Seliciclib

Seliciclib

SCHEMBL94728

CC[C@H](CO)Nc1nc(NCc2ccccc2)c2ncn(C(C)C)c2n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CDK1CDK2CDK5CDK7CDK9

The experimentally established mechanism targets of Seliciclib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CDK1 known ✓ P06493 14/20 1.00
CDK5 known ✓ Q00535 10/20 1.00
CDK2 known ✓ P24941 9/20 1.00
CDK7 known ✓ P50613 6/20 1.00
CDK9 known ✓ P50750 5/20 1.00
CCNE1 P24864 7/20 1.00
CCNB1 P14635 6/20 1.00
CCNK O75909 6/20 1.00
CDK12 Q9NYV4 6/20 1.00
CCNA2 P20248 4/20 1.00
CDK4 P11802 4/20 1.00
CCND1 P24385 4/20 1.00
CCNH P51946 4/20 1.00
DYRK1A Q13627 3/20 1.00
CCNA1 P78396 3/20 1.00
CCNB2 O95067 3/20 1.00
MAPK1 P28482 3/20 1.00
CCNB3 Q8WWL7 3/20 1.00
CSNK1D P48730 2/20 1.00
CLK2 P49760 2/20 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
(Rs)-Roscovitine SCHEMBL172593 1.00 CDK1 (1.00) CDK1CDK5CDK2CCNE1CDK7
(S)-Roscovitine SCHEMBL29415376 1.00 CDK1 (1.00) CDK1CDK5CDK2CCNE1CDK7
(S)-Roscovitine SCHEMBL2907488 1.00 CDK1 (1.00) CDK1CDK5CDK2CCNE1CDK7
(Rs)-Roscovitine SCHEMBL15163619 1.00 CDK1 (1.00) CDK1CDK5CDK2CCNE1CDK7
SCHEMBL17628573 0.94 CDK2 (1.00) CDK1CDK5CDK2CCNE1CDK7
SCHEMBL13001898 0.94 CDK2 (1.00) CDK1CDK5CDK2CCNE1CDK7
SCHEMBL14403894 0.94 CDK1 (0.88) CDK1CDK5CDK2CCNE1CDK7
SCHEMBL1213597 0.92 CDK1 (1.00) CDK1CDK5CDK2CCNE1CDK7
SCHEMBL2098199 0.92 CDK1 (1.00) CDK1CDK5CDK2CCNE1CDK7
SCHEMBL23198590 0.92 CDK1 (0.85) CDK1CDK5CDK2CCNE1CDK7

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

Appears in 4085 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3841097-B1 2,6-BIS(((1H-BENZO[D]IMIDAZOL-2-YL)THIO)METHYL)PYRIDINE AND N2,N6-DIBENZYLPYRIDINE-2,6-DICARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE (PI3K) INHIBITORS FOR TREATING CANCER BIOMEDICAL RES FOUNDATION OF THE ACADEMY OF ATHENS BRFAA (GR) 2026-05-20 EP claimed
WO-2025217307-A9 METHODS FOR PREDICTING RESPONSE TO A RAS(ON) INHIBITOR AND COMBINATION THERAPIES Revolution Medicines, Inc. (US) 2026-05-15 WO claimed
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS HANGZHOU DAC BIOTECH CO., LTD. (CN) 2026-04-23 US claimed
US-20260085061-A1 PHTHALAZINE DERIVATIVES AS PYRUVATE KINASE MODULATORS SITRYX THERAPEUTICS LIMITED (GB) 2026-03-26 US claimed
US-20260076952-A1 Agent for Treatment of Neutropenia UNIV TUEBINGEN MEDIZINISCHE FAKULTAET (DE) 2026-03-19 US claimed
US-12576124-B2 Formulation of a conjugate of a tubulysin analog to a cell-binding molecule HANGZHOU DAC BIOTECH CO., LTD (CN) 2026-03-17 US claimed
US-12577255-B2 MDM2-based modulators of proteolysis and associated methods of use ARVINAS OPERATIONS, INC. (US) 2026-03-17 US claimed
EP-4704832-A2 BIFUNCTIONAL SMALL MOLECULES TO TARGET THE SELECTIVE DEGRADATION OF CIRCULATING PROTEINS Biohaven Therapeutics Ltd. (VG) 2026-03-11 EP claimed
US-12558308-B2 Drug-loaded biodegradable microbead compositions including drug-containing vesicular agents C.R. BARD, INC. (US) 2026-02-24 US claimed
EP-4695235-A1 NOVEL GSPT1 DEGRADER AND USE THEREOF Cyrus Therapeutics Inc. (KR) 2026-02-18 EP claimed
EP-2562265-A1 Susceptibility to selective CDK9 inhibitors Lead Discovery Center GmbH (DE) 2013-02-27 EP claimed
EP-2561867-A1 CDK9 inhibitors in the treatment of midline carcinoma Lead Discovery Center GmbH (DE) 2013-02-27 EP claimed
US-20070275986-A1 Use of purine derivatives for the production of medicaments for the treatment of mucoviscidosis and diseases related to protein addressing errors in cells CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2007-11-29 US claimed
EP-1841401-A1 REDUCTION OF HAIR GROWTH WITH SURVIVIN INHIBITORS The Gillette Company (US) 2007-10-10 EP claimed
WO-2006069192-A1 REDUCTION OF HAIR GROWTH WITH SURVIVIN INHIBITORS THE GILLETTE COMPANY (US) 2006-06-29 WO claimed
US-20060135461-A1 Reduction of hair growth GILLETTE COMPANY, THE 2006-06-22 US claimed
US-20030186999-A1 Purine derivatives having, in particular, antiproliferative properties, and their biological uses CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIGUE (C.N.R.S.) 2003-10-02 US claimed
US-20030069430-A1 Substituted oxindole derivatives as protein tyrosine and as protein serine/threonine kinase inhibitors and compositions and methods of treating chemotherapy and radiation therapy side effects SMITHKLINE BEECHAM CORPORATION 2003-04-10 US claimed
EP-0874847-B1 NOVEL PURINE DERIVATIVES HAVING, IN PARTICULAR, ANTIPROLIFERATIVE PROPERTIES, AND BIOLOGICAL USES THEREOF CENTRE NAT RECH SCIENT (FR) 2003-03-19 EP claimed
US-20020049218-A1 Purine derivatives having, in particular, antiproliferative properties, and their biological uses CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIGUE (C.N.R.S.) 2002-04-25 US claimed