Anlotinib Dihydrochloride
CAS No. 1360460-82-7
Anlotinib Dihydrochloride( Anlotinib (AL3818) dihydrochloride | AL3818 dihydrochloride )
Catalog No. M19393 CAS No. 1360460-82-7
Anlotinib also known as AL3818 is a receptor tyrosine kinase (RTK) inhibitor with potential antineoplastic and anti-angiogenic activities.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameAnlotinib Dihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionAnlotinib also known as AL3818 is a receptor tyrosine kinase (RTK) inhibitor with potential antineoplastic and anti-angiogenic activities.
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DescriptionAnlotinib also known as AL3818 is a receptor tyrosine kinase (RTK) inhibitor with potential antineoplastic and anti-angiogenic activities. Upon administration anlotininib targets multiple RTKs including vascular endothelial growth factor receptor type 2 (VEGFR2) and type 3 (VEGFR3). This agent may both inhibit angiogenesis and halt tumor cell growth.
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In Vitro——
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In Vivo——
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SynonymsAnlotinib (AL3818) dihydrochloride | AL3818 dihydrochloride
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PathwayAngiogenesis
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TargetVEGFR
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RecptorVEGFR2| VEGFR3|c-Kit
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Research AreaCancer
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IndicationNon-small cell lung Cancer
Chemical Information
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CAS Number1360460-82-7
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Formula Weight480.36
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Molecular FormulaC23H24Cl2FN3O3
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Purity>98% (HPLC)
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SolubilityDMSO:87 mg/mL(181.1 mM)
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SMILESCc1cc2c([nH]1)ccc(c2F)Oc1c2cc(c(cc2ncc1)OCC1(CC1)N)OC.Cl.Cl
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Vatalanib free base
A potent, orally available class III receptor tyrosine kinases inhibitor with IC50 of <1 uM for VEGFR, Flt-1, KDR and PDGFRβ.
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Lariciresinol
Lariciresinol is an enterolignan precursor, it possesses fungicidal activities by disrupting the fungal plasma membrane and therapeutic potential as a novel antifungal agent for the treatment of fungal infectious diseases in humans. Dietary lariciresinol can attenuate mammary tumor growth and reduce blood vessel density in human MCF-7 breast cancer xenografts and carcinogen-induced mammary tumors in rats.
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Sparteine sulfate
Sparteine sulfate is a class 1a antiarrhythmic agent and a sodium channel blocker. It can chelate the bivalents calcium and magnesium.
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