Vinblastine sulfate

CAS No. 143-67-9

Vinblastine sulfate ( 29060LE; Alkaban-AQ; Exal; NSC 49842; Rozevinsulfate; Velban; Velsar )

Catalog No. M11857 CAS No. 143-67-9

Vinblastine sulfate can inhibit the formation of microtubule, it also inhibit nAChR(IC50=8.9 uM).

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 45 In Stock
10MG 49 In Stock
25MG 58 In Stock
50MG 76 In Stock
100MG 87 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Vinblastine sulfate
  • Note
    Research use only, not for human use.
  • Brief Description
    Vinblastine sulfate can inhibit the formation of microtubule, it also inhibit nAChR(IC50=8.9 uM).
  • Description
    Vinblastine sulfate can inhibit the formation of microtubule, it also inhibit nAChR(IC50=8.9 uM).
  • Synonyms
    29060LE; Alkaban-AQ; Exal; NSC 49842; Rozevinsulfate; Velban; Velsar
  • Pathway
    Endocrinology/Hormones
  • Target
    AChR
  • Recptor
    nAChR
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    143-67-9
  • Formula Weight
    909.06
  • Molecular Formula
    C46H58N4O9·H2SO4
  • Purity
    >98%(HPLC)
  • Solubility
    Soluble in DMSO
  • SMILES
    CC[C@@]1(C[C@@H]2C[C@@](C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)[C@]78CCN9[C@H]7[C@@](C=CC9)([C@H]([C@@]([C@@H]8N6C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)O.OS(=O)(=O)O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Gigant B, et al. Nature, 2005, 435(7041), 519-522.
molnova catalog
related products
  • Atropine sulfate mon...

    Atropine sulfate monohydrate is a competitive muscarinic acetylcholine receptor antagonist.

  • Zolpidem Tartrate

    Zolpidem is a prescription medication used for the treatment of insomnia and some brain disorders.

  • Catestatin

    Non-competitive nicotinic cholinergic antagonist; selectively inhibits nicotinic-stimulated catecholamine secretion from chromaffin cells and noradrenergic neurons (IC50 ~ 200 nM). Blocks nicotinic-induced cationic signaling (IC50 ~ 200 - 250 nM) and inhibits nicotinic-agonist induced desensitization of catecholamine release. Also stimulates mast cell release of histamine via a separate mechanism.