Cediranib

Cediranib

SCHEMBL1218429

COc1cc2c(Oc3ccc4[nH]c(C)cc4c3F)ncnc2cc1OCCCN1CCCC1.O=C(O)C=CC(=O)O

nearest known ligand 0.87

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 0.87
▸ FLT1 known ✓ P17948 5/20 0.87
▸ FLT4 known ✓ P35916 5/20 0.87
▸ PDGFRB known ✓ P09619 1/20 0.87
▸ KIT known ✓ P10721 1/20 0.87
▸ PDGFRA known ✓ P16234 1/20 0.87
▸ RET P07949 4/20 0.87
▸ PLK4 O00444 1/20 0.87
▸ GAK O14976 1/20 0.87
▸ EPHB6 O15197 1/20 0.87
▸ RIPK2 O43353 1/20 0.87
▸ ERN1 O75460 1/20 0.87
▸ STK10 O94804 1/20 0.87
▸ MAP4K4 O95819 1/20 0.87
▸ CHEK2 O96017 1/20 0.87
▸ ABL1 P00519 1/20 0.87
▸ EGFR P00533 1/20 0.87
▸ ERBB2 P04626 1/20 0.87
▸ LCK P06239 1/20 0.87
▸ FYN P06241 1/20 0.87

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 SCHEMBL23924949 1.00 KDR (0.87) KDRFLT1FLT4RETPLK4
Cediranib SCHEMBL1218427 1.00 KDR (0.87) KDRFLT1FLT4RETPLK4
Cediranib SCHEMBL29351942 1.00 KDR (0.87) KDRFLT1FLT4RETPLK4
Cediranib SCHEMBL63147 0.93 KDR (1.00) KDRFLT1FLT4RETPLK4
Cediranib SCHEMBL29383181 0.93 KDR (1.00) KDRFLT1FLT4RETPLK4
Cediranib SCHEMBL29351458 0.93 KDR (1.00) KDRFLT1FLT4RETPLK4
Cediranib SCHEMBL29368143 0.93 KDR (1.00) KDRFLT1FLT4RETPLK4
SCHEMBL1685423 0.92 ABCB11 (1.00) KDRFLT1FLT4RETPLK4
SCHEMBL1401646 0.88 KDR (0.81) KDRFLT1FLT4RETPLK4
SCHEMBL297569 0.88 KDR (0.81) KDRFLT1FLT4RETPLK4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20180170913-A1 MALEATE SALTS OF A QUINAZOLINE DERIVATIVE USEFUL AS AN ANTIANGIOGENIC AGENT ASTRAZENECA AB (SE) 2018-06-21 — — US claimed
US-9890140-B2 Maleate salts of a quinazoline derivative useful as an antiangiogenic agent ASTRAZENECA AB (SE) 2018-02-13 — — US claimed
US-9556151-B2 Maleate salts of a quinazoline derivative useful as an antiangiogenic agent ASTRAZENECA AB (SE) 2017-01-31 — — US claimed
EP-1699782-B1 MALEATE SALTS OF A QUINAZOLINE DERIVATIVE USEFUL AS AN ANTIANGIOGENIC AGENT ASTRAZENECA AB (SE) 2010-06-23 — — EP claimed
US-20180170913-A1 MALEATE SALTS OF A QUINAZOLINE DERIVATIVE USEFUL AS AN ANTIANGIOGENIC AGENT ASTRAZENECA AB (SE) 2018-06-21 — — US disclosed
US-9890140-B2 Maleate salts of a quinazoline derivative useful as an antiangiogenic agent ASTRAZENECA AB (SE) 2018-02-13 — — US disclosed
US-9556151-B2 Maleate salts of a quinazoline derivative useful as an antiangiogenic agent ASTRAZENECA AB (SE) 2017-01-31 — — US disclosed
US-20150025091-A1 Maleate Salts of a Quinazoline Derivative Useful as an Antiangiogenic Agent ASTRAZENECA AB (SE) 2015-01-22 — — US disclosed
US-8859570-B2 Maleate salts of a quinazoline derivative useful as an antiangiogenic agent ASTRAZENECA AB (SE) 2014-10-14 — — US disclosed
US-8754240-B2 Process for the manufacture of 4-fluoro-2-methyl-1H-indol-5-ol ASTRAZENECA AB (SE) 2014-06-17 — — US disclosed
EP-2540705-A2 Process for preparing indol-5-oxy-quinazoline derivatives and intermediates AstraZeneca AB (Publ) (SE) 2013-01-02 — — EP disclosed
EP-2540706-A2 PROCESS FOR PREPARING INDOL-5-OXY-QUINAZOLINE DERIVATIVES AND INTERMEDIATES AstraZeneca AB (Publ) (SE) 2013-01-02 — — EP disclosed
US-7851623-B2 Chemical process ASTRAZENECA AB (SE) 2010-12-14 — — US disclosed
US-20100298357-A1 MALEATE SALTS OF A QUINAZOLINE DERIVATIVE USEFUL AS AN ANTIANGIOGENIC AGENT ASTRAZENECA AB (SE) 2010-11-25 — — US disclosed
EP-1699782-B1 MALEATE SALTS OF A QUINAZOLINE DERIVATIVE USEFUL AS AN ANTIANGIOGENIC AGENT ASTRAZENECA AB (SE) 2010-06-23 — — EP disclosed
EP-2129657-A2 PROCESS FOR PREPARING INDOL-5-OXY-QUINAZOLINE DERIVATIVES AND INTERMEDIATES AstraZeneca AB (SE) 2009-12-09 — — EP disclosed
WO-2009104019-A1 COMBINATION THERAPY 238 ASTRAZENECA AB (SE) 2009-08-27 — — WO disclosed
US-20080221322-A1 CHEMICAL PROCESS ASTRAZENECA AB (SE) 2008-09-11 — — US disclosed
WO-2008053221-A2 PROCESS FOR PREPARING INDOL- 5 -OXY- QUINAZOLINE DERIVATIVES AND INTERMEDIATES ASTRAZENECA AB (SE) 2008-05-08 — — WO disclosed
US-20070129387-A1 Maleate salts of a quinazoline derivative useful as an antiangiogenic agent ASTRAZENECA AB (SE) 2007-06-07 — — 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 (5 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-20180170913-A1 MALEATE SALTS OF A QUINAZOLINE DERIVATIVE USEFUL AS AN ANTIANGIOGENIC AGENT FLT1, TEK, FLT4 KDR 4/4885FLT1 1/4885FLT4 3/4885
US-20100298357-A1 MALEATE SALTS OF A QUINAZOLINE DERIVATIVE USEFUL AS AN ANTIANGIOGENIC AGENT FLT1, TEK, FLT4 KDR 4/4885FLT1 1/4885FLT4 3/4885
US-20150025091-A1 Maleate Salts of a Quinazoline Derivative Useful as an Antiangiogenic Agent FLT1, TEK, FLT4 KDR 4/4885FLT1 1/4885FLT4 3/4885
US-20070129387-A1 Maleate salts of a quinazoline derivative useful as an antiangiogenic agent FLT1, TEK, FLT4 KDR 4/4885FLT1 1/4885FLT4 3/4885
US-20080221322-A1 CHEMICAL PROCESS CYP3A5, CYP3A4, CYP3A7 KDR 3684/4885FLT1 3138/4885FLT4 1887/4885

“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.

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