SCHEMBL298150

SCHEMBL298150

N#Cc1cnc2[nH]ccc2c1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RIPK1 Q13546 4/20 0.69
CDK8 P49336 6/20 0.50
AXL P30530 3/20 0.50
IMPDH2 P12268 1/20 0.50
IMPDH1 P20839 1/20 0.50
PIK3CD O00329 2/20 0.49
PIK3CA P42336 2/20 0.49
PIK3CB P42338 1/20 0.49
PIK3CG P48736 1/20 0.49
NUDT1 P36639 2/20 0.44
MTOR P42345 1/20 0.42
KDR P35968 3/20 0.42
FGFR1 P11362 2/20 0.42
PLK4 O00444 2/20 0.42
ROCK2 O75116 2/20 0.42
PRKD3 O94806 2/20 0.42
MAP4K4 O95819 2/20 0.42
INSR P06213 2/20 0.42
CDK1 P06493 2/20 0.42
ROS1 P08922 2/20 0.42

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
SCHEMBL28081590 0.89 AXL (0.62) RIPK1CDK8AXLIMPDH2IMPDH1
SCHEMBL30569001 0.82 RIPK1 (0.49) RIPK1CDK8AXLIMPDH2IMPDH1
SCHEMBL31065011 0.82 RIPK1 (1.00) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL2013329 0.81 RIPK1 (0.51) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL293195 0.81 RIPK1 (0.51) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL17761629 0.79 RIPK1 (0.49) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL1329244 0.77 CDK8 (0.58) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL1484205 0.76 RIPK1 (0.64) RIPK1CDK8AXLIMPDH2IMPDH1
SCHEMBL297592 0.76 RIPK1 (0.47) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL29543783 0.76 RIPK1 (0.47) RIPK1CDK8AXLPIK3CDPIK3CA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3445762-B1 SUBSTITUTED BICYCLIC HETEROCYCLIC COMPOUNDS BRISTOL MYERS SQUIBB CO (US) 2023-09-13 EP claimed
CN-109311874-A The bicyclic heterocyclic compounds being substituted 百时美施贵宝公司 2019-02-05 CN claimed
EP-3313840-A1 HETEROARYL SUBSTITUTED AMINOPYRIDINE COMPOUNDS Bristol-Myers Squibb Company (US) 2018-05-02 EP claimed
WO-2016210034-A1 HETEROARYL SUBSTITUTED AMINOPYRIDINE COMPOUNDS BRISTOL-MYERS SQUIBB COMPANY (US) 2016-12-29 WO claimed
EP-2970278-A1 PYRROLO[2,3-B]PYRIDINE CDK9 KINASE INHIBITORS AbbVie Inc. (US) 2016-01-20 EP claimed
WO-2014139328-A1 PYRROLO[2,3-B]PYRIDINE CDK9 KINASE INHIBITORS ABBVIE INC. (US) 2014-09-18 WO claimed
EP-2496086-A1 COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR Plexxikon, Inc. (US) 2012-09-12 EP claimed
WO-2011057022-A1 COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR PLEXXIKON, INC. (US) 2011-05-12 WO claimed
EP-2250170-A1 AZAINDOLE COMPOUNDS FOR TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS Merck Patent GmbH (DE) 2010-11-17 EP claimed
WO-2009112139-A1 AZAINDOLE COMPOUNDS FOR TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS MERCK PATENT GMBH, (DE) 2009-09-17 WO claimed
US-20090215771-A1 JNK INHIBITORS GRACZYK PIOTR 2009-08-27 US claimed
WO-2008064265-A2 COMPOUNDS MODULATING C-FMS AND/OR C-KIT ACTIVITY AND USES THEREFOR PLEXXIKON, INC. (US) 2008-05-29 WO claimed
WO-2008063888-A2 COMPOUNDS MODULATING C-FMS AND/OR C-KIT ACTIVITY AND USES THEREFOR PLEXXIKON, INC. (US) 2008-05-29 WO claimed
US-20060270646-A1 Jnk inhibitors EISAI CO., LTD. (JP) 2006-11-30 US claimed
US-20260042747-A1 KIT INHIBITORS, COMPOUNDS, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE THEREOF ALIVEXIS, INC. (JP) 2026-02-12 US disclosed
US-20250376443-A1 MASP-2 INHIBITORS AND METHODS OF USE OMEROS CORPORATION (US) 2025-12-11 US disclosed
US-20250375526-A1 IRAK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2025-12-11 US disclosed
WO-2005062795-A2 COMPOUNDS AND METHODS FOR DEVELOPMENT OF RET MODULATORS PLEXXIKON, INC. (US) 2005-07-14 WO disclosed
WO-2004078756-A2 JNK INHIBITORS EISAI CO., LTD. (JP) 2004-09-16 WO disclosed
WO-2004078756-A2 JNK INHIBITORS EISAI CO., LTD. (JP) 2004-09-16 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 (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-20250375526-A1 IRAK DEGRADERS AND USES THEREOF IRAK2, IRAK3, IRAK1 RIPK1 62/4885CDK8 646/4885AXL 356/4885
US-20250376443-A1 MASP-2 INHIBITORS AND METHODS OF USE MASP2, METAP2, SPINT2 RIPK1 2007/4885CDK8 1873/4885AXL 3473/4885
US-20060270646-A1 Jnk inhibitors MAPKAPK2, MAPK1, MAPKAPK3 RIPK1 143/4885CDK8 362/4885AXL 3946/4885
US-20090215771-A1 JNK INHIBITORS MAPKAPK2, MAPK1, MAPKAPK3 RIPK1 152/4885CDK8 360/4885AXL 3999/4885
US-20260042747-A1 KIT INHIBITORS, COMPOUNDS, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE THEREOF KIT, LTK, HRH3 RIPK1 1259/4885CDK8 257/4885AXL 1045/4885

“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.