SCHEMBL415994

SCHEMBL415994

COC(=O)c1cnc2[nH]ccc2c1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CDK8 P49336 6/20 0.68
KDR P35968 3/20 0.52
CDK7 P50613 2/20 0.52
PLK4 O00444 1/20 0.52
DCLK1 O15075 1/20 0.52
ROCK2 O75116 1/20 0.52
PRKD3 O94806 1/20 0.52
MAP4K4 O95819 1/20 0.52
PAK4 O96013 1/20 0.52
CHEK2 O96017 1/20 0.52
INSR P06213 1/20 0.52
CDK1 P06493 1/20 0.52
FES P07332 1/20 0.52
ROS1 P08922 1/20 0.52
PDGFRB P09619 1/20 0.52
PDGFRA P16234 1/20 0.52
FER P16591 1/20 0.52
CDK2 P24941 1/20 0.52
MARK3 P27448 1/20 0.52
LTK P29376 1/20 0.52

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 SCHEMBL14688124 0.98 CDK8 (0.67) CDK8KDRCDK7PLK4DCLK1
SCHEMBL28261817 0.86 CDK8 (0.52) CDK8KDRCDK7PLK4DCLK1
SCHEMBL28188182 0.85 CDK8 (0.52) CDK8KDRCDK7PLK4DCLK1
SCHEMBL298121 0.85 CDK8 (0.52) CDK8KDRCDK7PLK4DCLK1
SCHEMBL12410716 0.83 CDK8 (0.67) CDK8KDRCDK7PLK4DCLK1
SCHEMBL27732330 0.83 RIPK1 (0.56) CDK8KDRCDK7PLK4DCLK1
SCHEMBL27726566 0.83 CDK8 (0.50) CDK8KDRCDK7PLK4DCLK1
SCHEMBL298264 0.81 RIPK1 (0.55) CDK8KDRCDK7PLK4DCLK1
SCHEMBL27890826 0.81 CDK8 (0.48) CDK8KDRCDK7PLK4DCLK1
SCHEMBL298301 0.81 CDK8 (0.68) CDK8KDRCDK7PLK4DCLK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103864780-A Preparation of new drug 1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl ester derivatives and application in antitumor drugs UNIV TIANJIN SCIENCE & TECH 2014-06-18 CN claimed
US-12428411-B2 Preparation of oxindole derivatives as novel diacylglyceride o-acyltransferase 2 inhibitors MERCK SHARP & DOHME LLC (US) 2025-09-30 US disclosed
US-12410159-B2 Preparation of oxindole derivatives as novel diacylglyceride O-acyltransferase 2 inhibitors MERCK SHARP & DOHME LLC (US) 2025-09-09 US disclosed
WO-2025129167-A1 INHIBITORS OF THE SURFACE EXPRESSION OF THE VOLTAGE-GATED SODIUM ION CHANNEL 1.7 (NAV1.7) AND THEIR THERAPEUTIC USES THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPT. OF HEALTH AND HUMAN SERVICES (US) 2025-06-19 WO disclosed
WO-2025101738-A1 BRM TARGETING COMPOUNDS AND ASSOCIATED METHODS OF USE PRELUDE THERAPEUTICS INCORPORATED (US) 2025-05-15 WO disclosed
WO-2025076284-A1 COMPOUNDS, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME DELPHIA THERAPEUTICS, INC. (US) 2025-04-10 WO disclosed
CN-115335043-B PGDH inhibitors and methods of making and using the same 迈欧伏特治疗公司 2025-03-28 CN disclosed
US-12252490-B2 Inhibiting deubiquitinase USP25 and USP28 VALO HEALTH, INC. (US) 2025-03-18 US disclosed
CN-119490502-A Aromatic heterocyclic pyrrolidones and uses thereof 杭州百新生物医药科技有限公司 2025-02-21 CN disclosed
WO-2024254599-A1 HPGD INHIBITORS AND USES THEREOF NIMBUS DISCOVERY, INC. (US) 2024-12-12 WO disclosed
EP-1893612-A1 PYRROLO [2, 3-B]PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON, INC. (US) 2008-03-05 EP disclosed
WO-2008005457-A2 PYRIDINONYL PDK1 INHIBITORS SUNESIS PHARMACEUTICALS (US) 2008-01-10 WO disclosed
EP-1664043-B1 COMPOSITIONS USEFUL AS INHIBITORS OF PROTEIN KINASES VERTEX PHARMA (US) 2007-11-14 EP disclosed
EP-1664043-B1 COMPOSITIONS USEFUL AS INHIBITORS OF PROTEIN KINASES VERTEX PHARMA (US) 2007-11-14 EP disclosed
WO-2007002325-A1 PYRROLO[2,3-B] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON, INC. (US) 2007-01-04 WO disclosed
WO-2007002325-A1 PYRROLO[2,3-B] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON, INC. (US) 2007-01-04 WO disclosed
WO-2007002433-A1 PYRROLO [2, 3-B] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON, INC. (US) 2007-01-04 WO disclosed
WO-2007002433-A1 PYRROLO [2, 3-B] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON, INC. (US) 2007-01-04 WO disclosed
US-20050137201-A1 Compositions useful as inhibitors of protein kinases VERTEX PHARMACEUTICALS INCORPORATED 2005-06-23 US disclosed
WO-2005028475-A2 COMPOSITIONS USEFUL AS INHIBITORS OF PROTEIN KINASES VERTEX PHARMACEUTICALS INCORPORATED (US) 2005-03-31 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 (4 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-12410159-B2 Preparation of oxindole derivatives as novel diacylglyceride O-acyltransferase 2 inhibitors DGAT2, DGAT1, MOGAT2 CDK8 2547/4885KDR 2422/4885CDK7 1673/4885
US-12428411-B2 Preparation of oxindole derivatives as novel diacylglyceride o-acyltransferase 2 inhibitors DGAT2, DGAT1, MOGAT2 CDK8 2547/4885KDR 2422/4885CDK7 1673/4885
US-12252490-B2 Inhibiting deubiquitinase USP25 and USP28 USP28, USP25, USP30 CDK8 227/4885KDR 4632/4885CDK7 644/4885
US-20050137201-A1 Compositions useful as inhibitors of protein kinases MAP3K20, PACSIN2, MAP3K6 CDK8 273/4885KDR 2229/4885CDK7 255/4885

“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.