SCHEMBL2233873

SCHEMBL2233873

CCN(CC)Cc1ccnc(Nc2ncnc3c(C(=O)Nc4c(Cl)c(OC)cc(OC)c4Cl)csc23)c1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
F2 P00734 2/20 0.42
F10 P00742 2/20 0.42
FGFR3 P22607 4/20 0.40
CYP3A4 P08684 2/20 0.40
CYP2C19 P33261 2/20 0.40
BRAF P15056 11/20 0.40
RAF1 P04049 8/20 0.40
CSF1R P07333 5/20 0.38
DDR1 Q08345 5/20 0.38
DDR2 Q16832 5/20 0.38
FGFR1 P11362 4/20 0.38
FGFR4 P22455 4/20 0.37
JAK2 O60674 2/20 0.37
ABL1 P00519 2/20 0.37
INSR P06213 2/20 0.37
LCK P06239 2/20 0.37
FYN P06241 2/20 0.37
YES1 P07947 2/20 0.37
LYN P07948 2/20 0.37
RET P07949 2/20 0.37

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
SCHEMBL14125286 0.96 BRAF (0.42) F2F10FGFR3CYP3A4CYP2C19
SCHEMBL2235359 0.90 KDR (0.37) F2F10FGFR3CYP3A4CYP2C19
SCHEMBL2231740 0.90 SMN1; SMN2 (0.41) F2F10FGFR3CYP3A4CYP2C19
SCHEMBL2233030 0.89 BRAF (0.38) F2F10FGFR3CYP3A4CYP2C19
SCHEMBL2236293 0.89 F10 (0.47) F2F10FGFR3BRAFRAF1
SCHEMBL2234522 0.89 F10 (0.44) F2F10FGFR3CYP3A4CYP2C19
SCHEMBL14137359 0.88 RAF1 (0.39) F2F10BRAFRAF1CSF1R
SCHEMBL2234840 0.88 BRAF (0.40) F2F10FGFR3CYP3A4CYP2C19
SCHEMBL2232445 0.87 BRAF (0.39) F2F10FGFR3CYP3A4CYP2C19
SCHEMBL2233532 0.87 FGFR1 (0.47) FGFR3CYP3A4CYP2C19BRAFFGFR1

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 10 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

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 F2 4328/4885F10 4342/4885FGFR3 437/4885
US-10112954-B2 Bicyclic heteroaryl derivatives having inhibitory activity for protein kinase CDK2, SBK3, CDK2AP1 F2 4328/4885F10 4342/4885FGFR3 437/4885

“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.