SCHEMBL11931300

SCHEMBL11931300

CC(C)(C)OC(=O)N1CCCC(c2cc(N(COCC[Si](C)(C)C)COCC[Si](C)(C)C)n3ncc(-c4ccc5c(c4)OCO5)c3n2)C1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ SCD5 Q86SK9 1/20 0.39
▸ HPGD P15428 3/20 0.37
▸ KDM4E B2RXH2 1/20 0.37
▸ ALDH1A1 P00352 1/20 0.37
▸ CYP1A2 P05177 1/20 0.37
▸ CYP3A4 P08684 1/20 0.37
▸ CYP2C9 P11712 1/20 0.37
▸ CYP2C19 P33261 1/20 0.37
▸ MAPT P10636 4/20 0.36
▸ TP53 P04637 3/20 0.36
▸ POLB P06746 3/20 0.36
▸ TSHR P16473 2/20 0.36
▸ THRB P10828 1/20 0.36
▸ LMNA P02545 1/20 0.35
▸ GAA P10253 1/20 0.35
▸ MAPK1 P28482 1/20 0.35
▸ CHEK1 O14757 1/20 0.35
▸ PRMT5 O14744 1/20 0.35
▸ CSNK2A2 P19784 1/20 0.34
▸ CSNK2A1 P68400 1/20 0.34

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
SCHEMBL11931292 0.89 PRMT5 (0.39) HPGDKDM4EALDH1A1CYP2C9PRMT5
SCHEMBL14232400 0.89 PRMT5 (0.38) HPGDKDM4EALDH1A1CYP2C9MAPT
SCHEMBL11931293 0.88 CHEK2 (0.40) PRMT5
SCHEMBL14232401 0.88 TRPV3 (0.36) HPGDKDM4EALDH1A1CYP2C9MAPT
SCHEMBL11931295 0.87 PIK3CD (0.41) HPGDPRMT5USP30
SCHEMBL11931298 0.87 EGLN2 (0.39) ALDH1A1MAPTPRMT5
SCHEMBL11931269 0.87 IRAK1 (0.42) CHEK1USP30
SCHEMBL14232399 0.87 CHEK2 (0.36) ALDH1A1MAPTCHEK1PRMT5
SCHEMBL14232398 0.87 ALOX5AP (0.36) CYP2C9PRMT5
SCHEMBL11931294 0.86 GPR119 (0.40) CYP2C9PRMT5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8211854-B2 Methods for inhibiting protein kinases SCHERING CORPORATION (US) 2012-07-03 — — US disclosed
US-20100125068-A1 METHODS FOR INHIBITING PROTEIN KINASES SCHERING CORPORATION 2010-05-20 — — US disclosed
US-7605155-B2 Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors SCHERING CORPORATION (US) 2009-10-20 — — US disclosed
WO-2008045267-A2 PYRAZOLOPYRIMIDINES AS CYCLIN DEPENDENT KINASE INHIBITORS SCHERING CORPORATION (US) 2008-04-17 — — WO disclosed
US-20070082900-A1 Methods for inhibiting protein kinases SCHERING CORPORATION 2007-04-12 — — US disclosed
US-20070072881-A1 Novel pyrazolopyrimidines as cyclin dependent kinase inhibitors SCHERING CORPORATION 2007-03-29 — — 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 (3 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-20070082900-A1 Methods for inhibiting protein kinases PIM1, AURKC, PIM3 SCD5 2820/4885HPGD 3890/4885KDM4E 1092/4885
US-20100125068-A1 METHODS FOR INHIBITING PROTEIN KINASES PIM1, AURKC, PIM3 SCD5 2820/4885HPGD 3890/4885KDM4E 1092/4885
US-20070072881-A1 Novel pyrazolopyrimidines as cyclin dependent kinase inhibitors CDK2, CDK1, CDKN1A SCD5 2508/4885HPGD 1055/4885KDM4E 673/4885

“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.

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