Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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C125911-10mg | 10mg | In stock | $105.90 | |
C125911-50mg | 50mg | In stock | $224.90 |
Synonyms | AZD2171 | NSC755606 | NSC-755606 | MFCD09954115 | Recentin | Cediranib - AZD2171 | D08881 | N-acetyl-N-formyl-5-methoxykynuramine | XXJWYDDUDKYVKI-UHFFFAOYSA-N | A24280 | AZD 2171 | HY-10205 | ZD-2171 | SCHEMBL157630 | 4-(4-Fluoro-2-methyl-1H-indol-5-ylox |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | Cediranib is VEGFR2 inhibitor. Cediranib inhibited VEGF-stimulated proliferation and KDR phosphorylation with IC50s of 0.4 and 0.5 nM, respectively. |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Vascular endothelial growth factor receptor inhibitor |
Product Description | Cediranib (AZD2171) is a highly potent VEGFR(KDR) inhibitor with IC50 of <1 nM, also inhibits Flt1/4 with IC50 of 5 nM/≤3 nM, similar activity against c-Kit and PDGFRβ, 36-, 110-fold and >1000-fold selective more for VEGFR than PDGFR-α, CSF-1R and Flt3, Phase 3. |
ALogP | 4.9 |
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IUPAC Name | 4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline |
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INCHI | InChI=1S/C25H27FN4O3/c1-16-12-17-19(29-16)6-7-21(24(17)26)33-25-18-13-22(31-2)23(14-20(18)27-15-28-25)32-11-5-10-30-8-3-4-9-30/h6-7,12-15,29H,3-5,8-11H2,1-2H3 |
InChi Key | XXJWYDDUDKYVKI-UHFFFAOYSA-N |
Canonical SMILES | CC1=CC2=C(N1)C=CC(=C2F)OC3=NC=NC4=CC(=C(C=C43)OC)OCCCN5CCCC5 |
Isomeric SMILES | CC1=CC2=C(N1)C=CC(=C2F)OC3=NC=NC4=CC(=C(C=C43)OC)OCCCN5CCCC5 |
PubChem CID | 9933475 |
Molecular Weight | 450.52 |
CAS Registry No. | 288383-20-0 |
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Wikipedia | Cediranib |
DiscoveRx TREEspot | AZD-2171| |
PubChem CID | 9933475 |
ChEMBL Ligand | CHEMBL491473 |
Reactome Reaction | R-HSA-2023462, R-HSA-2029992 |
Reactome Drug | R-ALL-2023377 |
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Solubility | DMSO 90 mg/mL Water <1 mg/mL Ethanol <1 mg/mL |
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Pictogram(s) | GHS06, GHS08, GHS09, GHS07 |
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Signal | Danger |
Hazard Statements | H315:Causes skin irritation H301:Toxic if swallowed H312:Harmful in contact with skin H410:Very toxic to aquatic life with long lasting effects H372:Causes damage to organs through prolonged or repeated exposure H361:Suspected of damaging fertility or the unborn child |
Precautionary Statements | P273:Avoid release to the environment. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P405:Store locked up. P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P260:Do not breathe dust/fume/gas/mist/vapors/spray. P270:Do not eat, drink or smoke when using this product. P362+P364:Take off contaminated clothing and wash it before reuse. P391:Collect spillage. P330:Rinse mouth. P203:Obtain, read and follow all safety instructions before use. P301+P316:IF SWALLOWED: Get emergency medical help immediately. P318:if exposed or concerned, get medical advice. P317:Get emergency medical help. P332+P317:If skin irritation occurs: Get medical help. P319:Get medical help if you feel unwell. |
1. Wedge SR, Kendrew J, Hennequin LF, Valentine PJ, Barry ST, Brave SR, Smith NR, James NH, Dukes M, Curwen JO et al.. (2005) AZD2171: a highly potent, orally bioavailable, vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor for the treatment of cancer.. Cancer Res, 65 (10): (4389-400). [PMID:15899831] [10.1021/op500134e] |