SCHEMBL10098691

SCHEMBL10098691

CN1C(=O)c2ccccc2N(C)c2nc(Cl)ncc21

nearest known ligand 0.56

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ MAPK7 Q13164 11/20 0.56
▸ DCLK1 O15075 10/20 0.55
▸ LRRK2 Q5S007 11/20 0.54
▸ PIK3CD O00329 3/20 0.54
▸ AURKA O14965 3/20 0.54
▸ PIK3C2G O75747 3/20 0.54
▸ PIK3CG P48736 3/20 0.54
▸ AURKB Q96GD4 3/20 0.54
▸ NUAK1 O60285 2/20 0.47
▸ TTR P02766 1/20 0.46
▸ CES1 P23141 1/20 0.46
▸ BRD4 O60885 3/20 0.46
▸ GAK O14976 1/20 0.45
▸ TNK2 Q07912 1/20 0.45
▸ TNK1 Q13470 1/20 0.45
▸ DCLK2 Q8N568 1/20 0.45
▸ BRDT Q58F21 1/20 0.45

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
SCHEMBL20094145 0.85 LRRK2 (0.50) MAPK7DCLK1LRRK2PIK3CDAURKA
SCHEMBL20094162 0.85 MAPK7 (0.51) MAPK7DCLK1LRRK2PIK3CDAURKA
SCHEMBL25357908 0.84 DCLK1 (0.52) MAPK7DCLK1LRRK2PIK3CDAURKA
SCHEMBL30526068 0.84 DCLK1 (0.52) MAPK7DCLK1LRRK2PIK3CDAURKA
SCHEMBL17721092 0.84 MAPK7 (0.57) MAPK7DCLK1LRRK2PIK3CDAURKA
SCHEMBL10098766 0.83 DCLK1 (0.58) MAPK7DCLK1LRRK2PIK3CDAURKA
SCHEMBL19457452 0.82 PIK3CD (0.56) MAPK7LRRK2PIK3CDAURKAPIK3C2G
SCHEMBL30131807 0.82 PIK3CD (0.56) MAPK7LRRK2PIK3CDAURKAPIK3C2G
SCHEMBL16065726 0.81 MAPK7 (0.54) MAPK7DCLK1LRRK2PIK3CDAURKA
SCHEMBL20094197 0.81 DCLK1 (0.53) MAPK7DCLK1LRRK2PIK3CDAURKA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116375713-B DCLK1 protein degradation targeting chimeric and application thereof 中国人民解放军海军军医大学 2024-11-19 — — CN disclosed
EP-3528814-B1 PYRIMIDO-DIAZEPINONE KINASE SCAFFOLD COMPOUNDS AND METHODS OF TREATING DCLK1/2-MEDIATED DISORDERS DANA FARBER CANCER INST INC (US) 2024-08-14 — — EP disclosed
US-12023385-B2 Tunable endogenous protein degradation with heterobifunctional compounds DANA-FARBER CANCER INSTITUTE, INC. (US) 2024-07-02 — — US disclosed
US-12023385-B2 Tunable endogenous protein degradation with heterobifunctional compounds DANA-FARBER CANCER INSTITUTE, INC. (US) 2024-07-02 — — US disclosed
US-20240124460-A1 METHODS AND COMPOSITIONS FOR TARGETED PROTEIN DEGRADATION RANOK THERAPEUTICS (HANGZHOU) CO. LTD. (CN) 2024-04-18 — — US disclosed
CN-114478539-B Novel DCLK1 inhibitor and preparation method and application thereof 中国人民解放军海军军医大学 2024-02-02 — — CN disclosed
EP-4229061-A1 METHODS AND COMPOSITIONS FOR TARGETED PROTEIN DEGRADATION Ranok Therapeutics (Hangzhou) Co. Ltd. (CN) 2023-08-23 — — EP disclosed
EP-3256470-B1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA FARBER CANCER INST INC (US) 2023-07-26 — — EP disclosed
CN-116375713-A DCLK1 protein degradation targeting chimeric and application thereof 中国人民解放军海军军医大学 2023-07-04 — — CN disclosed
US-11583586-B2 Methods to induce targeted protein degradation through bifunctional molecules DANA-FARBER CANCER INSTITUTE, INC. (US) 2023-02-21 — — US disclosed
US-20160176916-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2016-06-23 — — US disclosed
US-20160122357-A1 PYRIMIDO-DIAZEPINONE KINASE SCAFFOLD COMPOUNDS AND METHODS OF TREATING DISORDERS DANA-FARBER CANCER INSTITUTE, INC. 2016-05-05 — — US disclosed
US-20160122357-A1 PYRIMIDO-DIAZEPINONE KINASE SCAFFOLD COMPOUNDS AND METHODS OF TREATING DISORDERS DANA-FARBER CANCER INSTITUTE, INC. 2016-05-05 — — US disclosed
US-9266890-B2 Pyrimido-diazepinone kinase scaffold compounds and methods of treating disorders DANA-FARBER CANCER INSTITUTE, INC. (US) 2016-02-23 — — US disclosed
US-9266890-B2 Pyrimido-diazepinone kinase scaffold compounds and methods of treating disorders DANA-FARBER CANCER INSTITUTE, INC. (US) 2016-02-23 — — US disclosed
WO-2016022902-A1 DIAZEPANE DERIVATIVES AND USES THEREOF DANA-FARBER CANCER INSTITUTE, INC. (US) 2016-02-11 — — WO disclosed
WO-2014160430-A1 SMALL MOLECULE LRRK2 AND ERK5 INHIBITORS GEORGETOWN UNIVERSITY (US) 2014-10-02 — — WO disclosed
US-20120040961-A1 PYRIMIDO-DIAZEPINONE KINASE SCAFFOLD COMPOUNDS AND METHODS OF TREATING DISORDERS DANA-FARBER CANCER INSTITUTE (US) 2012-02-16 — — US disclosed
US-20120040961-A1 PYRIMIDO-DIAZEPINONE KINASE SCAFFOLD COMPOUNDS AND METHODS OF TREATING DISORDERS DANA-FARBER CANCER INSTITUTE (US) 2012-02-16 — — US disclosed
WO-2010080712-A2 PYRIMIDO-DIAZEPINONE KINASE SCAFFOLD COMPOUNDS AND METHODS OF TREATING DISORDERS DANA FARBER CANCER INSTITUTE (US) 2010-07-15 — — 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 (6 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-20120040961-A1 PYRIMIDO-DIAZEPINONE KINASE SCAFFOLD COMPOUNDS AND METHODS OF TREATING DISORDERS BRSK2, BRSK1, TAOK3 MAPK7 263/4885DCLK1 480/4885LRRK2 364/4885
US-11583586-B2 Methods to induce targeted protein degradation through bifunctional molecules CRBN, MDM2, MYCBP MAPK7 3496/4885DCLK1 1829/4885LRRK2 1253/4885
US-20160122357-A1 PYRIMIDO-DIAZEPINONE KINASE SCAFFOLD COMPOUNDS AND METHODS OF TREATING DISORDERS BRSK2, STK3, BRSK1 MAPK7 253/4885DCLK1 453/4885LRRK2 340/4885
US-12023385-B2 Tunable endogenous protein degradation with heterobifunctional compounds DBN1, MYCBP, PSMG3 MAPK7 4605/4885DCLK1 2364/4885LRRK2 1995/4885
US-20240124460-A1 METHODS AND COMPOSITIONS FOR TARGETED PROTEIN DEGRADATION PSMG3, PSMC2, PSMA6 MAPK7 1599/4885DCLK1 2928/4885LRRK2 1277/4885
US-20160176916-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP MAPK7 3496/4885DCLK1 1829/4885LRRK2 1253/4885

“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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