SCHEMBL71090

SCHEMBL71090

CC(C)(C)N(C(=O)O)c1ccnc(Cl)c1

nearest known ligand 0.41

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
SMARCA2 P51531 9/20 0.41
SMARCA4 P51532 8/20 0.41
GRM5 P41594 2/20 0.40
KDM4E B2RXH2 1/20 0.39
ALDH1A1 P00352 1/20 0.39
CNR2 P34972 1/20 0.36
ATR Q13535 1/20 0.36
RECQL P46063 1/20 0.36
KDM5A P29375 1/20 0.35
KDM5B Q9UGL1 1/20 0.35
AR P10275 1/20 0.34
FFAR1 O14842 1/20 0.34
AKR1C3 P42330 1/20 0.33
AKR1C2 P52895 1/20 0.33
TRPA1 O75762 1/20 0.33

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
SCHEMBL27671792 0.86 GRM5 (0.40) SMARCA2SMARCA4GRM5KDM4EALDH1A1
SCHEMBL1459501 0.84 CCNC (0.44) SMARCA2SMARCA4GRM5KDM4EALDH1A1
SCHEMBL2326367 0.81 GRM5 (0.34) SMARCA2SMARCA4GRM5KDM4EALDH1A1
SCHEMBL25216054 0.81 AR (0.45) GRM5KDM4EALDH1A1CNR2KDM5A
SCHEMBL17503398 0.78 ALDH1A1 (0.37) SMARCA2SMARCA4KDM4EALDH1A1KDM5A
SCHEMBL1400929 0.78 ALDH1A1 (0.46) SMARCA2SMARCA4GRM5KDM4EALDH1A1
SCHEMBL1163343 0.77 ALDH1A1 (0.41) SMARCA2SMARCA4GRM5ALDH1A1
SCHEMBL1137155 0.77 SMARCA2 (0.33) SMARCA2SMARCA4GRM5ALDH1A1AR
SCHEMBL3831425 0.75 CHRM5 (0.41) KDM4E
SCHEMBL1351820 0.75 KMT2A (0.46) ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8008317-B2 Inhibitors of akt activtiy MERCK SHARP & DOHME CORP. (US) 2011-08-30 US disclosed
US-7910561-B2 Cancer; such as 3-phenyl-2-(4-{[4-(5-pyridin-2-yl-1H-1,2,4-triazol-3-yl)piperidin-1-yl]methyl}phenyl)-1,6-naphthyridin-5(6H)-one; serine/threonine kinase (Akt) suppression; increased cellular potency or solubility, greater selectivity, enhanced pharmacokinetic properties, lack of off target activity MERCK SHARP & DOHME CORP. (US) 2011-03-22 US disclosed
EP-1814871-B1 COMPOUNDS THAT MODULATE PPARY TYPE RECEPTORS, AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS GALDERMA RES & DEV (FR) 2011-03-02 EP disclosed
US-20040235867-A1 Tyrosine kinase inhibitors BILODEAU MARK T (US) 2004-11-25 US disclosed
WO-2003009852-A1 TYROSINE KINASE INHIBITORS MERCK & CO., INC. (US) 2003-02-06 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 (1 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-20040235867-A1 Tyrosine kinase inhibitors ERBB2, TYRO3, TIE1 SMARCA2 3808/4885SMARCA4 3542/4885GRM5 1726/4885

“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.