SCHEMBL3535513

SCHEMBL3535513

CCS(=O)(=O)c1ccc(-c2cnc(N)c3c(Br)csc23)cc1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 6/20 0.44
EPHB4 P54760 5/20 0.44
BTK Q06187 9/20 0.41
AURKA O14965 3/20 0.41
MAP4K4 O95819 3/20 0.41
ABL1 P00519 3/20 0.41
INSR P06213 3/20 0.41
FYN P06241 3/20 0.41
CSF1R P07333 3/20 0.41
LYN P07948 3/20 0.41
KIT P10721 3/20 0.41
FGFR1 P11362 3/20 0.41
FLT1 P17948 3/20 0.41
AXL P30530 3/20 0.41
BLK P51451 3/20 0.41
NEK2 P51955 3/20 0.41
MAP4K2 Q12851 3/20 0.41
STK3 Q13188 3/20 0.41
ROCK1 Q13464 3/20 0.41
TAOK1 Q7L7X3 3/20 0.41

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
SCHEMBL3526975 0.88 EPHB4 (0.52) KDREPHB4BTKAURKAMAP4K4
SCHEMBL3532129 0.87 EPHB4 (0.49) KDREPHB4BTKAURKAMAP4K4
SCHEMBL3525488 0.80 BTK (0.49) KDREPHB4BTKAURKAMAP4K4
SCHEMBL3534909 0.80 USP7 (0.48) KDREPHB4BTKAURKAMAP4K4
SCHEMBL3529709 0.77 BTK (0.59) KDREPHB4BTKAURKAABL1
SCHEMBL3534163 0.77 BTK (0.55) KDREPHB4BTKMAP4K4ABL1
SCHEMBL3529462 0.77 KDR (0.54) KDRBTKAURKAMAP4K4ABL1
SCHEMBL3535996 0.77 EPHB4 (0.61) KDREPHB4BTKAURKAMAP4K4
SCHEMBL27640566 0.77 BTK (0.42) KDREPHB4BTKAURKAMAP4K4
SCHEMBL3532714 0.77 KDR (0.73) KDREPHB4BTKAURKAMAP4K4

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
US-8273736-B2 Thienopyridine and furopyridine kinase inhibitors ABBOTT LABORATORIES (US) 2012-09-25 US disclosed
US-7737160-B2 Thienopyridine and furopyridine kinase inhibitors ABBOTT LABORATORIES INC. (US) 2010-06-15 US disclosed
US-20100069371-A1 THIENOPYRIDINE AND FUROPYRIDINE KINASE INHIBITORS ABBOTT LABORATORIES (US) 2010-03-18 US disclosed
EP-1648905-B1 THIENOPYRIDINE AND FUROPYRIDINE KINASE INHIBITORS ABBOTT LAB (US) 2008-12-31 EP disclosed
US-20070155776-A1 THIENOPYRIDINE AND FUROPYRIDINE KINASE INHIBITORS ABBVIE INC. 2007-07-05 US disclosed
US-7202363-B2 Thienopyridine and furopyridine kinase inhibitors ABBOTT LABORATORIES (US) 2007-04-10 US disclosed
CN-1856498-A Thienopyridine and furopyridine kinase inhibitors ABBOTT LAB (US) 2006-11-01 CN disclosed
EP-1648905-A1 THIENOPYRIDINE AND FUROPYRIDINE KINASE INHIBITORS Abbott Laboratories (US) 2006-04-26 EP disclosed
US-20050043347-A1 Thienopyridine and furopyridine kinase inhibitors ABBVIE INC. 2005-02-24 US disclosed
WO-2005010009-A1 THIENOPYRIDINE AND FUROPYRIDINE KINASE INHIBITORS ABBOTT LABORATORIES (US) 2005-02-03 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 (3 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-20050043347-A1 Thienopyridine and furopyridine kinase inhibitors ABL1, ERBB2, LCK KDR 494/4885EPHB4 896/4885BTK 103/4885
US-20100069371-A1 THIENOPYRIDINE AND FUROPYRIDINE KINASE INHIBITORS ABL1, ERBB2, LCK KDR 494/4885EPHB4 896/4885BTK 103/4885
US-20070155776-A1 THIENOPYRIDINE AND FUROPYRIDINE KINASE INHIBITORS ABL1, ERBB2, LCK KDR 494/4885EPHB4 896/4885BTK 103/4885

“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.