Alvocidib

Alvocidib

SCHEMBL3652

CN1CC[C@H](c2c(O)cc(O)c3c(=O)cc(-c4ccccc4Cl)oc23)[C@H](O)C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CDK1CDK2CDK4CDK6CDK7CDK9

The experimentally established mechanism targets of Alvocidib. 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
CDK2 known ✓ P24941 14/20 1.00
CDK4 known ✓ P11802 12/20 1.00
CDK1 known ✓ P06493 11/20 1.00
CDK9 known ✓ P50750 10/20 1.00
CDK7 known ✓ P50613 3/20 1.00
CDK6 known ✓ Q00534 2/20 1.00
CCND1 P24385 11/20 1.00
CCNB1 P14635 9/20 1.00
CCNT1 O60563 9/20 1.00
CCNA2 P20248 8/20 1.00
CCNB2 O95067 6/20 1.00
CCNB3 Q8WWL7 6/20 1.00
CCNE1 P24864 6/20 1.00
GSK3A P49840 4/20 1.00
CCNE2 O96020 4/20 1.00
GSK3B P49841 3/20 1.00
CCNA1 P78396 3/20 1.00
PLK4 O00444 2/20 1.00
PRKD3 O94806 2/20 1.00
EGFR P00533 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
Alvocidib SCHEMBL5868074 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9
Alvocidib SCHEMBL29351027 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9
Alvocidib SCHEMBL29577824 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9
Alvocidib SCHEMBL12445809 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9
Alvocidib SCHEMBL29388553 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9
Alvocidib SCHEMBL8214028 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9
Alvocidib SCHEMBL3651 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9
Alvocidib SCHEMBL16927354 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9
Flavopyridol SCHEMBL22580715 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9
Alvocidib SCHEMBL28199338 1.00 CDK2 (1.00) CDK2CDK4CDK1CCND1CDK9

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 26103 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260116861-A1 ISOXAZOLE HYDROXAMIC ACIDS AS HISTONE DEACETYLASE 6 INHIBITORS THE GEORGE WASHINGTON UNIVERSITY, A CONGRESSIONALLY CHARTERED NOT-FOR-PROFIT CORPORATION (US) 2026-04-30 US claimed
US-20260102468-A1 COMPOSITIONS AND METHODS FOR MARCO INHIBITION AND IMPROVED DRUG DELIVERY UNIV TEXAS (US) 2026-04-16 US claimed
EP-3515892-B1 COMPOUNDS AND METHODS FOR IDO AND TDO MODULATION, AND INDICATIONS THEREFOR PLEXXIKON INC (US) 2026-04-15 EP claimed
US-20260091119-A1 ISOLATED TARGETED DELIVERY SYSTEM FOR THE TREATMENT OF GLIOMA CELLIS AG (CH) 2026-04-02 US claimed
US-20260076952-A1 Agent for Treatment of Neutropenia UNIV TUEBINGEN MEDIZINISCHE FAKULTAET (DE) 2026-03-19 US claimed
US-12569494-B2 Compositions and methods to promote thymic regeneration FRED HUTCHINSON CANCER CENTER (US) 2026-03-10 US claimed
US-20260053750-A1 INHALABLE COMPOSITIONS OF CDK9 INHIBITORS OWEN MATTHEW (US) 2026-02-26 US claimed
EP-4683632-A1 A CYCLIN-DEPENDENT KINASE 2/4/9 INHIBITOR FOR THE TREATMENT OF NEUTROPENIA Eberhard Karls Universität Tübingen, Medizinische Fakultät (DE) 2026-01-28 EP claimed
US-20260014140-A1 DOSAGES OF IMMUNOCONJUGATES OF ANTIBODIES AND SN-38 FOR IMPROVED EFFICACY AND DECREASED TOXICITY IMMUNOMEDICS INC (US) 2026-01-15 US claimed
US-12522572-B2 Isoxazole hydroxamic acids as histone deacetylase 6 inhibitors THE GEORGE WASHINGTON UNIVERSITY, A CONGRESSIONALLY CHARTERED NOT-FOR-PROFIT CORPORATION (US) 2026-01-13 US claimed
WO-2000044362-A2 THE USE OF 4-H-1-BENZOPYRAN-4-ONE DERIVATIVES AS INHIBITORS OF SMOOTH MUSCLE CELL PROLIFERATION AVENTIS PHARMACEUTICALS INC. (US) 2000-08-03 WO claimed
US-6087366-A Use of flavopiridol or a pharmaceutically acceptable salt thereof for inhibiting cell damage or cell death THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2000-07-11 US claimed
WO-2000029427-A2 ANTENNAPEDIA HOMEODOMAIN HELIX 3 DERIVED TRANSLOCATION VECTORS CYCLACEL LIMITED (GB) 2000-05-25 WO claimed
WO-2000024885-A2 p53 MORPHOLINO-BASED ANTISENSE AVI BIOPHARMA, INC. (US) 2000-05-04 WO claimed
WO-2000001417-A1 DELIVERY SYSTEM CYCLACEL LIMITED (GB) 2000-01-13 WO claimed
WO-1999032660-A9 EXPLOITING GENOMICS IN THE SEARCH FOR NEW DRUGS AFFYMETRIX INC (US) 1999-09-23 WO claimed
WO-1999032660-A1 EXPLOITING GENOMICS IN THE SEARCH FOR NEW DRUGS AFFYMETRIX (US) 1999-07-01 WO claimed
EP-0919244-A2 Combinations for the treatment of tumours Forschungszentrum Borstel Zentrum für Medizin und Biowissenschaften (DE) 1999-06-02 EP claimed
EP-0888458-A1 COMBINATIONS OF PKC INHIBITORS AND THERAPEUTIC AGENTS FOR TREATING CANCERS Sloan-Kettering Institute For Cancer Research (US) 1999-01-07 EP claimed
WO-1997030174-A1 COMBINATIONS OF PKC INHIBITORS AND THERAPEUTIC AGENTS FOR TREATING CANCERS SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1997-08-21 WO claimed