SCHEMBL11930878

SCHEMBL11930878

[O-][n+]1cccc(CNc2cc(N[C@@H]3CCNC[C@@H]3CO)nc3c(Br)cnn23)c1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CDK2 P24941 10/20 0.53
▸ CCNA2 P20248 2/20 0.53
▸ CCNA1 P78396 2/20 0.53
▸ GSK3B P49841 9/20 0.48
▸ CDK1 P06493 8/20 0.47
▸ CDK9 P50750 7/20 0.47
▸ CDK5 Q00535 7/20 0.47
▸ CDK7 P50613 8/20 0.44
▸ CCNE1 P24864 6/20 0.44
▸ CCNH P51946 5/20 0.44
▸ MNAT1 P51948 5/20 0.44
▸ CDK4 P11802 3/20 0.44
▸ CDK6 Q00534 3/20 0.44
▸ GSK3A P49840 2/20 0.44
▸ TAOK1 Q7L7X3 2/20 0.44
▸ CDK8 P49336 2/20 0.44
▸ CCNT1 O60563 1/20 0.44
▸ CCNT2 O60583 1/20 0.44
▸ BRD4 O60885 1/20 0.44
▸ CCNK O75909 1/20 0.44

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
SCHEMBL14276459 0.89 CDK2 (0.55) CDK2CCNA2CCNA1GSK3BCDK1
SCHEMBL12953465 0.89 CDK2 (0.55) CDK2CCNA2CCNA1GSK3BCDK1
SCHEMBL12953874 0.89 CDK2 (0.55) CDK2CCNA2CCNA1GSK3BCDK1
SCHEMBL11930872 0.89 CDK2 (0.55) CDK2CCNA2CCNA1GSK3BCDK1
SCHEMBL14542866 0.89 GSK3B (0.46) CDK2CCNA2CCNA1GSK3BCDK1
SCHEMBL14545790 0.83 CDK2 (0.55) CDK2CCNA2CCNA1GSK3BCDK1
SCHEMBL12953834 0.83 CDK2 (0.63) CDK2CCNA2CCNA1GSK3BCDK1
SCHEMBL13116922 0.82 CDK2 (0.57) CDK2CCNA2CCNA1GSK3BCDK1
SCHEMBL14043213 0.82 GSK3B (0.48) CDK2CCNA2CCNA1GSK3BCDK1
SCHEMBL12954279 0.81 GSK3B (0.71) CDK2CCNA2CCNA1GSK3BCDK1

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
EP-1942900-B1 USE OF PYRAZOLO [1,5-A] PYRIMIDINE DERIVATIVES FOR INHIBITING KINASES METHODS FOR INHIBITING PROTEIN KINASES MERCK SHARP & DOHME (US) 2015-06-03 — — EP disclosed
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
WO-2007044441-A2 USE OF PYRAZOLO [1 , 5 -A] PYRIMIDINE DERIVATIVES FOR INHIBITING PROTEIN KINASES METHODS FOR INHIBITING PROTEIN KINASES SCHERING CORPORATION (US) 2007-04-19 — — WO disclosed
US-20070082900-A1 Methods for inhibiting protein kinases SCHERING CORPORATION 2007-04-12 — — 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 (2 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 CDK2 64/4885CCNA2 1270/4885CCNA1 1142/4885
US-20100125068-A1 METHODS FOR INHIBITING PROTEIN KINASES PIM1, AURKC, PIM3 CDK2 64/4885CCNA2 1270/4885CCNA1 1142/4885

“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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