Cediranib

Cediranib

SCHEMBL63147

COc1cc2c(Oc3ccc4[nH]c(C)cc4c3F)ncnc2cc1OCCCN1CCCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FLT1FLT4KDRKITPDGFRAPDGFRB

The experimentally established mechanism targets of Cediranib. 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
KDR known ✓ P35968 11/20 1.00
FLT4 known ✓ P35916 5/20 1.00
FLT1 known ✓ P17948 4/20 1.00
PDGFRB known ✓ P09619 2/20 1.00
KIT known ✓ P10721 1/20 1.00
PDGFRA known ✓ P16234 1/20 1.00
RET P07949 4/20 1.00
TEK Q02763 2/20 1.00
AURKB Q96GD4 2/20 1.00
PLK4 O00444 1/20 1.00
GAK O14976 1/20 1.00
EPHB6 O15197 1/20 1.00
RIPK2 O43353 1/20 1.00
ERN1 O75460 1/20 1.00
STK10 O94804 1/20 1.00
MAP4K4 O95819 1/20 1.00
CHEK2 O96017 1/20 1.00
ABL1 P00519 1/20 1.00
EGFR P00533 1/20 1.00
ERBB2 P04626 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
Cediranib SCHEMBL29351458 1.00 KDR (1.00) KDRFLT4RETFLT1PDGFRB
Cediranib SCHEMBL29368143 1.00 KDR (1.00) KDRFLT4RETFLT1PDGFRB
Cediranib SCHEMBL29383181 1.00 KDR (1.00) KDRFLT4RETFLT1PDGFRB
SCHEMBL1685423 0.99 ABCB11 (1.00) KDRFLT4RETFLT1PDGFRB
SCHEMBL20077514 0.94 KDR (0.89) KDRFLT4RETFLT1PDGFRB
Cediranib SCHEMBL4186434 0.94 KDR (0.89) KDRFLT4RETFLT1PDGFRB
SCHEMBL3198096 0.94 KDR (0.89) KDRFLT4RETFLT1PDGFRB
SCHEMBL13471998 0.94 KDR (0.89) KDRFLT4RETFLT1PDGFRB
SCHEMBL1401668 0.94 KDR (0.89) KDRFLT4RETFLT1PDGFRB
SCHEMBL1401641 0.93 KDR (0.88) KDRFLT4RETFLT1PDGFRB

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 1926 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116059312-A Integrin GPIIb/IIIa antagonists and their use in combination with anti-VEGF antibodies 百奥泰生物制药股份有限公司 2023-05-05 CN claimed
US-20230091105-A1 CHIMERIC FUSIONS BETWEEN C4-BINDING PROTEIN C-TERMINAL SEGMENT AND ANGIOPOIETIN-1 FIBRINOGEN-LIKE DOMAIN AS ANGIOPOIETIN MIMETICS AND TIE2 AGONISTS TO TREAT VASCULAR DISEASES UNIV NORTHWESTERN (US) 2023-03-23 US claimed
WO-2023001288-A1 INTEGRIN GPIIB/IIIA ANTAGONIST AND APPLICATION THEREOF IN COMBINATION WITH ANTI-VEGF ANTIBODY 百奥泰生物制药股份有限公司 2023-01-26 WO claimed
EP-4110796-A1 CHIMERIC FUSIONS BETWEEN C4-BINDING PROTEIN C-TERMINAL SEGMENT AND ANGIOPOIETIN-1 FIBRINOGEN-LIKE DOMAIN AS ANGIOPOIETIN MIMETICS AND TIE2 AGONISTS TO TREAT VASCULAR DISEASES Northwestern University (US) 2023-01-04 EP claimed
CN-115485290-A Chimeric fusions between C-terminal segments of C4-binding proteins and angiopoietin-1 fibrinogen-like domains as angiopoietin mimetics and Tie2 agonists for the treatment of vascular disease 西北大学 2022-12-16 CN claimed
WO-2022245061-A1 BENZAMIDE DERIVATIVE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION FOR PREVENTION OR TREATMENT OF CANCER CONTAINING SAME AS ACTIVE INGREDIENT 에이치케이이노엔 주식회사 2022-11-24 WO claimed
US-20210363231-A1 OPTIMIZED ANTIBODY COMPOSITIONS FOR TREATMENT OF OCULAR DISORDERS GENENTECH INC (US) 2021-11-25 US claimed
US-20210115124-A1 OPTIMIZED VARIANTS OF ANTI-VEGF ANTIBODIES GENENTECH INC (US) 2021-04-22 US claimed
US-20200222547-A1 HYDROGEL CROSS-LINKED HYALURONIC ACID PRODRUG COMPOSITIONS AND METHODS GENENTECH, INC. (US) 2020-07-16 US claimed
CN-110891611-A Hydrogel cross-linked hyaluronic acid prodrug compositions and methods 基因泰克公司 2020-03-17 CN claimed
US-20060223815-A1 Therapeutic agents comprising an anti-angiogenic agent in combination with an src-inhibitor and their therapeutic use ASTRAZENECA AB (SE) 2006-10-05 US claimed
US-7074800-B1 Quinazoline derivatives as angiogenesis inhibitors ASTRAZENECA AB (SE) 2006-07-11 US claimed
US-20060135486-A1 Use of sulfonamide-including compounds in combination with angiogenesis inhibitors EISAI CO., LTD. (JP) 2006-06-22 US claimed
EP-1620104-A1 THERAPEUTIC AGENTS COMPRISING AN ANTI-ANGIOGENIC AGENT IN COMBINATION WITH AN SRC-INHIBITOR AND THEIR THERAPEUTIC USE Astrazeneca AB (SE) 2006-02-01 EP claimed
EP-1553097-A1 QUINAZOLINE DERIVATIVES AS ANGIOGENESIS INHIBITORS AND INTERMEDIATES THEREFORE AstraZeneca AB (SE) 2005-07-13 EP claimed
EP-1154774-B1 QUINAZOLINE DERIVATIVES AS ANGIOGENESIS INHIBITORS ASTRAZENECA AB (SE) 2005-06-22 EP claimed
WO-2004098604-A1 THERAPEUTIC AGENTS COMPRISING AN ANTI-ANGIOGENIC AGENT IN COMBINATION WITH AN SRC-INHIBITOR AND THEIR THERAPEUTIC USE ASTRAZENECA AB (SE) 2004-11-18 WO claimed
US-20030144298-A1 Using a combination of an angiogenisis inhibitor and a hypotensive agent for use in treating diseases associated with angiogenesis; an endothelial growth factor receptor tyrosine kinase inhibitor; antidiabetic, -arthritis agents ASTRAZENECA AB (SE) 2003-07-31 US claimed
EP-1272186-A1 THERAPEUTIC COMBINATIONS OF ANTIHYPERTENSIVE AND ANTIANGIOGENIC AGENTS AstraZeneca AB (SE) 2003-01-08 EP claimed
WO-2001074360-A1 THERAPEUTIC COMBINATIONS OF ANTIHYPERTENSIVE AND ANTIANGIOGENIC AGENTS ASTRAZENECA AB (SE) 2001-10-11 WO 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 (6 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-20060135486-A1 Use of sulfonamide-including compounds in combination with angiogenesis inhibitors FLT4, KDR, FLT1 KDR 2/4885FLT4 1/4885FLT1 3/4885
US-20210363231-A1 OPTIMIZED ANTIBODY COMPOSITIONS FOR TREATMENT OF OCULAR DISORDERS VEGFA, CD44, UACA KDR 7/4885FLT4 6/4885FLT1 8/4885
US-20060223815-A1 Therapeutic agents comprising an anti-angiogenic agent in combination with an src-inhibitor and their therapeutic use SRC, TEK, FLT4 KDR 5/4885FLT4 3/4885FLT1 4/4885
US-20200222547-A1 HYDROGEL CROSS-LINKED HYALURONIC ACID PRODRUG COMPOSITIONS AND METHODS CD44, HCAR3, HPSE KDR 1364/4885FLT4 1584/4885FLT1 1107/4885
US-20210115124-A1 OPTIMIZED VARIANTS OF ANTI-VEGF ANTIBODIES VEGFA, FLT4, FLT1 KDR 4/4885FLT4 2/4885FLT1 3/4885
US-20030144298-A1 Using a combination of an angiogenisis inhibitor and a hypotensive agent for use in treating diseases associated with angiogenesis; an endothelial growth factor receptor tyrosine kinase inhibitor; antidiabetic, -arthritis agents TEK, TIE1, FLT1 KDR 5/4885FLT4 4/4885FLT1 3/4885

“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.