SCHEMBL2234724

SCHEMBL2234724

COc1cc(OC)c(Cl)c(NC(=O)c2csc3c(Nc4cc(NCCN5CCOCC5)ncn4)ncnc23)c1Cl

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BRAF P15056 7/20 0.41
F2 P00734 1/20 0.41
F10 P00742 1/20 0.41
ABL1 P00519 4/20 0.41
BCR P11274 3/20 0.41
FGFR3 P22607 5/20 0.40
LCK P06239 4/20 0.39
KDR P35968 3/20 0.39
EGFR P00533 1/20 0.39
CYP3A4 P08684 1/20 0.39
AURKA O14965 1/20 0.39
AURKB Q96GD4 1/20 0.39
MAP3K7 O43318 1/20 0.38
ERBB2 P04626 1/20 0.38
JAK2 O60674 2/20 0.38
INSR P06213 2/20 0.38
FYN P06241 2/20 0.38
YES1 P07947 2/20 0.38
LYN P07948 2/20 0.38
RET P07949 2/20 0.38

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
SCHEMBL14137179 0.96 LCK (0.41) BRAFF2F10ABL1BCR
SCHEMBL14057985 0.89 BRAF (0.42) BRAFF2F10LCKKDR
SCHEMBL2232666 0.88 MAP3K7 (0.44) BRAFABL1BCRFGFR3LCK
SCHEMBL14137162 0.86 BRAF (0.40) BRAFF2F10LCKKDR
SCHEMBL2234671 0.85 LCK (0.46) BRAFF2F10FGFR3LCK
SCHEMBL2236433 0.85 F10 (0.51) F2F10FGFR3AURKAFLT3
SCHEMBL14125171 0.84 LCK (0.44) BRAFF2F10ABL1BCR
SCHEMBL14137342 0.84 MAP3K7 (0.42) BRAFABL1BCRFGFR3LCK
SCHEMBL2232539 0.83 HTT (0.43) BRAFF2F10CYP3A4ALDH1A1
SCHEMBL14125254 0.82 LCK (0.48) BRAFF2F10FGFR3LCK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3141552-B1 THIENOPYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE HANMI PHARM IND CO LTD (KR) 2019-04-17 EP claimed
US-10112954-B2 Bicyclic heteroaryl derivatives having inhibitory activity for protein kinase HANMI PHARM. CO., LTD. (KR) 2018-10-30 US claimed
EP-3141552-A1 THIENOPYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE Hanmi Pharm. Co., Ltd. (KR) 2017-03-15 EP claimed
EP-2528920-A2 BICYCLIC HETEROARYL DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE Hanmi Pharm. Co., Ltd. (KR) 2012-12-05 EP claimed
US-20120302567-A1 BICYCLIC HETEROARYL DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2012-11-29 US claimed
WO-2011093672-A2 BICYCLIC HETEROARYL DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE HANMI PHARM. CO., LTD. (KR) 2011-08-04 WO claimed
EP-3141552-B1 THIENOPYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE HANMI PHARM IND CO LTD (KR) 2019-04-17 EP disclosed
US-10112954-B2 Bicyclic heteroaryl derivatives having inhibitory activity for protein kinase HANMI PHARM. CO., LTD. (KR) 2018-10-30 US disclosed
EP-3141552-A1 THIENOPYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE Hanmi Pharm. Co., Ltd. (KR) 2017-03-15 EP disclosed
US-20120302567-A1 BICYCLIC HETEROARYL DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2012-11-29 US disclosed
US-20120302567-A1 BICYCLIC HETEROARYL DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2012-11-29 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 (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-20120302567-A1 BICYCLIC HETEROARYL DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE CDK2, SBK3, CDK2AP1 BRAF 113/4885F2 4328/4885F10 4342/4885
US-10112954-B2 Bicyclic heteroaryl derivatives having inhibitory activity for protein kinase CDK2, SBK3, CDK2AP1 BRAF 113/4885F2 4328/4885F10 4342/4885

“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.