Adavosertib

Adavosertib

SCHEMBL1504444

C=CCn1c(=O)c2cnc(Nc3ccc(N4CCN(C)CC4)cc3)nc2n1-c1cccc(C(C)(C)O)n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

WEE1

The experimentally established mechanism targets of Adavosertib. 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
WEE1 known ✓ P30291 20/20 1.00
PLK1 P53350 6/20 1.00
PKMYT1 Q99640 2/20 1.00
GAK O14976 1/20 1.00
EPHB6 O15197 1/20 1.00
JAK2 O60674 1/20 1.00
PRKD3 O94806 1/20 1.00
MAP4K4 O95819 1/20 1.00
PAK4 O96013 1/20 1.00
ABL1 P00519 1/20 1.00
LCK P06239 1/20 1.00
FYN P06241 1/20 1.00
CYP3A4 P08684 1/20 1.00
WEE2 P0C1S8 1/20 1.00
BCR P11274 1/20 1.00
CSNK2A2 P19784 1/20 1.00
SYK P43405 1/20 1.00
CSNK1A1 P48729 1/20 1.00
NEK2 P51955 1/20 1.00
NEK3 P51956 1/20 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
Adavosertib SCHEMBL29381006 1.00 WEE1 (1.00) WEE1PLK1PKMYT1GAKEPHB6
Adavosertib SCHEMBL30559444 1.00 WEE1 (1.00) WEE1PLK1PKMYT1GAKEPHB6
Adavosertib SCHEMBL1504996 0.99 WEE1 (0.98) WEE1PLK1PKMYT1GAKEPHB6
Adavosertib SCHEMBL1504998 0.99 WEE1 (0.98) WEE1PLK1PKMYT1GAKEPHB6
SCHEMBL25890930 0.98 WEE1 (0.96) WEE1PLK1PKMYT1GAKEPHB6
SCHEMBL1815951 0.97 WEE1 (0.94) WEE1PLK1PKMYT1GAKEPHB6
Adavosertib SCHEMBL3579242 0.97 WEE1 (0.94) WEE1PLK1PKMYT1GAKEPHB6
SCHEMBL1811019 0.94 WEE1 (0.89) WEE1PLK1PKMYT1GAKEPHB6
SCHEMBL1813967 0.94 WEE1 (0.89) WEE1PLK1PKMYT1GAKEPHB6
SCHEMBL15959140 0.94 WEE1 (0.89) WEE1PLK1PKMYT1GAKEPHB6

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 2042 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12637720-B2 Molecular subtyping of small cell lung cancer to predict therapeutic responses BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2026-05-26 US claimed
WO-2026104998-A1 SUBSTITUTED IMIDAZOPYRIDINE COMPOUND DERIVATIVES AND THEIR PHARMACEUTICAL USE AVELOS THERAPEUTICS INC. (KR) 2026-05-21 WO claimed
WO-2025217307-A9 METHODS FOR PREDICTING RESPONSE TO A RAS(ON) INHIBITOR AND COMBINATION THERAPIES Revolution Medicines, Inc. (US) 2026-05-15 WO claimed
EP-4735448-A1 SUBSTITUTED SPIRO COMPOUND DERIVATIVES AND THEIR PHARMACEUTICAL USE Avelos Therapeutics Inc. (KR) 2026-05-06 EP 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-3850004-B1 NATURAL KILLER CELL COMPOSITIONS AND IMMUNOTHERAPY METHODS FOR TREATING A LIVER TUMOR NKARTA INC (US) 2026-02-18 EP claimed
EP-4688775-A1 SUBSTITUTED SULTAM COMPOUND DERIVATIVES AND THEIR PHARMACEUTICAL USE Avelos Therapeutics Inc. (KR) 2026-02-11 EP claimed
US-20260009798-A1 METHODS AND SYSTEMS FOR TREATING DISEASE USING AN ATR/CHK1 SIGNALING PATHWAY INHIBITOR ACRIVON THERAPEUTICS INC (US) 2026-01-08 US claimed
US-20250387643-A1 METHODS AND APPARATUS FOR APPLYING TUMOR TREATING FIELDS COMBINED WITH PERSONALIZED ULTRA-FRACTIONATED STEREOTACTIC ADAPTIVE RADIOTHERAPY THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2025-12-25 US claimed
WO-2010076887-A1 PREDICTIVE BIOMARKERS USEFUL FOR CANCER THERAPY MEDIATED BY A WEE1 INHIBITOR BANYU PHARMACEUTICAL CO.,LTD. (JP) 2010-07-08 WO claimed
US-20100124544-A1 CRYSTALLINE FORMS OF DIHYDROPYRAZOLOPYRIMIDINONE MERCK & CO., INC. 2010-05-20 US claimed
US-20100063024-A1 Dihydropyrazolopyrimidinone Derivatives MERCK SHARP & DOHME LLC 2010-03-11 US claimed
EP-2155752-A1 POLYMORPH OF DIHYDROPYRAZOLOPYRIMIDINONE DERIVATIVE AS WEEL KINASE.INHIBITOR Merck & Co., Inc. (US) 2010-02-24 EP claimed
EP-2016080-A4 DIHYDROPYRAZOLOPYRIMIDINONE DERIVATIVES BANYU PHARMA CO LTD (JP) 2009-05-13 EP claimed
EP-2016080-A1 DIHYDROPYRAZOLOPYRIMIDINONE DERIVATIVES BANYU PHARMACEUTICAL CO., LTD. (JP) 2009-01-21 EP claimed
EP-2017278-A1 DIHYDROPYRAZOLOPYRIMIDINONE DERIVATIVE BANYU PHARMACEUTICAL CO., LTD. (JP) 2009-01-21 EP claimed
WO-2008133866-A1 POLYMORPH OF DIHYDROPYRAZOLOPYRIMIDINONE DERIVATIVE AS WEEL KINASE.INHIBITOR MERCK & CO., INC. (US) 2008-11-06 WO claimed
WO-2007126122-A1 DIHYDROPYRAZOLOPYRIMIDINONE DERIVATIVES BANYU PHARMACEUTICAL CO., LTD. (JP) 2007-11-08 WO claimed
US-20070254892-A1 Dihydropyrazolopyrimidinone derivatives MSD K.K. (JP) 2007-11-01 US claimed