SCHEMBL1312033

SCHEMBL1312033

Cc1ccc(Nc2nc(N[C@@H]3CCOC[C@@H]3N)ncc2C(N)=O)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ SYK P43405 20/20 1.00
▸ MAPK3 P27361 5/20 1.00
▸ MAPK1 P28482 5/20 1.00
▸ KCNH2 Q12809 5/20 1.00
▸ AURKB Q96GD4 5/20 1.00
▸ JAK2 O60674 1/20 1.00
▸ LCK P06239 1/20 1.00
▸ LYN P07948 1/20 1.00
▸ JAK1 P23458 1/20 1.00
▸ ZAP70 P43403 1/20 1.00
▸ JAK3 P52333 1/20 1.00
▸ TYRO3 Q06418 1/20 1.00
▸ EML4 Q9HC35 1/20 0.60
▸ ALK Q9UM73 1/20 0.60

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
Hydrochloric Acid SCHEMBL30189541 0.99 SYK (0.98) SYKMAPK3MAPK1KCNH2AURKB
SCHEMBL19958390 0.92 SYK (0.86) SYKMAPK3MAPK1KCNH2AURKB
SCHEMBL1354262 0.91 SYK (1.00) SYKMAPK3MAPK1KCNH2AURKB
SCHEMBL14981713 0.91 SYK (0.83) SYKMAPK3MAPK1KCNH2AURKB
SCHEMBL14975783 0.90 SYK (0.82) SYKMAPK3MAPK1KCNH2AURKB
SCHEMBL14975885 0.90 SYK (0.82) SYKMAPK3MAPK1KCNH2AURKB
SCHEMBL1355098 0.89 SYK (1.00) SYKMAPK3MAPK1KCNH2AURKB
SCHEMBL1312569 0.89 SYK (0.79) SYKMAPK3MAPK1KCNH2AURKB
SCHEMBL14975680 0.88 SYK (0.78) SYKMAPK3MAPK1KCNH2AURKB
SCHEMBL16195116 0.86 SYK (1.00) SYKMAPK3MAPK1KCNH2AURKB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
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
WO-2023178094-A2 SPLEEN TYROSINE KINASE INHIBITOR, COMPOSITION, AND METHODS OF USE PURDUE RESEARCH FOUNDATION (US) 2023-09-21 — — WO claimed
EP-3191098-A1 COMBINATIONS AND DOSING REGIMES TO TREAT RB-POSITIVE TUMORS G1 Therapeutics, Inc. (US) 2017-07-19 — — EP claimed
WO-2016040858-A1 COMBINATIONS AND DOSING REGIMES TO TREAT RB-POSITIVE TUMORS G1 THERAPEUTICS, INC. (US) 2016-03-17 — — WO claimed
EP-2376481-B1 PYRIMIDINECARBOXAMIDE DERIVATIVES AS INHIBITORS OF SYK KINASE GLAXO GROUP LTD (GB) 2013-08-07 — — EP claimed
EP-2376481-A1 PYRIMIDINECARBOXAMIDE DERIVATIVES AS INHIBITORS OF SYK KINASE Glaxo Group Limited (GB) 2011-10-19 — — EP claimed
WO-2010097248-A1 PYRIMIDINECARBOXAMIDE DERIVATIVES AS INHIBITORS OF SYK KINASE GLAXO GROUP LIMITED (GB) 2010-09-02 — — WO claimed
CN-122059926-A Heterocyclic degradation determinants for target protein degradation C4医药公司 2026-05-19 — — CN disclosed
EP-4735438-A2 HETEROBIFUNCTIONAL COMPOUNDS FOR THE DEGRADATION OF KRAS Merck Patent GmbH (DE) 2026-05-06 — — EP disclosed
EP-4735452-A2 HETEROBIFUNCTIONAL COMPOUNDS FOR THE DEGRADATION OF KRAS PROTEIN Merck Patent GmbH (DE) 2026-05-06 — — EP disclosed
US-12605450-B2 C3-carbon linked glutarimide Degronimers for target protein degradation C4 THERAPEUTICS, INC. (US) 2026-04-21 — — US disclosed
US-20110275655-A1 PYRIMIDINECARBOXAMIDE DERIVATIVES AS INHIBITORS OF SYK KINASE GLAXO GROUP LIMITED (GB) 2011-11-10 — — US disclosed
US-20110275655-A1 PYRIMIDINECARBOXAMIDE DERIVATIVES AS INHIBITORS OF SYK KINASE GLAXO GROUP LIMITED (GB) 2011-11-10 — — US disclosed
EP-2376481-A1 PYRIMIDINECARBOXAMIDE DERIVATIVES AS INHIBITORS OF SYK KINASE Glaxo Group Limited (GB) 2011-10-19 — — EP disclosed
WO-2010097248-A1 PYRIMIDINECARBOXAMIDE DERIVATIVES AS INHIBITORS OF SYK KINASE GLAXO GROUP LIMITED (GB) 2010-09-02 — — WO disclosed
WO-2010097248-A1 PYRIMIDINECARBOXAMIDE DERIVATIVES AS INHIBITORS OF SYK KINASE GLAXO GROUP LIMITED (GB) 2010-09-02 — — 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-12605450-B2 C3-carbon linked glutarimide Degronimers for target protein degradation NEDD4, UBE3A, UBE3C SYK 4313/4885MAPK3 3406/4885MAPK1 4256/4885
US-20250186432-A1 SPLEEN TYROSINE KINASE INHIBITOR, COMPOSITION, AND METHODS OF USE SYK, BTK, G6PD SYK 1/4885MAPK3 285/4885MAPK1 873/4885
US-20110275655-A1 PYRIMIDINECARBOXAMIDE DERIVATIVES AS INHIBITORS OF SYK KINASE SYK, KIT, LCK SYK 1/4885MAPK3 770/4885MAPK1 487/4885

“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.

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