Bi-2536

Bi-2536

SCHEMBL372489

CC[C@@H]1C(=O)N(C)c2cnc(Nc3ccc(C(=O)NC4CCN(C)CC4)cc3OC)nc2N1C1CCCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PLK1

The experimentally established mechanism targets of Bi-2536. 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
PLK1 known ✓ P53350 12/20 1.00
BRD4 O60885 15/20 1.00
PLK3 Q9H4B4 6/20 1.00
ALK Q9UM73 5/20 1.00
TAF1 P21675 5/20 1.00
PLK2 Q9NYY3 4/20 1.00
PRKD3 O94806 3/20 1.00
CLK2 P49760 3/20 1.00
PTK2 Q05397 3/20 1.00
CAMK2G Q13555 3/20 1.00
CAMK2D Q13557 3/20 1.00
PRKD2 Q9BZL6 3/20 1.00
CSNK1G1 Q9HCP0 3/20 1.00
CSNK1G3 Q9Y6M4 3/20 1.00
BRDT Q58F21 3/20 1.00
DAPK3 O43293 2/20 1.00
CHEK2 O96017 2/20 1.00
EGFR P00533 2/20 1.00
FES P07332 2/20 1.00
PHKG2 P15735 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
Bi-2536 SCHEMBL29395966 1.00 BRD4 (1.00) BRD4PLK1PLK3ALKTAF1
Bi-2536 SCHEMBL614114 1.00 BRD4 (1.00) BRD4PLK1PLK3ALKTAF1
Bi-2536 SCHEMBL16984416 1.00 BRD4 (1.00) BRD4PLK1PLK3ALKTAF1
Bi-2536 SCHEMBL29644993 0.99 BRD4 (0.99) BRD4PLK1PLK3ALKTAF1
SCHEMBL13227794 0.96 BRD4 (0.92) BRD4PLK1PLK3ALKTAF1
SCHEMBL24851804 0.96 PLK1 (1.00) BRD4PLK1PLK3ALKTAF1
SCHEMBL4515444 0.95 BRD4 (1.00) BRD4PLK1PLK3ALKTAF1
SCHEMBL16972068 0.94 BRD4 (1.00) BRD4PLK1PLK3ALKTAF1
SCHEMBL16972069 0.94 BRD4 (1.00) BRD4PLK1PLK3ALKTAF1
SCHEMBL376236 0.94 PLK1 (0.89) BRD4PLK1PLK3ALKTAF1

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 1058 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12630532-B2 Indole-substituted quinolines and their combination with Plk1 inhibitors for the treatment of cancer UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2026-05-19 US claimed
CN-122005814-A Drug-loaded polymer micelle, gel drug system, preparation method and application 苏州大学 2026-05-12 CN claimed
US-20260092327-A1 METHODS OF MONITORING MUTATIONS IN TREATMENT OF COLORECTAL CANCER CARDIFF ONCOLOGY INC (US) 2026-04-02 US claimed
US-20260076970-A1 CANCER TREATMENT USING MTDP INHIBITORS AND PLK1 INHIBITORS CARDIFF ONCOLOGY INC (US) 2026-03-19 US claimed
EP-4048260-B1 COMBINATION OF SUBSTITUTED 4-AMINOISOINDOLINE-1,3-DIONE COMPOUNDS AND SECOND ACTIVE AGENTS FOR USE IN TREATING A HEMATOLOGICAL MALIGNANCY CELGENE CORP (US) 2026-03-11 EP claimed
US-20250352551-A1 SUBSTITUTED 4-AMINOISOINDOLINE-1,3-DIONE COMPOUNDS AND SECOND ACTIVE AGENTS FOR COMBINED USE CELGENE CORPORATION 2025-11-20 US claimed
WO-2025240673-A1 CANCER TREATMENT USING AKT INHIBITORS AND PLK1 INHIBITORS CARDIFF ONCOLOGY, INC. (US) 2025-11-20 WO claimed
US-12396995-B2 Substituted 4-aminoisoindoline-1,3-dione compounds and second active agents for combined use CELGENE CORPORATION (US) 2025-08-26 US claimed
EP-4583983-A1 PLK1 INHIBITOR IN COMBINATION WITH ANTI-ANGIOGENICS FOR TREATING METASTATIC CANCER Cardiff Oncology, Inc. (US) 2025-07-16 EP claimed
EP-4583982-A1 CANCER TREATMENT USING MTDP INHIBITORS AND PLK1 INHIBITORS Cardiff Oncology, Inc. (US) 2025-07-16 EP claimed
WO-2022087371-A1 NOVEL BICYCLIC COMPOUNDS SPECTRUM PHARMACEUTICALS, INC. (US) 2022-04-28 WO claimed
WO-2022087375-A1 NOVEL HETEROCYCLIC COMPOUNDS SPECTRUM PHARMACEUTICALS, INC. (US) 2022-04-28 WO claimed
US-20220127682-A1 SELECTION AND TREATMENT OF CANCER WITH COMBINATION THERAPIES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2022-04-28 US claimed
US-20220110941-A1 COMBINATIONS FOR THE TREATMENT OF NEOPLASMS USING QUIESCENT CELL TARGETING AND INHIBITORS OF MITOSIS FELICITEX THERAPEUTICS, INC. 2022-04-14 US claimed
EP-3976195-A1 METHODS FOR TREATING SMALL CELL NEUROENDOCRINE AND RELATED CANCERS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2022-04-06 EP claimed
WO-2022055721-A1 SELECTION AND TREATMENT OF CANCER WITH COMBINATION THERAPIES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2022-03-17 WO claimed
CN-114096280-A Therapeutic constructs for co-delivery of mitotic kinase inhibitors and immune checkpoint inhibitors 俄勒冈健康与科学大学 2022-02-25 CN claimed
EP-3946313-A1 PLK1 INHIBITORS AND PSA LEVELS IN PROSTATE CANCER Cardiff Oncology, Inc. (US) 2022-02-09 EP claimed
US-20180369214-A1 Methods of Diagnosing and Treating Small Cell Lung Cancer Using Polo-Like Kinase 1 (PLK1) Inhibitors EMORY UNIVERSITY 2018-12-27 US claimed
US-20080300206-A1 Alpha-Synuclein Kinase ELAN PHARMACEUTICALS, INC. (US) 2008-12-04 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (8 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-20260076970-A1 CANCER TREATMENT USING MTDP INHIBITORS AND PLK1 INHIBITORS PLK1, PLK4, PLK2 PLK1 1/4885BRD4 660/4885PLK3 7/4885
US-20250352551-A1 SUBSTITUTED 4-AMINOISOINDOLINE-1,3-DIONE COMPOUNDS AND SECOND ACTIVE AGENTS FOR COMBINED USE DOT1L, CARM1, EZH2 PLK1 19/4885BRD4 13/4885PLK3 501/4885
US-12396995-B2 Substituted 4-aminoisoindoline-1,3-dione compounds and second active agents for combined use DOT1L, CARM1, EZH2 PLK1 19/4885BRD4 13/4885PLK3 501/4885
US-20080300206-A1 Alpha-Synuclein Kinase SNCA, PLK2, LMTK2 PLK1 24/4885BRD4 1493/4885PLK3 6/4885
US-20220127682-A1 SELECTION AND TREATMENT OF CANCER WITH COMBINATION THERAPIES PLK4, PLK2, BUB1B PLK1 5/4885BRD4 1076/4885PLK3 4/4885
US-20220110941-A1 COMBINATIONS FOR THE TREATMENT OF NEOPLASMS USING QUIESCENT CELL TARGETING AND INHIBITORS OF MITOSIS BUB1B, BUB1, CCNB1 PLK1 5/4885BRD4 316/4885PLK3 370/4885
US-20260092327-A1 METHODS OF MONITORING MUTATIONS IN TREATMENT OF COLORECTAL CANCER KRAS, HRAS, NRAS PLK1 25/4885BRD4 1886/4885PLK3 103/4885
US-12630532-B2 Indole-substituted quinolines and their combination with Plk1 inhibitors for the treatment of cancer PLK1, MYC, PLK4 PLK1 1/4885BRD4 118/4885PLK3 10/4885

“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.