Quizartinib

Quizartinib

SCHEMBL742377

CC(C)(C)c1cc(NC(=O)Nc2ccc(-c3cn4c(n3)sc3cc(OCCN5CCOCC5)ccc34)cc2)no1.Cl.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CSF1RFLT3KITPDGFRAPDGFRBRET

The experimentally established mechanism targets of Quizartinib. 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
FLT3 known ✓ P36888 20/20 1.00
CSF1R known ✓ P07333 1/20 0.99
RET known ✓ P07949 1/20 0.99
PDGFRB known ✓ P09619 1/20 0.99
KIT known ✓ P10721 1/20 0.99
PDGFRA known ✓ P16234 1/20 0.99
KDR P35968 2/20 1.00
BMPR1B O00238 1/20 0.99
MUSK O15146 1/20 0.99
EPHB6 O15197 1/20 0.99
MAP3K7 O43318 1/20 0.99
RIPK2 O43353 1/20 0.99
PAK3 O75914 1/20 0.99
STK10 O94804 1/20 0.99
MAP4K4 O95819 1/20 0.99
ABL1 P00519 1/20 0.99
NTRK1 P04629 1/20 0.99
LCK P06239 1/20 0.99
YES1 P07947 1/20 0.99
LYN P07948 1/20 0.99

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
Quizartinib SCHEMBL29435035 1.00 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL74121 1.00 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL72923 0.99 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL29349937 0.99 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Hydrochloric Acid SCHEMBL3453696 0.97 FLT3 (0.99) FLT3KDRBMPR1BMUSKEPHB6
SCHEMBL73633 0.96 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Hydrochloric Acid SCHEMBL742748 0.95 FLT3 (0.99) FLT3KDRBMPR1BMUSKEPHB6
Hydrochloric Acid SCHEMBL74122 0.95 FLT3 (0.99) FLT3KDRBMPR1BMUSKEPHB6
SCHEMBL72924 0.94 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Hydrochloric Acid SCHEMBL74399 0.94 FLT3 (0.99) FLT3KDRBMPR1BMUSKEPHB6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4743086-A2 TREATING MYELOID DISORDERS Mayo Foundation for Medical Education and Research (US) 2026-05-20 EP claimed
EP-4638443-A1 TRANSIENT RECEPTOR POTENTIAL VANILLOID 6 INHIBITORS Uniquest Pty Limited (AU) 2025-10-29 EP claimed
WO-2025015263-A2 TREATING MYELOID DISORDERS MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2025-01-16 WO claimed
US-20240282425-A1 AUTHENTICATION METHODS AND SYSTEMS FOR DISPENSED PRESCRIPTIONS LOW GORDON KEITH (US) 2024-08-22 US claimed
WO-2024130344-A1 TRANSIENT RECEPTOR POTENTIAL VANILLOID 6 INHIBITORS UNIQUEST PTY LIMITED (AU) 2024-06-27 WO claimed
EP-3260119-B1 COMBINATION METHOD FOR TREATING CANCER DAIICHI SANKYO CO LTD (JP) 2023-11-15 EP claimed
US-10716790-B2 Method for treating cancer by combined use DAIICHI SANKYO COMPANY, LIMITED (JP) 2020-07-21 US claimed
EP-2521782-B1 FLT3 RECEPTOR ANTAGONISTS FOR THE TREATMENT OR THE PREVENTION OF PAIN DISORDERS INST NAT SANTE RECH MED (FR) 2019-04-10 EP claimed
EP-2903593-B1 TABLET CONTAINING COMPOSITE WITH CYCLODEXTRIN AMBIT BIOSCIENCES CORP (US) 2018-03-21 EP claimed
EP-3260119-A1 COMBINATION METHOD FOR TREATING CANCER DAIICHI SANKYO COMPANY, LIMITED (JP) 2017-12-27 EP claimed
US-20170216302-A1 METHOD FOR TREATING CANCER BY COMBINED USE DAIICHI SANKYO COMPANY, LIMITED (JP) 2017-08-03 US claimed
US-9675549-B2 Tablet containing composite with cyclodextrin AMBIT BIOSCIENCES CORPORATION (US) 2017-06-13 US claimed
US-20150250720-A1 TABLET CONTAINING COMPOSITE WITH CYCLODEXTRIN DAIICHI SANKYO COMPANY, LIMITED (JP) 2015-09-10 US claimed
US-9109227-B2 FLT3 receptor antagonists for the treatment or the prevention of pain disorders INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (FR) 2015-08-18 US claimed
EP-4743086-A2 TREATING MYELOID DISORDERS Mayo Foundation for Medical Education and Research (US) 2026-05-20 EP disclosed
US-20260130893-A1 PRMT5 INHIBITORS AND USES THEREOF GILEAD SCIENCES INC (US) 2026-05-14 US disclosed
EP-4735445-A1 KRAS MODULATING COMPOUNDS GILEAD SCIENCES, INC. (US) 2026-05-06 EP disclosed
EP-2429524-A1 METHODS OF TREATING PROLIFERATIVE DISEASES Ambit Biosciences Corporation (US) 2012-03-21 EP disclosed
WO-2011083124-A1 FLT3 RECEPTOR ANTAGONISTS FOR THE TREATMENT OR THE PREVENTION OF PAIN DISORDERS INSERM (Institut National de la Santé et de la Recherche Médicale) (FR) 2011-07-14 WO disclosed
WO-2010132787-A1 METHODS OF TREATING PROLIFERATIVE DISEASES AMBIT BIOSCIENCES CORPORATION (US) 2010-11-18 WO 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 (4 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-20150250720-A1 TABLET CONTAINING COMPOSITE WITH CYCLODEXTRIN HBZ, MCL1, HBB FLT3 23/4885CSF1R 2846/4885RET 2600/4885
US-20260130893-A1 PRMT5 INHIBITORS AND USES THEREOF PRMT5, PRMT1, PRMT6 FLT3 1906/4885CSF1R 1226/4885RET 892/4885
US-20170216302-A1 METHOD FOR TREATING CANCER BY COMBINED USE FLT3, MDM2, TP53 FLT3 1/4885CSF1R 185/4885RET 78/4885
US-10716790-B2 Method for treating cancer by combined use FLT3, MDM2, TP53 FLT3 1/4885CSF1R 185/4885RET 78/4885

“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.