SCHEMBL3520118

SCHEMBL3520118

CCC(C)N.N#Cc1ccccc1-c1ccc(Cl)cc1

nearest known ligand 0.49

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ESR2 Q92731 1/20 0.49
CNR1 P21554 6/20 0.42
CNR2 P34972 5/20 0.42
PPARG P37231 2/20 0.42
PTPN5 P54829 1/20 0.40
GRIA2 P42262 1/20 0.39
GRIA4 P48058 1/20 0.39
ADORA2A P29274 2/20 0.39
ADORA1 P30542 2/20 0.39
HSD17B3 P37058 1/20 0.39
ACHE P22303 1/20 0.39
CTSA P10619 1/20 0.38
KDM4E B2RXH2 1/20 0.38
ALDH1A1 P00352 1/20 0.38
TDP1 Q9NUW8 1/20 0.38

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
Hydrochloric Acid SCHEMBL4082919 0.99 ESR2 (0.47) ESR2CNR1CNR2PPARGPTPN5
SCHEMBL1541402 0.84 ESR2 (0.66) ESR2CNR1CNR2PTPN5ADORA2A
Hydrochloric Acid SCHEMBL28455839 0.82 ESR2 (0.63) ESR2CNR1CNR2PTPN5ADORA2A
SCHEMBL23742271 0.77 ESR2 (0.53) ESR2PPARGPTPN5GRIA2GRIA4
SCHEMBL8836998 0.76 ESR2 (0.56) ESR2PPARGPTPN5GRIA2GRIA4
SCHEMBL24838568 0.76 ESR2 (0.59) ESR2PPARGPTPN5GRIA2GRIA4
SCHEMBL31410710 0.73 ESR2 (0.76) ESR2PPARGPTPN5GRIA2GRIA4
SCHEMBL360601 0.73 ESR2 (0.59) ESR2CNR2PPARGPTPN5GRIA2
SCHEMBL8244525 0.72 ESR2 (0.54) ESR2CNR2PPARGPTPN5ACHE
Methylamine SCHEMBL3181738 0.71 ESR2 (0.62) ESR2PTPN5GRIA2GRIA4KDM4E

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1575901-B1 SUBSTITUTED AMIDES MERCK SHARP & DOHME (US) 2012-10-10 EP disclosed
US-7667053-B2 Cannabinoid-1 (CB1) receptor antagonists and/or inverse agonists; e.g. N-(2,3-bis(4-chlorophenyl)-1-methylpropyl)-1,4-benzodioxane-2-carboxamide; psychological disorders, eating disorders MERCK & CO., INC. (US) 2010-02-23 US disclosed
US-7576239-B2 Substituted amides MERCK & CO., INC. (US) 2009-08-18 US disclosed
US-7423067-B2 N-(3,4-diphenyl-2-butyl)cyclopentancarboxamide derivatives such as N-(2,3-bis(4-chlorophenyl)-1-methylpropyl)-3-benzoyl-cyclopentane-carboxamide; used for treating conditions including psychological disorders, eating disorders and substance abuse MERCK & CO., INC. (US) 2008-09-09 US disclosed
US-20080194645-A1 Substituted amides MERCK SHARP & DOHME CORP. 2008-08-14 US disclosed
US-7348456-B2 Substituted amides MERCK & CO., INC. (US) 2008-03-25 US disclosed
US-20060106071-A1 Substituted amides MERCK SHARP & DOHME CORP. 2006-05-18 US disclosed
US-20050203112-A1 Bicyclic amides MERCK SHARP & DOHME CORP. 2005-09-15 US disclosed
US-20050154202-A1 Substituted aryl amides MERCK & CO., INC. 2005-07-14 US 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 (4 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-20060106071-A1 Substituted amides CNR1, CNR2, FAAH ESR2 2153/4885CNR1 1/4885CNR2 2/4885
US-20050154202-A1 Substituted aryl amides CNR1, CNR2, FAAH ESR2 1831/4885CNR1 1/4885CNR2 2/4885
US-20050203112-A1 Bicyclic amides CNR1, CNR2, FAAH ESR2 2333/4885CNR1 1/4885CNR2 2/4885
US-20080194645-A1 Substituted amides CNR1, CNR2, FAAH ESR2 2153/4885CNR1 1/4885CNR2 2/4885

“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.