SCHEMBL1146860

SCHEMBL1146860

Cc1nc(Cl)cc(Nc2ncc(C(=O)Nc3c(C)cccc3Cl)s2)n1

nearest known ligand 0.85

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LCK P06239 16/20 0.85
ABL1 P00519 5/20 0.85
SRC P12931 5/20 0.85
MAPK14 Q16539 4/20 0.85
EGFR P00533 3/20 0.85
FYN P06241 3/20 0.85
YES1 P07947 3/20 0.85
LYN P07948 3/20 0.85
HCK P08631 3/20 0.85
KIT P10721 3/20 0.85
BCR P11274 3/20 0.85
MAPK13 O15264 2/20 0.85
ERBB2 P04626 2/20 0.85
FGR P09769 2/20 0.85
JAK3 P52333 2/20 0.85
MAPK12 P53778 2/20 0.85
MAPK11 Q15759 2/20 0.85
EPHB6 O15197 2/20 0.67
CSF1R P07333 2/20 0.67
RET P07949 2/20 0.67

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
SCHEMBL29355730 1.00 LCK (0.85) LCKABL1SRCMAPK14EGFR
SCHEMBL1704860 0.95 LCK (0.76) LCKABL1SRCMAPK14EGFR
SCHEMBL20633284 0.95 LCK (0.76) LCKABL1SRCMAPK14EGFR
SCHEMBL4233014 0.94 LCK (0.76) LCKABL1SRCMAPK14EGFR
SCHEMBL31060141 0.92 LCK (1.00) LCKABL1SRCMAPK14EGFR
SCHEMBL774220 0.92 LCK (1.00) LCKABL1SRCMAPK14EGFR
SCHEMBL22336669 0.91 LCK (0.84) LCKABL1SRCMAPK14EGFR
SCHEMBL8210337 0.91 LCK (0.84) LCKABL1SRCMAPK14EGFR
SCHEMBL8217094 0.90 LCK (0.82) LCKABL1SRCMAPK14EGFR
SCHEMBL14142183 0.90 LCK (0.82) LCKABL1SRCMAPK14EGFR

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 309 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10800771-B2 Process for the preparation of dasatinib polymorph NATCO PHARMA LIMITED (IN) 2020-10-13 US claimed
CN-111298127-A Composition comprising histamine release-promoting substance and inhibitory compound, and oral solid preparation containing the same 黄泳华 2020-06-19 CN claimed
CN-111053916-A Anti-tumor drug dasatinib-RGD conjugate, preparation method and application thereof 内蒙古医科大学 2020-04-24 CN claimed
US-20190292177-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF DASATINIB POLYMORPH NATCO PHARMA LIMITED (IN) 2019-09-26 US claimed
WO-2018100585-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF DASATINIB POLYMORPH NATCO PHARMA LIMITED (IN) 2018-06-07 WO claimed
WO-2013065063-A1 ANHYDROUS FORM OF DASATINIB, PROCESS FOR ITS PREPARATION AND ITS USE CADILA HEALTHCARE LIMITED (IN) 2013-05-10 WO claimed
EP-3901151-B1 HALOGENATED-HETEROARYL AND OTHER HETEROCYCLIC KINASE INHIBITORS, AND USES THEREOF IOMX THERAPEUTICS AG (DE) 2026-04-01 EP disclosed
EP-3643713-B1 HETEROCYCLIC KINASE INHIBITORS AND USES THEREOF IOMX THERAPEUTICS AG (DE) 2025-07-30 EP disclosed
US-20250163075-A1 HETEROBIFUNCTIONAL TARGETED PROTEIN DEGRADERS MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2025-05-22 US disclosed
US-20250101015-A1 HETEROCYCLIC KINASE INHIBITORS AND USES THEREOF IOMX THERAPEUTICS AG (DE) 2025-03-27 US disclosed
US-20250084076-A1 HETEROCYCLIC KINASE INHIBITORS AND USES THEREOF IOMX THERAPEUTICS AG (DE) 2025-03-13 US disclosed
US-20250064837-A1 TARGET PROTEIN DEGRADATION COMPOUNDS, THEIR ANTI-TUMOR USE, THEIR INTERMEDIATES AND USE OF INTERMEDIATES SHANGHAITECH UNIVERSITY (CN) 2025-02-27 US disclosed
US-12226424-B2 Target protein degradation compounds, their anti-tumor use, their intermediates and use of intermediates SHANGHAITECH UNIVERSITY (CN) 2025-02-18 US disclosed
US-7189854-B2 Cyclic protein tyrosine kinase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-03-13 US disclosed
EP-1711481-A2 PROCESS FOR PREPARING 2-AMINOTHIAZOLE-5-AROMATIC CARBOXAMIDES AS KINASE INHIBITORS Bristol-Myers Squibb Company (US) 2006-10-18 EP disclosed
US-20060211705-A1 'N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-5-thiazolecarboxamides metabolites BRISTOL-MYERS SQUIBB COMPANY 2006-09-21 US disclosed
WO-2006099474-A1 'N-(2-CHLORO-6-METHYLPHENYL)-2-[[6-[4-(2-HYDROXYETHYL)-1-PIPERAZINYL]-2-METHYL-4-PYRIMIDINYL]AMINO]-5-THIAZOLECARBOXAMIDES METABOLITES BRISTOL-MYERS SQUIBB COMPANY (US) 2006-09-21 WO disclosed
US-20060004067-A1 N-(2-chloro-6-methylphenyl)-2-(6-(4-(3-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-carboxamide; high efficiency, high yield process to get 2-aminothiazole-5-carboxamides using halogention reaction; by-products inhibition; anticancer, psoriasis BRISTOL-MYERS SQUIBB COMPANY 2006-01-05 US disclosed
US-20050215795-A1 Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2005-09-29 US disclosed
WO-2005077945-A2 PROCESS FOR PREPARING 2-AMINOTHIAZOLE-5-AROMATIC CARBOXAMIDES AS KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-08-25 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 (10 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-10800771-B2 Process for the preparation of dasatinib polymorph ABL1, NOP56, SRSF6 LCK 314/4885ABL1 1/4885SRC 74/4885
US-20060004067-A1 N-(2-chloro-6-methylphenyl)-2-(6-(4-(3-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-carboxamide; high efficiency, high yield process to get 2-aminothiazole-5-carboxamides using halogention reaction; by-products inhibition; anticancer, psoriasis TYK2, BRAF, ERBB2 LCK 29/4885ABL1 6/4885SRC 55/4885
US-20050215795-A1 Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors MAP3K5, MAP3K2, MAP3K20 LCK 58/4885ABL1 26/4885SRC 54/4885
US-20190292177-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF DASATINIB POLYMORPH NOP56, ABL1, SRSF6 LCK 315/4885ABL1 2/4885SRC 106/4885
US-20250064837-A1 TARGET PROTEIN DEGRADATION COMPOUNDS, THEIR ANTI-TUMOR USE, THEIR INTERMEDIATES AND USE OF INTERMEDIATES UFM1, SUMO1, SUMO2 LCK 3673/4885ABL1 3044/4885SRC 1668/4885
US-12226424-B2 Target protein degradation compounds, their anti-tumor use, their intermediates and use of intermediates UFM1, SUMO1, SUMO2 LCK 3730/4885ABL1 3132/4885SRC 1824/4885
US-20250163075-A1 HETEROBIFUNCTIONAL TARGETED PROTEIN DEGRADERS KLHDC2, KLHL6, KLHL20 LCK 3954/4885ABL1 4051/4885SRC 2577/4885
US-20060211705-A1 'N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-5-thiazolecarboxamides metabolites IL2, TPMT, HNMT LCK 237/4885ABL1 164/4885SRC 1909/4885
US-20250101015-A1 HETEROCYCLIC KINASE INHIBITORS AND USES THEREOF LCK, SRC, CILK1 LCK 1/4885ABL1 8/4885SRC 2/4885
US-20250084076-A1 HETEROCYCLIC KINASE INHIBITORS AND USES THEREOF LCK, SRC, CILK1 LCK 1/4885ABL1 8/4885SRC 2/4885

“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.