SCHEMBL4135265

SCHEMBL4135265

Cc1cc(N2CCN(C(=O)OC(C)(C)C)CC2)cc2[nH]c(-c3c(NCC(O)c4cccc(Cl)c4)cc[nH]c3=O)nc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
IGF1R P08069 20/20 1.00
CYP3A4 P08684 18/20 1.00
EGFR P00533 2/20 0.77
INSR P06213 2/20 0.77
LCK P06239 2/20 0.77
KDR P35968 2/20 0.77
PTK2 Q05397 2/20 0.77
ERBB2 P04626 1/20 0.77
CYP1A2 P05177 1/20 0.77
MET P08581 1/20 0.77
CYP2C9 P11712 1/20 0.77
CYP2C19 P33261 1/20 0.77
MAP2K1 Q02750 1/20 0.77
PLK4 O00444 1/20 0.77
CHEK1 O14757 1/20 0.77
AURKA O14965 1/20 0.77
PDPK1 O15530 1/20 0.77
DAPK3 O43293 1/20 0.77
DYRK3 O43781 1/20 0.77
JAK2 O60674 1/20 0.77

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
SCHEMBL5136723 1.00 IGF1R (1.00) IGF1RCYP3A4EGFRINSRLCK
SCHEMBL5135880 0.91 IGF1R (0.83) IGF1RCYP3A4EGFRINSRLCK
SCHEMBL4140465 0.91 IGF1R (1.00) IGF1RCYP3A4EGFRINSRLCK
SCHEMBL5137241 0.91 IGF1R (1.00) IGF1RCYP3A4EGFRINSRLCK
SCHEMBL5136803 0.90 IGF1R (0.89) IGF1RCYP3A4EGFRINSRLCK
SCHEMBL4137806 0.90 IGF1R (0.89) IGF1RCYP3A4EGFRINSRLCK
SCHEMBL5137616 0.90 IGF1R (0.89) IGF1RCYP3A4EGFRINSRLCK
SCHEMBL5072441 0.90 IGF1R (0.89) IGF1RCYP3A4EGFRINSRLCK
SCHEMBL4142141 0.90 IGF1R (1.00) IGF1RCYP3A4EGFRINSRLCK
SCHEMBL5138466 0.90 IGF1R (1.00) IGF1RCYP3A4EGFRINSRLCK

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
EP-1381598-A4 NOVEL TYROSINE KINASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2008-03-19 EP claimed
US-20040044203-A1 Novel tyrosine kinase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2004-03-04 US claimed
EP-1381598-A1 NOVEL TYROSINE KINASE INHIBITORS Bristol-Myers Squibb Company (US) 2004-01-21 EP claimed
WO-2002079192-A1 NOVEL TYROSINE KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2002-10-10 WO claimed
EP-1670416-A4 METHODS FOR TREATING IGF1R-INHIBITOR INDUCED HYPERGLYCEMIA BRISTOL MYERS SQUIBB CO (US) 2009-06-10 EP disclosed
EP-1381598-A4 NOVEL TYROSINE KINASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2008-03-19 EP disclosed
US-7223757-B2 Tyrosine kinase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-05-29 US disclosed
EP-1758564-A2 SYNERGISTIC METHODS AND COMPOSITIONS FOR TREATING CANCER Brystol-Myers Squibb Company (US) 2007-03-07 EP disclosed
US-7081454-B2 Tyrosine kinase inhibitors BRISTOL-MYERS SQUIBB CO. (US) 2006-07-25 US disclosed
EP-1670416-A2 METHODS FOR TREATING IGF1R-INHIBITOR INDUCED HYPERGLYCEMIA Bristol-Myers Squibb Company (US) 2006-06-21 EP disclosed
US-20060079518-A1 Novel tyrosine kinase inhibitors WITTMAN MARK D 2006-04-13 US disclosed
WO-2005094376-A2 SYNERGISTIC METHODS AND COMPOSITIONS FOR TREATING CANCER BRISTOL-MYERS SQUIBB COMPANY (US) 2005-10-13 WO disclosed
US-20040106605-A1 Synergistic methods and compositions for treating cancer BRISTOL-MYERS SQUIBB COMPANY 2004-06-03 US disclosed
WO-2004031401-A2 NOVEL TYROSINE KINASES INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2004-04-15 WO disclosed
WO-2004030625-A2 SYNERGISTIC METHODS AND COMPOSITIONS FOR TREATING CANCER BRISTOL-MYERS SQUIBB COMPANY (US) 2004-04-15 WO disclosed
WO-2004030627-A2 SYNERGISTIC METHODS AND COMPOSITIONS FOR TREATING CANCER BRISTOL-MYERS SQUIBB COMPANY (US) 2004-04-15 WO disclosed
US-20040072760-A1 Synergistic methods and compositions for treating cancer BRISTOL-MYERS SQUIBB COMPANY 2004-04-15 US disclosed
US-20040044203-A1 Novel tyrosine kinase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2004-03-04 US disclosed
EP-1381598-A1 NOVEL TYROSINE KINASE INHIBITORS Bristol-Myers Squibb Company (US) 2004-01-21 EP disclosed
WO-2002079192-A1 NOVEL TYROSINE KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2002-10-10 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 (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-20040072760-A1 Synergistic methods and compositions for treating cancer IGF1R, MCL1, IGFBP2 IGF1R 1/4885CYP3A4 4799/4885EGFR 13/4885
US-20040044203-A1 Novel tyrosine kinase inhibitors ABL1, YES1, FER IGF1R 216/4885CYP3A4 2334/4885EGFR 45/4885
US-20040106605-A1 Synergistic methods and compositions for treating cancer EGFR, IGF1R, ERBB3 IGF1R 2/4885CYP3A4 4824/4885EGFR 1/4885
US-20060079518-A1 Novel tyrosine kinase inhibitors ABL1, FER, ERBB2 IGF1R 302/4885CYP3A4 2522/4885EGFR 44/4885

“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.