 3280/4885
US-20120136049-A1 ANTIBACTERIAL AGENT TEAD4, ELOVL6, TEAD1 TRPV1 734/4885ASAH2 3144/4885MEN1 4331/4885
US-20110003889-A1 MEMBRANE FUSION INHIBITOR FLOT1, NSF, VAMP7 TRPV1 764/4885ASAH2 3018/4885MEN1 2941/4885

“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.