Alvocidib

Alvocidib

SCHEMBL8214028

CN1CCC(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 SCHEMBL3652 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

Claimed or disclosed in 200 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023196943-A1 DR5 AGONIST AND PLK1 INHIBITOR OR CDK INHIBITOR COMBINATION THERAPY Inhibrx, Inc. (US) 2023-10-12 WO disclosed
US-20220220072-A1 METHOD FOR PRODUCING CIS-(-) FLOCINOPIPERIDOL Sumitomo Pharma Co., Ltd. (JP) 2022-07-14 US disclosed
EP-3527574-B1 ALVOCIDIB PRODRUGS HAVING INCREASED BIOAVAILABILITY SUMITOMO DAINIPPON PHARMA ONCOLOGY INC (US) 2022-04-06 EP disclosed
WO-2021236721-A1 METHODS FOR PREVENTING, REVERSING OR TREATING A COVID-19 INFECTION BROWN UNIVERSITY (US) 2021-11-25 WO disclosed
EP-3129371-B1 INHIBITORS OF CYCLIN-DEPENDENT KINASE 7 (CDK7) SYROS PHARMACEUTICALS INC (US) 2020-07-29 EP disclosed
US-20190134033-A1 PHARMACEUTICAL COMBINATIONS NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH, INC. 2019-05-09 US disclosed
EP-2831282-B1 PREDICTIVE BIOMARKER USEFUL FOR CANCER THERAPY MEDIATED BY A CDK INHIBITOR MERCK SHARP & DOHME (US) 2018-07-04 EP disclosed
EP-2225235-B1 THIAZOLE CARBOXAMIDE DERIVATIVES AND THEIR USE TO TREAT CANCER MERCK SHARP & DOHME (US) 2017-09-06 EP disclosed
EP-2752422-B1 Stereoselective synthesis of phosphorus containing actives GILEAD PHARMASSET LLC (US) 2017-08-16 EP disclosed
EP-2078003-B1 ANILINOPIPERAZINE DERIVATIVES AND METHODS OF USE THEREOF MERCK SHARP & DOHME (US) 2017-03-08 EP disclosed
US-20070032495-A1 Pyrazolotriazines as kinase inhibitors MERCK SHARP & DOHME LLC 2007-02-08 US disclosed
US-20070032495-A1 Pyrazolotriazines as kinase inhibitors MERCK SHARP & DOHME LLC 2007-02-08 US disclosed
US-7166602-B2 Pyrazolotriazines as kinase inhibitors SCHERING CORPORATION (US) 2007-01-23 US disclosed
US-7166602-B2 Pyrazolotriazines as kinase inhibitors SCHERING CORPORATION (US) 2007-01-23 US disclosed
US-7161003-B1 Pyrazolopyrimidines as cyclin dependent kinase inhibitors SCHERING CORPORATION (US) 2007-01-09 US disclosed
US-7161003-B1 Pyrazolopyrimidines as cyclin dependent kinase inhibitors SCHERING CORPORATION (US) 2007-01-09 US disclosed
US-20060106023-A1 Novel imidazopyrazines as cyclin dependent kinase inhibitors SCHERING CORPORATION 2006-05-18 US disclosed
US-20060106023-A1 Novel imidazopyrazines as cyclin dependent kinase inhibitors SCHERING CORPORATION 2006-05-18 US disclosed
US-20040063715-A1 Novel imidazopyrazines as cyclin dependent kinase inhibitors SCHERING CORPORATION 2004-04-01 US disclosed
US-20040063715-A1 Novel imidazopyrazines as cyclin dependent kinase inhibitors SCHERING CORPORATION 2004-04-01 US 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-20220220072-A1 METHOD FOR PRODUCING CIS-(-) FLOCINOPIPERIDOL DHFR, DHPS, TKT CDK2 1217/4885CDK4 209/4885CDK1 2289/4885
US-20040063715-A1 Novel imidazopyrazines as cyclin dependent kinase inhibitors CDK2, CDKN1A, CDK1 CDK2 1/4885CDK4 5/4885CDK1 3/4885
US-20060106023-A1 Novel imidazopyrazines as cyclin dependent kinase inhibitors CDK2, CDKN1A, CDK1 CDK2 1/4885CDK4 4/4885CDK1 3/4885
US-20070032495-A1 Pyrazolotriazines as kinase inhibitors CDK2, CDK5, CDK1 CDK2 1/4885CDK4 11/4885CDK1 3/4885
US-20190134033-A1 PHARMACEUTICAL COMBINATIONS TP53, HRAS, KRAS CDK2 266/4885CDK4 194/4885CDK1 1502/4885

“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.