Danusertib

Danusertib

SCHEMBL466509

CO[C@@H](C(=O)N1Cc2[nH]nc(NC(=O)c3ccc(N4CCN(C)CC4)cc3)c2C1)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AURKAAURKBAURKC

The experimentally established mechanism targets of Danusertib. 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
AURKA known ✓ O14965 18/20 1.00
AURKB known ✓ Q96GD4 8/20 1.00
AURKC known ✓ Q9UQB9 2/20 1.00
ABL1 P00519 4/20 1.00
CDK2 P24941 4/20 1.00
NTRK1 P04629 3/20 1.00
RET P07949 3/20 1.00
FGFR1 P11362 3/20 1.00
LIMK1 P53667 3/20 1.00
BCR P11274 3/20 1.00
FLT3 P36888 3/20 1.00
PLK4 O00444 2/20 1.00
JAK2 O60674 2/20 1.00
MAP4K4 O95819 2/20 1.00
LCK P06239 2/20 1.00
FYN P06241 2/20 1.00
FES P07332 2/20 1.00
LYN P07948 2/20 1.00
SRC P12931 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
Danusertib SCHEMBL2685432 1.00 AURKA (1.00) AURKAAURKBABL1CDK2NTRK1
Danusertib SCHEMBL29453494 0.99 AURKA (0.98) AURKAAURKBABL1CDK2NTRK1
SCHEMBL1377925 0.92 AURKA (0.86) AURKAAURKBABL1CDK2NTRK1
SCHEMBL26184014 0.92 AURKA (0.86) AURKAAURKBABL1CDK2NTRK1
SCHEMBL9998664 0.92 AURKA (0.86) AURKAAURKBABL1CDK2NTRK1
SCHEMBL25277403 0.92 AURKA (0.86) AURKAAURKBABL1CDK2NTRK1
SCHEMBL1377947 0.92 AURKA (0.85) AURKAAURKBABL1CDK2NTRK1
SCHEMBL3486691 0.92 AURKA (0.85) AURKAAURKBABL1CDK2NTRK1
SCHEMBL3486749 0.92 AURKA (0.85) AURKAAURKBABL1CDK2NTRK1
SCHEMBL2922037 0.92 AURKA (0.85) AURKAAURKBABL1CDK2NTRK1

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 2133 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122057044-A Nanometer liposome delivery system for targeting PLK1/Aurora kinase and application thereof in oral squamous cell carcinoma treatment 徐州医科大学 2026-05-19 CN claimed
EP-4729519-A1 CRYSTAL FORM OF ENPP1 INHIBITOR CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. (CN) 2026-04-22 EP claimed
US-12577255-B2 MDM2-based modulators of proteolysis and associated methods of use ARVINAS OPERATIONS, INC. (US) 2026-03-17 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
EP-4704832-A2 BIFUNCTIONAL SMALL MOLECULES TO TARGET THE SELECTIVE DEGRADATION OF CIRCULATING PROTEINS Biohaven Therapeutics Ltd. (VG) 2026-03-11 EP claimed
WO-2026043541-A1 COMPOSITIONS AND METHODS FOR TREATING CANCER TUFTS MEDICAL CENTER, INC. (US) 2026-02-26 WO claimed
US-20260022117-A1 COMPOUNDS AND METHODS FOR THE ENHANCED DEGRADATION OF TARGETED PROTEINS ARVINAS OPERATIONS INC (US) 2026-01-22 US claimed
EP-4667458-A1 PHARMACEUTICAL COMPOSITION FOR TREATMENT OF CANCER, COMPRISING SOS1 INHIBITOR AND ANTICANCER DRUG Kanaph Therapeutics Inc. (KR) 2025-12-24 EP claimed
US-12485178-B2 Bifunctional small molecules to target the selective degradation of circulating proteins YALE UNIVERSITY (US) 2025-12-02 US 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
EP-2788504-B1 METHOD OF DETERMINATION OF CANCER CELL DRUG SENSITIVITY TOWARDS AURORA KINASE INHIBITORS PALACKY UNIVERSITY OLOMOUC (CZ) 2016-08-17 EP claimed
US-20140336073-A1 METHOD OF DETERMINATION OF CANCER CELL DRUG SENSITIVITY TOWARDS AURORA KINASE INHIBITORS PALACKY UNIVERSITY, OLOMOUC (CZ) 2014-11-13 US claimed
EP-2602330-A1 Method of determination of cancer cell drug sensitivity towards Aurora kinase inhibitors and overcoming their resistance Palacky University, Olomouc (CZ) 2013-06-12 EP claimed
US-8084455-B2 Use of a kinase inhibitor for the treatment of particular resistant tumors NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2011-12-27 US claimed
EP-1644376-B1 PYRROLO 3,4-c PYRAZOLE DERIVATIVES ACTIVE AS KINASE INHIBITORS NERVIANO MEDICAL SCIENCES SRL (IT) 2010-09-08 EP claimed
US-20100035876-A1 Use of a Kinase Inhibitor for the Treatment of Particular Resistant Tumors NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2010-02-11 US claimed
EP-2004180-A2 USE OF A KINASE INHIBITOR FOR THE TREATMENT OF PARTICULAR RESISTANT TUMORS Nerviano Medical Sciences S.r.l. (IT) 2008-12-24 EP claimed
WO-2007113212-A2 USE OF A KINASE INHIBITOR FOR THE TREATMENT OF PARTICULAR RESISTANT TUMORS NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2007-10-11 WO claimed
US-7141568-B2 Pyrrolo[3,4-c]pyrazole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them PFIZER ITALIA S.R.L. (IT) 2006-11-28 US claimed
US-20050032839-A1 Pyrrolo[3,4-c]pyrazole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them PHARMACIA ITALIA S.P.A. (IT) 2005-02-10 US claimed