SCHEMBL2232963

SCHEMBL2232963

COc1cc(OC)c(Cl)c(NC(=O)c2csc3c(Nc4ccc(F)c(F)c4F)ncnc23)c1Cl

nearest known ligand 0.48

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
BRAF P15056 13/20 0.48
RAF1 P04049 7/20 0.48
CSF1R P07333 4/20 0.45
DDR1 Q08345 4/20 0.45
DDR2 Q16832 4/20 0.45
ARAF P10398 1/20 0.45
ERN1 O75460 4/20 0.45
IRAK4 Q9NWZ3 3/20 0.43
CYP2C9 P11712 1/20 0.41
KDR P35968 2/20 0.40
FLT1 P17948 1/20 0.40
RET P07949 1/20 0.39
KIF5B P33176 1/20 0.39
MAPK14 Q16539 1/20 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
SCHEMBL14125263 0.96 BRAF (0.50) BRAFRAF1CSF1RDDR1DDR2
SCHEMBL14137253 0.94 BRAF (0.46) BRAFRAF1CSF1RDDR1DDR2
SCHEMBL2231476 0.88 BRAF (0.47) BRAFRAF1CSF1RDDR1DDR2
SCHEMBL2236374 0.86 RAF1 (0.58) BRAFRAF1CSF1RDDR1DDR2
SCHEMBL14125255 0.85 BRAF (0.47) BRAFRAF1CSF1RDDR1DDR2
SCHEMBL14137183 0.83 BRAF (0.44) BRAFRAF1CSF1RDDR1DDR2
SCHEMBL2233535 0.82 F10 (0.47) IRAK4
SCHEMBL14125273 0.82 RAF1 (0.60) BRAFRAF1CSF1RDDR1DDR2
SCHEMBL2232574 0.82 RAF1 (0.48) BRAFRAF1CSF1RDDR1DDR2
SCHEMBL2234812 0.82 RAF1 (0.56) BRAFRAF1CSF1RDDR1DDR2

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
US-20120302567-A1 BICYCLIC HETEROARYL DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2012-11-29 US 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
EP-2528920-A2 BICYCLIC HETEROARYL DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE Hanmi Pharm. Co., Ltd. (KR) 2012-12-05 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
WO-2011093672-A2 BICYCLIC HETEROARYL DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASE HANMI PHARM. CO., LTD. (KR) 2011-08-04 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 (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 113/4885RAF1 130/4885CSF1R 4274/4885
US-10112954-B2 Bicyclic heteroaryl derivatives having inhibitory activity for protein kinase CDK2, SBK3, CDK2AP1 BRAF 113/4885RAF1 130/4885CSF1R 4274/4885

“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.