Accéder au contenu
MilliporeSigma
Toutes les photos(3)

Key Documents

N9162

Sigma-Aldrich

Neocarzinostatin

from Streptomyces carzinostaticus, ≥90% (SDS-PAGE), solution

Synonyme(s) :

Holoneocarzinostatin, NCS, NSC-69856, Zinostatin

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme


About This Item

Numéro CAS:
Numéro MDL:
Code UNSPSC :
12352200
Nomenclature NACRES :
NA.77

product name

Neocarzinostatin from Streptomyces carzinostaticus, ≥90% (SDS-PAGE), ~0.5 mg/mL

Niveau de qualité

Pureté

≥90% (SDS-PAGE)

Forme

solution

Concentration

~0.5 mg/mL

Spectre d'activité de l'antibiotique

neoplastics

Mode d’action

DNA synthesis | interferes

Conditions d'expédition

wet ice

Température de stockage

2-8°C

InChI

1S/C35H35NO12/c1-16-12-19(42-4)14-22-20(16)8-9-23(37)27(22)32(40)45-24-13-18-10-11-35(26-15-43-34(41)46-26)25(48-35)7-5-6-21(18)31(24)47-33-28(36-3)30(39)29(38)17(2)44-33/h8-9,12-14,17,21,24-26,28-31,33,36-39H,6,15H2,1-4H3/t17-,21?,24-,25-,26-,28-,29+,30-,31-,33-,35+/m1/s1

Clé InChI

BLXZMHNVKCEIJX-PNKAXBHOSA-N

Application

Neocarzinostatin from Streptomyces carzinostaticus has been used:
  • as a DNA damaging agent to treat human fibroblast GM0637 cells
  • as a radiomimetic antibiotic to induce DNA damage
  • in combination with Vγ2Vδ2 T cells to determine the cytotoxicity in ovarian cancer cells

Actions biochimiques/physiologiques

Neocarzinostatin is a protein-small molecule complex composed of an enediyne chromophore tightly bound to a 113 amino acid single chain protein. The complex possesses antiproliferative and antitumor activity. The chromophore is the active compound, which is responsible for DNA cleavage; while the apoprotein stabilizes and regulates the availability of the labile chromophore. NCS chromophore is bound non-covalently in a cleft of the binding protein and is dissociable. Upon addition of a thiol, the chromophore forms a highly reactive biradical species that can induce sequence-specific single and double strand breaks in DNA. Neocarzinostatin inhibits DNA synthesis and possesses antitumor activity in various human and animal tumors. NCS inhibits cellular proliferation by inducing G2 cell cycle arrest and apoptosis in both human papillomavirus (HPV) positive and negative cell lines.
Neocarzinostatin is a radiomimetic antibiotic substance.

Forme physique

Supplied as 100 μg (~9 nmoles) in a solution containing 20 mM MES buffer, pH 5.5.

Code de la classe de stockage

10 - Combustible liquids

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Long non-coding RNA ANRIL (CDKN2B-AS) is induced by the ATM-E2F1 signaling pathway
Wan G, et al.
Cellular Signalling, 25(5), 1086-1095 (2013)
B Heyd et al.
Journal of bacteriology, 182(7), 1812-1818 (2000-03-14)
Neocarzinostatin (NCS) is the most studied member of a family of chromoproteins secreted by a range of actinomycetes species. It has been proposed that in addition to their antitumoral activity related to the bound chromophores, this group of related proteins
Induction of ATM/ATR pathway combined with Vgamma2Vdelta2 T cells enhances cytotoxicity of ovarian cancer cells
Lu J,et al.
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, 1842(7), 1071-1079 (2014)
Neocarzinostatin-chromophore: a potent inhibitor of casein kinase II in vitro.
Tanoue, S., et al.
Antibiotics, 51, 95-98 (1998)
The enediyne antibiotics.
A L Smith et al.
Journal of medicinal chemistry, 39(11), 2103-2117 (1996-05-24)

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique