SCHEMBL854029

SCHEMBL854029

C[Si](C)(C)C#Cc1cccc(Cl)c1

nearest known ligand 0.57

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
GRM5 P41594 15/20 0.57
KCNH2 Q12809 1/20 0.53
CYP2D6 P10635 1/20 0.42
MAOB P27338 1/20 0.39
ABL1 P00519 1/20 0.37

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
SCHEMBL3614755 0.85 GRM5 (0.39) GRM5CYP2D6
SCHEMBL17552563 0.80 GRM5 (0.50) GRM5KCNH2CYP2D6MAOB
SCHEMBL30707869 0.80 KCNH2 (0.67) GRM5KCNH2CYP2D6MAOB
SCHEMBL4562631 0.80 KCNH2 (0.67) GRM5KCNH2CYP2D6MAOB
SCHEMBL852832 0.79 TSHR (0.38) GRM5
Charcoal, Activated SCHEMBL31286308 0.78 KCNH2 (0.64) GRM5KCNH2CYP2D6MAOB
SCHEMBL23867871 0.78 APP (0.50) GRM5KCNH2CYP2D6
SCHEMBL31349195 0.78 GRM5 (0.56) GRM5
SCHEMBL3347354 0.78 GRM5 (0.56) GRM5
SCHEMBL2697031 0.77 KCNH2 (0.58) GRM5KCNH2CYP2D6MAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119119117-A Method for preparing alkynyl phosphonate by mechanochemical method 贵州民族大学 2024-12-13 CN disclosed
CN-111961052-B Preparation method of gamma-carboline derivative 沈阳师范大学 2022-06-03 CN disclosed
CN-111961052-A Preparation method of gamma-carboline derivative 沈阳师范大学 2020-11-20 CN disclosed
US-9296687-B2 Modulators of HSP70/DnaK function and methods of use thereof FOX CHASE CANCER CENTER (US) 2016-03-29 US disclosed
US-9296687-B2 Modulators of HSP70/DnaK function and methods of use thereof FOX CHASE CANCER CENTER (US) 2016-03-29 US disclosed
US-20140087005-A1 MODULATORS OF HSP70/DNAK FUNCTION AND METHODS OF USE THEREOF FOX CHASE CANCER CENTER (US) 2014-03-27 US disclosed
US-20140087005-A1 MODULATORS OF HSP70/DNAK FUNCTION AND METHODS OF USE THEREOF FOX CHASE CANCER CENTER (US) 2014-03-27 US disclosed
EP-1425010-B8 SUBSTITUTED INDOLES AND THEIR USE AS INTEGRIN ANTAGONISTS JANSSEN PHARMACEUTICALS INC (US) 2012-03-28 EP disclosed
EP-1425010-B1 SUBSTITUTED INDOLES AND THEIR USE AS INTEGRIN ANTAGONISTS ORTHO MCNEIL PHARM INC (US) 2011-10-26 EP disclosed
US-20110189125-A1 Modulators of HSP70/DnaK Function and Methods of Use Thereof TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2011-08-04 US disclosed
US-7241760-B2 Central nervous system disorders; psycholgical disorders; antiepi;eptic agents; schizophrenia; Alzheimer's disease; cognition activators; analgesics HOFFMANN-LA ROCHE INC. (US) 2007-07-10 US disclosed
EP-1670784-A1 HETEROARYL-SUBSTITUTED IMDAZOLE DERIVATIVES AS GLUTAMATE RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2006-06-21 EP disclosed
US-20050250771-A1 Substituted indoles and their use as integrin antagonists 3-DIMENSIONAL PHARMACEUTICALS, INC. 2005-11-10 US disclosed
US-20050209225-A1 Substituted indoles and their use as integrin antagonists 3-DIMENSIONAL PHARMACEUTICALS, INC. 2005-09-22 US disclosed
US-6855722-B2 Substituted indoles and their use as integrin antagonists DIMENSIONAL PHARMACEUTICALS, INC. (US) 2005-02-15 US disclosed
WO-2004111040-A1 HETEROARYL-SUBSTITUTED IMDAZOLE DERIVATIVES AS GLUTAMATE RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2004-12-23 WO disclosed
US-20040254179-A1 Heteroaryl-substituted imidazole derivatives F. HOFFMANN-LA ROCHE AG (CH) 2004-12-16 US disclosed
EP-1425010-A1 SUBSTITUTED INDOLES AND THEIR USE AS INTEGRIN ANTAGONISTS Ortho-McNeil Pharmaceutical, Inc. (US) 2004-06-09 EP disclosed
US-20020169200-A1 Substituted indoles and their use as integrin antagonists 3-DIMENSIONAL PHARMACEUTICALS, INC. 2002-11-14 US disclosed
WO-2002060438-A1 SUBSTITUTED INDOLES AND THEIR USE AS INTEGRIN ANTAGONISTS 3-DIMENSIONAL PHARMACEUTICALS, INC. (US) 2002-08-08 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-20110189125-A1 Modulators of HSP70/DnaK Function and Methods of Use Thereof HSPBP1, HSPE1, HSP90B1 GRM5 4458/4885KCNH2 4502/4885CYP2D6 4519/4885
US-20040254179-A1 Heteroaryl-substituted imidazole derivatives GRIN2A, GRIN2B, GRIK5 GRM5 4/4885KCNH2 167/4885CYP2D6 994/4885
US-20140087005-A1 MODULATORS OF HSP70/DNAK FUNCTION AND METHODS OF USE THEREOF HSPBP1, HSPE1, HSP90B1 GRM5 4458/4885KCNH2 4502/4885CYP2D6 4519/4885
US-20050209225-A1 Substituted indoles and their use as integrin antagonists ITGAV, ITGA5, ITGB5 GRM5 600/4885KCNH2 387/4885CYP2D6 2523/4885
US-20020169200-A1 Substituted indoles and their use as integrin antagonists ITGAV, ITGAL, ITGA5 GRM5 554/4885KCNH2 467/4885CYP2D6 2465/4885
US-20050250771-A1 Substituted indoles and their use as integrin antagonists ITGAV, ITGA5, ITGB5 GRM5 570/4885KCNH2 357/4885CYP2D6 2524/4885

“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.