Benin
CAS No. 22181-94-8
Benin( Butocin | Butocine )
Catalog No. M24003 CAS No. 22181-94-8
Benin is an effective cytostatic drug used for the treatment of generalized carcinoma of the breast.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 542 | In Stock |
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| 5MG | 493 | In Stock |
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| 10MG | 678 | In Stock |
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| 25MG | 1007 | In Stock |
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| 50MG | 1321 | In Stock |
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| 100MG | 1776 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameBenin
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NoteResearch use only, not for human use.
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Brief DescriptionBenin is an effective cytostatic drug used for the treatment of generalized carcinoma of the breast.
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DescriptionBenin is an effective cytostatic drug used for the treatment of generalized carcinoma of the breast.(In Vitro):Benin is a cytostatic drug, but inactive in the standard plate incorporation method of Ames reversion test using four Salmonella typhimurium strains.
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In Vitro——
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In Vivo——
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SynonymsButocin | Butocine
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number22181-94-8
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Formula Weight337.4
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Molecular FormulaC14H19N5O3S
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESCCOC(=O)CNC(=O)CCCCSC1=NC=NC2=C1NC=N2
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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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CL2A-SN-38 DCA 127...
CL2A-SN-38 is a drug-linker conjugate composed of a potent a DNA Topoisomerase I inhibitor SN-38 and a linker CL2A to make antibody drug conjugate (ADC).
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MM 54
Potent apelin receptor antagonist (Ki = 82 nM; IC50 = 93 nM). Antagonizes the inhibitory affect of [Pyr1]-Apelin-13 on forskolin-induced cAMP accumulation in CHO-K1-APJ cells. Recuces tumor expansion and lengthens survival time in a mouse xenograft model of glioblastoma.
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Aminoadipic acid
Aminoadipic acid (2-aminoadipate) is a metabolite in the principal biochemical pathway of lysine. It is an intermediate in the metabolism of lysine and saccharopine. It antagonizes neuroexcitatory activity modulated by the glutamate receptor N-methyl-D-aspartate (NMDA).
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