Home > Products > Agrochemicals > Agrochemical Intermediates > (Z)-5-((5-FLUORO-2-OXOINDOLIN-3-YLIDENE)METHYL)-N-(2-HYDROXY-3-MORPHOLINOPROPYL)-2,4-DIMETHYL-1H-PYRROLE-3-CARBOXAMIDE
(Z)-5-((5-FLUORO-2-OXOINDOLIN-3-YLIDENE)METHYL)-N-(2-HYDROXY-3-MORPHOLINOPROPYL)-2,4-DIMETHYL-1H-PYRROLE-3-CARBOXAMIDE structure, CAS 627908-92-3

(Z)-5-((5-FLUORO-2-OXOINDOLIN-3-YLIDENE)METHYL)-N-(2-HYDROXY-3-MORPHOLINOPROPYL)-2,4-DIMETHYL-1H-PYRROLE-3-CARBOXAMIDE

CAS Number627908-92-3

SynonymsSU14813

Molecular FormulaC23H27O4N4F1

Molecular Weight442.49

Purity96+%

Density

Boiling Point

Melting Point

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EINECS0

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Cat. No.: 2A-0102478 Purity: 96+%
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Quality Control of [ 627908-92-3 ] Purity: 96+% SDS Specification MoL

Chemical & Physical Properties
CAS Number627908-92-3
Catalog No.2A-0102478
Chinese NameSU14813
SynonymsSU14813
Molecular FormulaC23H27O4N4F1
Molecular Weight442.49
Purity96+
Storage Condition2-8℃
ApplicationSU14813 is a multi-target receptor tyrosine kinase inhibitor with IC50 values ​​of 50, 2, 4 and 15 nM for inhibiting VEGFR2, VEGFR1, PDGFRβ and KIT respectively.
EINECS0
HTC2934999090
UN(IATA)0
MDL NumberMFCD19704841
SMILESCc1[nH]c(C=C2C(=O)Nc3ccc(F)cc32)c(C)c1C(=O)NCC(O)CN1CCOCC1
InChI KeyCTNPALGJUAXMMC-INIZCTEOSA-N
MSDSmsds/102478_1_627908_92_3.pdf
Use ofSU14813 is a multi-targeted receptor tyrosine kinases inhibitor with IC50s of 50, 2, 4, 15 nM for VEGFR2, VEGFR1, PDGFRβ and KIT. Properties Name 5-[(Z)-(5-Fluoro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)methyl]-N-[ 2-hydroxy-3-(4-morpholinyl)propyl]-2,4-dimethyl-1H-pyrrole-3-carb oxamide Synonym More Synonyms SU14813 Biological Activity Description SU14813 is a multi-targeted receptor tyrosine kinases inhibitor with IC50s of 50, 2, 4, 15 nM for VEGFR2, VEGFR1, PDGFRβ and KIT. Related Catalog Signaling Pathways >> Protein Tyrosine Kinase/RTK >> c-Kit Signaling Pathways >> Protein Tyrosine Kinase/RTK >> PDGFR Research Areas >> Cancer VEGFR1:2 nM (IC50) VEGFR2:50 nM (IC50) PDGFRβ:4 nM (IC50) KIT:15 nM (IC50) In Vivo SU14813 inhibits VEGFR-2, PDGFR-β, and FLT3 phosphorylation in xenograft tumors in a dose- and time-dependent fashion. The plasma concentration required for in vivo target inhibition is estimated to be 100 to 200 ng/mL. Used as monotherapy, SU14813 exhibits broad and potent antitumor activity resulting in regression, growth arrest, or substantially reduces growth of various established xenografts derived from human or rat tumor cell lines. Treatment in combination with docetaxel significantly enhances both the inhibition of primary tumor growth and the survival of the tumor-bearing mice compared with administration of either agent alone[1]. References [1]. Patyna S, et al. SU14813: a novel multiple receptor tyrosine kinase inhibitor with potent antiangiogenic and antitumor activity. Mol Cancer Ther. 2006 Jul;5(7):1774-82. Chemical & Physical Properties Molecular Formula C23H27FN4O4 Exact Mass 442.20200 PSA 113.67000 LogP 2.28400 InChIKey CTNPALGJUAXMMC-INIZCTEOSA-N Storage condition 2-8℃ Safety Information HS Code 2934999090
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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