SCHEMBL971337

SCHEMBL971337

CCNC1(C(N)=O)CCN(Cc2ccccc2)CC1

nearest known ligand 0.70

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CYP2D6 P10635 4/20 0.70
ALDH1A1 P00352 2/20 0.70
TSHR P16473 1/20 0.55
NPFFR1 Q9GZQ6 5/20 0.50
NPFFR2 Q9Y5X5 5/20 0.50
OPRK1 P41145 2/20 0.50
OPRM1 P35372 1/20 0.50
OPRD1 P41143 1/20 0.50
KDM4E B2RXH2 1/20 0.48
CHRM2 P08172 1/20 0.48
CHRM3 P20309 1/20 0.48
OPRL1 P41146 1/20 0.48
POLB P06746 1/20 0.47
CYP3A4 P08684 2/20 0.47
HSD17B10 Q99714 1/20 0.47
CYP2C9 P11712 1/20 0.46
CYP2C19 P33261 1/20 0.46
KMT2A Q03164 1/20 0.46
MAPK1 P28482 1/20 0.46

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
SCHEMBL3932598 0.90 CYP2D6 (0.67) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2
SCHEMBL10500511 0.89 CYP2D6 (0.59) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2
SCHEMBL3210066 0.87 CYP2D6 (0.76) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2
Hydrochloric Acid SCHEMBL10500657 0.86 CYP2D6 (0.56) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2
SCHEMBL3934933 0.83 CYP2D6 (1.00) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2
SCHEMBL2996293 0.82 CYP2D6 (0.68) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2
SCHEMBL27669928 0.82 CYP2D6 (0.54) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2
SCHEMBL8892930 0.80 ALDH1A1 (0.62) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2
SCHEMBL3939085 0.80 CYP2D6 (0.65) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2
SCHEMBL7706329 0.80 ALDH1A1 (0.65) CYP2D6ALDH1A1TSHRNPFFR1NPFFR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7872006-B2 Pyrazole compounds having cannabinoid receptor (CB1) antagonizing activity MITSUBISHI TANABE PHARMA CORPORATION (JP) 2011-01-18 US disclosed
US-7572913-B2 Inhibitors of Rho kinase; N-Benzyloxycarbonyl-4-[N''-(tert-butyloxycarbonyl)hydrazino]piperidine; 4-{[N''-(tert-butyloxycarbonyl)-N'-(1'-propyl)]hydrazino}piperidine BIOAXONE THERAPEUTIQUE INC. (CA) 2009-08-11 US disclosed
CN-100478343-C Purine compound and use as cannabinoid receptor ligands PFIZER (US) 2009-04-15 CN disclosed
US-20090048256-A1 Pyrazole Compounds Having Cannabinoid Receptor (CB1) Antagonizing Activity MITSUBISHI TANABE PHARMA CORPORATION (JP) 2009-02-19 US disclosed
CN-100439369-C Purine compounds and their use as cannabinoid receptor ligands PFIZER (US) 2008-12-03 CN disclosed
EP-1951678-A1 PYRAZOLE COMPOUNDS HAVING CANNABINOID RECEPTOR (CB1) ANTAGONIZING ACTIVITY Mitsubishi Tanabe Pharma Corporation (JP) 2008-08-06 EP disclosed
US-20080097097-A1 Process for Preparing Purine Compounds RAGAN JOHN A 2008-04-24 US disclosed
US-7329658-B2 Cannabinoid receptor ligands and uses thereof PFIZER INC (US) 2008-02-12 US disclosed
US-7329658-B2 Cannabinoid receptor ligands and uses thereof PFIZER INC (US) 2008-02-12 US disclosed
US-7329658-B2 Cannabinoid receptor ligands and uses thereof PFIZER INC (US) 2008-02-12 US disclosed
US-20040214837-A1 Cannabinoid receptor ligands and uses thereof PFIZER INC. 2004-10-28 US disclosed
US-20040214837-A1 Cannabinoid receptor ligands and uses thereof PFIZER INC. 2004-10-28 US disclosed
WO-2004069837-A1 PYRAZOLO`1,5-A!`1,3,5!TRIAZINE DERIVATIVES AS CANNABINOID RECEPTOR LIGANDS PFIZER PRODUCTS INC. (US) 2004-08-19 WO disclosed
WO-2004069838-A1 CANNABINOID RECEPTOR LIGANDS AND USES THEREOF PFIZER PRODUCTS INC. (US) 2004-08-19 WO disclosed
US-20040157838-A1 Cannabinoid receptor ligands and uses thereof PFIZER INC 2004-08-12 US disclosed
US-20040157839-A1 Cannabinoid receptor ligands and uses thereof PFIZER INC 2004-08-12 US disclosed
US-20040157839-A1 Cannabinoid receptor ligands and uses thereof PFIZER INC 2004-08-12 US disclosed
US-20040157839-A1 Cannabinoid receptor ligands and uses thereof PFIZER INC 2004-08-12 US disclosed
US-20040092520-A1 Purine compounds and uses thereof PFIZER INC. 2004-05-13 US disclosed
WO-2004037823-A1 PURINE COMPOUNDS AND USES THEREOF AS CANNABINOID RECEPTOR LIGANDS PFIZER PRODUCTS INC. (US) 2004-05-06 WO 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 (6 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-20040157838-A1 Cannabinoid receptor ligands and uses thereof CNR1, CNR2, GPR18 CYP2D6 1363/4885ALDH1A1 1683/4885TSHR 503/4885
US-20040157839-A1 Cannabinoid receptor ligands and uses thereof CNR1, CNR2, GPR18 CYP2D6 1363/4885ALDH1A1 1683/4885TSHR 503/4885
US-20040214837-A1 Cannabinoid receptor ligands and uses thereof CNR1, CNR2, GPR18 CYP2D6 1363/4885ALDH1A1 1683/4885TSHR 503/4885
US-20090048256-A1 Pyrazole Compounds Having Cannabinoid Receptor (CB1) Antagonizing Activity CNR1, CNR2, OPRD1 CYP2D6 477/4885ALDH1A1 1631/4885TSHR 246/4885
US-20080097097-A1 Process for Preparing Purine Compounds PNP, UMPS, HPRT1 CYP2D6 124/4885ALDH1A1 400/4885TSHR 4361/4885
US-20040092520-A1 Purine compounds and uses thereof CNR1, CNR2, P2RY1 CYP2D6 867/4885ALDH1A1 621/4885TSHR 1832/4885

“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.