Volasertib

Volasertib

SCHEMBL14136759

CCC1C(=O)N(C)c2cnc(Nc3ccc(C(=O)NC4CCC(N5CCN(CC6CC6)CC5)CC4)cc3OC)nc2N1C(C)C

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 Volasertib. 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 17/20 1.00
BRD4 O60885 12/20 1.00
PLK3 Q9H4B4 6/20 1.00
PTK2 Q05397 4/20 1.00
BRDT Q58F21 4/20 1.00
PLK2 Q9NYY3 4/20 1.00
PDXK O00764 2/20 1.00
NEK3 P51956 2/20 1.00
CAMKK2 Q96RR4 2/20 1.00
WEE1 P30291 1/20 1.00
PRKD3 O94806 3/20 0.64
CLK2 P49760 3/20 0.64
CAMK2G Q13555 3/20 0.64
CAMK2D Q13557 3/20 0.64
PRKD2 Q9BZL6 3/20 0.64
CSNK1G1 Q9HCP0 3/20 0.64
CSNK1G3 Q9Y6M4 3/20 0.64
MAP4K4 O95819 2/20 0.64
PRKCG P05129 2/20 0.64
RPS6KA3 P51812 2/20 0.64

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
Volasertib SCHEMBL2169101 1.00 PLK1 (1.00) PLK1BRD4PLK3PTK2BRDT
Volasertib SCHEMBL16984415 1.00 PLK1 (1.00) PLK1BRD4PLK3PTK2BRDT
Volasertib SCHEMBL30753526 1.00 PLK1 (1.00) PLK1BRD4PLK3PTK2BRDT
Volasertib SCHEMBL9888052 1.00 PLK1 (1.00) PLK1BRD4PLK3PTK2BRDT
Volasertib SCHEMBL18636896 1.00 PLK1 (1.00) PLK1BRD4PLK3PTK2BRDT
Volasertib SCHEMBL738946 1.00 PLK1 (1.00) PLK1BRD4PLK3PTK2BRDT
Volasertib SCHEMBL29363620 1.00 PLK1 (1.00) PLK1BRD4PLK3PTK2BRDT
Volasertib SCHEMBL18636919 1.00 PLK1 (1.00) PLK1BRD4PLK3PTK2BRDT
Volasertib SCHEMBL21916558 1.00 PLK1 (1.00) PLK1BRD4PLK3PTK2BRDT
Volasertib SCHEMBL29644957 0.99 PLK1 (0.99) PLK1BRD4PLK3PTK2BRDT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250129430-A1 HIGH ATP-AFFINITY PROTEIN AS THERAPEUTIC TARGET FOR INTRACTABLE CANCER MOLECULAR SUBTYPES AND INHIBITOR THEREOF VeraVerse Co., Ltd. (KR) 2025-04-24 US claimed
EP-4442840-A1 HIGH ATP-AFFINITY PROTEIN AS THERAPEUTIC TARGET FOR INTRACTABLE CANCER MOLECULAR SUBTYPES AND INHIBITOR THEREOF Veraverse Co., Ltd. (KR) 2024-10-09 EP claimed
WO-2023085716-A1 HIGH ATP-AFFINITY PROTEIN AS THERAPEUTIC TARGET FOR INTRACTABLE CANCER MOLECULAR SUBTYPES AND INHIBITOR THEREOF 연세대학교 산학협력단 2023-05-19 WO claimed
US-20260102359-A1 COMBINATION TREATMENT OF DERMAL AND TRANSDERMAL FIBROTIC DISEASES, DISORDERS AND ASSOCIATED PAIN AND INFLAMMATION ERESINA LLC (US) 2026-04-16 US disclosed
US-12390420-B1 Compositions for targeted delivery of therapeutic agents and methods for the synthesis and use thereof BRYET US, INC. (US) 2025-08-19 US disclosed
US-20250129430-A1 HIGH ATP-AFFINITY PROTEIN AS THERAPEUTIC TARGET FOR INTRACTABLE CANCER MOLECULAR SUBTYPES AND INHIBITOR THEREOF VeraVerse Co., Ltd. (KR) 2025-04-24 US disclosed
WO-2025074271-A1 MYT1 INHIBITORS FOR THE TREATMENT OF CANCERS HARBORING REPLICATION STRESS MUTATIONS REPARE THERAPEUTICS INC. (CA) 2025-04-10 WO disclosed
EP-4442840-A1 HIGH ATP-AFFINITY PROTEIN AS THERAPEUTIC TARGET FOR INTRACTABLE CANCER MOLECULAR SUBTYPES AND INHIBITOR THEREOF Veraverse Co., Ltd. (KR) 2024-10-09 EP disclosed
US-20230364097-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS INFINITY PHARMACEUTICALS, INC. (US) 2023-11-16 US disclosed
CN-117045660-A Application of PLK1 inhibitor in preparation of medicines for relieving kidney fibrosis 南京市儿童医院 2023-11-14 CN disclosed
WO-2023085716-A1 HIGH ATP-AFFINITY PROTEIN AS THERAPEUTIC TARGET FOR INTRACTABLE CANCER MOLECULAR SUBTYPES AND INHIBITOR THEREOF 연세대학교 산학협력단 2023-05-19 WO disclosed
US-20180015093-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS INFINITY PHARMACEUTICALS, INC. 2018-01-18 US disclosed
US-20170360795-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS INFINITY PHARMACEUTICALS, INC. (US) 2017-12-21 US disclosed
US-9567641-B2 Combination therapy for the treatment of cancer using an anti-C-met antibody SAMSUNG ELECTRONICS CO., LTD. (KR) 2017-02-14 US disclosed
US-20160113932-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS INFINITY PHARMACEUTICALS, INC. (US) 2016-04-28 US disclosed
US-20160024051-A1 SALTS AND SOLID FORMS OF ISOQUINOLINONES AND COMPOSITION COMPRISING AND METHODS OF USING THE SAME INFINITY PHARMACEUTICALS, INC. 2016-01-28 US disclosed
US-20150283142-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS INFINITY PHARMACEUTICALS, INC. (US) 2015-10-08 US disclosed
US-20150010575-A1 COMBINATION THERAPY FOR THE TREATMENT OF CANCER USING AN ANTI-C-MET ANTIBODY GEORGETOWN UNIVERSITY 2015-01-08 US disclosed
US-20140377258-A1 Treatment Of Cancers Using PI3 Kinase Isoform Modulators INFINITY PHARMACEUTICALS, INC. (US) 2014-12-25 US disclosed
US-8329695-B2 Crystalline form of the free base N-[trans-4-[4-(cyclopropylmethyl)-1-piperazinyl]cyclohexyl]-4-[[(7r)-7-ethyl-5,6,7,8-tetrahydro-5-methyl-8-(1-methylethyl)-6-oxo-2-pteridinyl]amino]-3-methoxy-benzamide BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2012-12-11 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 (10 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-20140377258-A1 Treatment Of Cancers Using PI3 Kinase Isoform Modulators PIK3CA, MCL1, PIK3CB PLK1 49/4885BRD4 1099/4885PLK3 359/4885
US-12390420-B1 Compositions for targeted delivery of therapeutic agents and methods for the synthesis and use thereof MSN, CD47, CTTN PLK1 304/4885BRD4 4644/4885PLK3 3751/4885
US-20150010575-A1 COMBINATION THERAPY FOR THE TREATMENT OF CANCER USING AN ANTI-C-MET ANTIBODY MET, HGF, HGFAC PLK1 1994/4885BRD4 2671/4885PLK3 3318/4885
US-20160113932-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS PIK3CA, PIK3CG, PIK3CD PLK1 276/4885BRD4 1751/4885PLK3 363/4885
US-20260102359-A1 COMBINATION TREATMENT OF DERMAL AND TRANSDERMAL FIBROTIC DISEASES, DISORDERS AND ASSOCIATED PAIN AND INFLAMMATION COL2A1, COLGALT1, PLOD3 PLK1 2955/4885BRD4 1044/4885PLK3 3287/4885
US-20150283142-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS PIK3CA, MCL1, PIK3CB PLK1 49/4885BRD4 1099/4885PLK3 359/4885
US-20170360795-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS PIK3CA, MCL1, PIK3CB PLK1 49/4885BRD4 1099/4885PLK3 359/4885
US-20230364097-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS PIK3CA, MCL1, PIK3CB PLK1 49/4885BRD4 1099/4885PLK3 359/4885
US-20180015093-A1 TREATMENT OF CANCERS USING PI3 KINASE ISOFORM MODULATORS PIK3CA, MCL1, PIK3CB PLK1 49/4885BRD4 1099/4885PLK3 359/4885
US-20160024051-A1 SALTS AND SOLID FORMS OF ISOQUINOLINONES AND COMPOSITION COMPRISING AND METHODS OF USING THE SAME PIK3CA, PIK3CD, JAK2 PLK1 57/4885BRD4 1022/4885PLK3 212/4885

“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.