SCHEMBL899872

SCHEMBL899872

NC(=O)c1cnc(N[C@@H]2CCCC[C@@H]2N)nc1Nc1cccc(-n2nccn2)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SYK P43405 20/20 1.00
JAK2 O60674 1/20 1.00
LCK P06239 1/20 1.00
YES1 P07947 1/20 1.00
LYN P07948 1/20 1.00
FGR P09769 1/20 1.00
SRC P12931 1/20 1.00
PRKCA P17252 1/20 1.00
FLT3 P36888 1/20 1.00
ZAP70 P43403 1/20 1.00
MAP3K9 P80192 1/20 1.00
KCNH2 Q12809 1/20 1.00
PAK5 Q9P286 1/20 1.00

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
SCHEMBL1352147 1.00 SYK (1.00) SYKJAK2LCKYES1LYN
SCHEMBL14977351 1.00 SYK (1.00) SYKJAK2LCKYES1LYN
SCHEMBL13624896 1.00 SYK (1.00) SYKJAK2LCKYES1LYN
SCHEMBL1353814 1.00 SYK (1.00) SYKJAK2LCKYES1LYN
SCHEMBL900582 1.00 SYK (1.00) SYKJAK2LCKYES1LYN
Hydrochloric Acid SCHEMBL29392320 0.99 SYK (0.98) SYKJAK2LCKYES1LYN
Hydrochloric Acid SCHEMBL900878 0.99 SYK (0.98) SYKJAK2LCKYES1LYN
SCHEMBL1353568 0.98 SYK (1.00) SYKJAK2LCKYES1LYN
SCHEMBL1353566 0.98 SYK (1.00) SYKJAK2LCKYES1LYN
SCHEMBL1353462 0.98 SYK (1.00) SYKJAK2LCKYES1LYN

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 1377 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260097056-A1 SYK ACTIVATORS AND INHIBITORS IN NEURODEGENERATIVE DISEASES UNIV VIRGINIA PATENT FOUNDATION (US) 2026-04-09 US claimed
US-12594421-B2 Compositions and methods for increasing cancer cell sensitivity to alternating electric fields NOVOCURE GMBH (CH) 2026-04-07 US claimed
WO-2025151443-A1 ENDOXIFEN FOR TREATMENT OF RARE CANCERS ATOSSA THERAPEUTICS, INC. (US) 2025-07-17 WO claimed
US-20250186432-A1 SPLEEN TYROSINE KINASE INHIBITOR, COMPOSITION, AND METHODS OF USE PURDUE RESEARCH FOUNDATION 2025-06-12 US claimed
WO-2025052354-A1 SYK INHIBITORS FOR USE IN THE TREATMENT OF IMMUNE CHECKPOINT INHIBITION INDUCED ADVERSE EVENTS ALBERT-LUDWIGS-UNIVERSITÄT FREIBURG (DE) 2025-03-13 WO claimed
EP-4520333-A1 SYK INHIBITORS FOR USE IN THE TREATMENT OF IMMUNE CHECKPOINT INHIBITION INDUCED ADVERSE EVENTS Albert-Ludwigs-Universität Freiburg (DE) 2025-03-12 EP claimed
US-20250025461-A1 TREATMENT OF SEVERE AND UNCOMPLICATED MALARIA NUREX S.R.L. (IT) 2025-01-23 US claimed
EP-4493188-A2 SPLEEN TYROSINE KINASE INHIBITOR, COMPOSITION, AND METHODS OF USE Purdue Research Foundation (US) 2025-01-22 EP claimed
CN-119300822-A Spleen tyrosine kinase inhibitors, compositions, and methods of use 普渡研究基金会 2025-01-10 CN claimed
US-20240398801-A1 TREATMENT OF LEUKEMIA BASED ON LEUKEMIA HIERARCHY IN A PATIENT UNIVERSITY HEALTH NETWORK (CA) 2024-12-05 US claimed
CN-115429883-A Antitumor pharmaceutical composition for combination therapy 首药控股(北京)股份有限公司 2022-12-06 CN claimed
US-20220218659-A1 PI3K/LYN-ACLY Signaling Inhibition INSTITUTE FOR CANCER RESEARCH D/B/A THE RESEARCH INSTITUTE OF FOX CHASE CANCER CENTER 2022-07-14 US claimed
US-20220096818-A1 Compositions And Methods For Increasing Cancer Cell Sensitivity To Alternating Electric Fields BIOPHARMA CREDIT PLC (GB) 2022-03-31 US claimed
WO-2022035723-A1 COMPOSITIONS, PANELS, AND METHODS FOR CHARACTERIZING CHRONIC LYMPHOCYTIC LEUKEMIA THE BROAD INSTITUTE, INC. (US) 2022-02-17 WO claimed
WO-2022029628-A1 COMPOSITIONS AND METHODS FOR INCREASING CANCER CELL SENSITIVITY TO ALTERNATING ELECTRIC FIELDS NOVOCURE GMBH (CH) 2022-02-10 WO claimed
EP-2323993-B1 2,6-DIAMINO- PYRIMIDIN- 5-YL-CARBOXAMIDES AS SYK OR JAK KINASES INHIBITORS PORTOLA PHARM INC (US) 2015-06-03 EP claimed
US-20130252917-A1 COMBINATION THERAPY OF 4-(3-(2H-1,2,3-TRIAZO-2-YL)PHENYLAMINO)-2-((1R,2S)-2-AMINOCYCLOHEXYLAMINO)PYRIMIDINE-5-CARBOXAMIDE AND FLUDARABINE PORTOLA PHARMACEUTICALS, INC. (US) 2013-09-26 US claimed
US-20130244963-A1 COMBINATION THERAPY WITH 4-(3-(2H-1,2,3-TRIAZOL-2-YL)PHENYLAMINO)-2-((1R,2S)-2-AMINOCYCLOHEXYLAMINO)PYRIMIDINE-5-CARBOXAMIDE PORTOLA PHARMACEUTICALS, INC. (US) 2013-09-19 US claimed
WO-2012044936-A1 COMBINATION THERAPY WITH 4-(3-(2H-1,2,3-TRIAZOL-2-YL)PHENYLAMINO)-2-((1R,2S)-2-AMINOCYCLOHEXYLAMINO)PYRIMIDINE-5-CARBOXAMIDE PORTOLA PHARMACEUTICALS, INC. (US) 2012-04-05 WO claimed
US-8063058-B2 Inhibitors of syk and JAK protein kinases PORTOLA PHARMACEUTICALS, INC. (US) 2011-11-22 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 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-20250186432-A1 SPLEEN TYROSINE KINASE INHIBITOR, COMPOSITION, AND METHODS OF USE SYK, BTK, G6PD SYK 1/4885JAK2 27/4885LCK 4/4885
US-20130252917-A1 COMBINATION THERAPY OF 4-(3-(2H-1,2,3-TRIAZO-2-YL)PHENYLAMINO)-2-((1R,2S)-2-AMINOCYCLOHEXYLAMINO)PYRIMIDINE-5-CARBOXAMIDE AND FLUDARABINE BCL9, BCL9L, MCL1 SYK 101/4885JAK2 137/4885LCK 848/4885
US-20130244963-A1 COMBINATION THERAPY WITH 4-(3-(2H-1,2,3-TRIAZOL-2-YL)PHENYLAMINO)-2-((1R,2S)-2-AMINOCYCLOHEXYLAMINO)PYRIMIDINE-5-CARBOXAMIDE SYK, BCL9L, BCL9 SYK 1/4885JAK2 11/4885LCK 26/4885
US-20260097056-A1 SYK ACTIVATORS AND INHIBITORS IN NEURODEGENERATIVE DISEASES SYK, BTK, FYN SYK 1/4885JAK2 464/4885LCK 13/4885
US-12594421-B2 Compositions and methods for increasing cancer cell sensitivity to alternating electric fields PTK2, GSK3B, MTOR SYK 478/4885JAK2 378/4885LCK 189/4885

“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.