B5507

Bleomycin sulfate from Streptomyces verticillus

crystalline, 1.5-2.0 U/mg

Manufacturer: Sigma Aldrich

CAS Number: 9041-93-4

Synonym(S): Blenoxane, Bleo, Blexane

Select a Size

Pack Size SKU Availability Price
15 UNITS B5507-15-UNITS In Stock ₹ 1,06,539.65

B5507 - 15 UNITS

₹ 1,06,539.65

In Stock

Quantity

1

Base Price: ₹ 1,06,539.65

GST (18%): ₹ 19,177.137

Total Price: ₹ 1,25,716.787

form

crystalline

Quality Level

200

specific activity

1.5-2.0 U/mg

color

white to off-white

solubility

H2O: 20 mg/mL

cation traces

Cu: ≤0.10%

antibiotic activity spectrum

fungi

Mode of action

DNA synthesis | interferes

storage temp.

2-8°C

SMILES string

[O-]S([O-])(=O)=O.C[C@@H](O)[C@@H](NC(=O)[C@@H](C)[C@H](O)[C@@H](C)NC(=O)[C@H](NC(=O)c1nc(nc(N)c1C)[C@H](CC(N)=O)NC[C@H](N)C(N)=O)[C@@H](O[C@@H]2O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]2O[C@@H]3O[C@H](CO)[C@@H](O)[C@@H](OC(N)=O)[C@@H]3O)c4c[nH]cn4)C(=O)NCCc5nc(cs5)-c6ncc(s6)C(=O)NCCC[S+](C)C.C[C@@H](O)[C@@H](NC(=O)[C@@H](C)[C@H](O)[C@@H](C)NC(=O)[C@H](NC(=O)c7nc(nc(N)c7C)[C@H](CC(N)=O)NC[C@H](N)C(N)=O)[C@@H](O[C@@H]8O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]8O[C@@H]9O[C@H](CO)[C@@H](O)[C@@H](OC(N)=O)[C@@H]9O)c%10c[nH]cn%10)C(=O)NCCc%11nc(cs%11)-c%12ncc(s%12)C(=O)NCCC[S+](C)C

Other Options

Image Product Name Manufacturer Price Range
BP971
Bleomycin sulfate
Sigma Aldrich ₹ 21,974.75
1076308
Bleomycin sulfate
Sigma Aldrich ₹ 82,648.88
B2434
Bleomycin sulfate from Streptomyces verticillus
Sigma Aldrich ₹ 1,56,020.73
B8416
Bleomycin sulfate from Streptomyces verticillus
Sigma Aldrich ₹ 1,32,032.53
15361
Bleomycin sulfate from Streptomyces verticillus
Sigma Aldrich ₹ 21,671.65 - ₹ 99,871.45

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Description

  • General description: Bleomycin Sulfate is an antineoplastic antibiotic isolated from Streptomyces verticillus.[1] It is recommended for use as a cell culture agent at 10-100 μg/mL.
  • Application: Bleomycin Sulfate is an atineoplastic antibiotic isolated from Streptomyces verticillus. It is recommended for use as a cell culture agent at 10-100 μg/mL.
  • Biochem/physiol Actions: Bleomycin sulfate binds to DNA, causes ssDNA scission at specific base sequences and inhibits DNA synthesis. This inhibitory action requires bleomycin to bind oxygen and a metal ion. It can also cleave RNA, to a lesser degree but more selectively. It acts as an inducer and regulator of apoptosis and inhibits tumor angiogenesis.
  • Features and Benefits: This compound is a featured product for Apoptosis research. Click here to discover more featured Apoptosis products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
  • Components: This product is a mixture of glycopeptides antibiotics containing Bleomycin A2 (70%) and B2(30%). Bleomycins differ from each other in the terminal amine and show varying biological activity.
  • Caution: This product should be stored at 2-8°C.
  • Preparation Note: The product is soluble in water in water at 20 mg/mL and is active for several days. A solution of 2 units/mL in 0.1 M neutral potassium phosphate should be used within 14 days. A solution is active for three months at 3 units/mL in normal saline.
  • Other Notes: Keep container tightly closed in a dry and well-ventilated place, strongly hygroscopic

SAFETY INFORMATION

Pictograms

GHS08

Signal Word

Danger

Hazard Statements

H340,H351,H361fd

Precautionary Statements

P201 - P202 - P280 - P308 + P313 - P405 - P501

Hazard Classifications

Carc. 2 - Muta. 1B - Repr. 2

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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[O-]S([O-])(=O)=O.C[C@@H](O)[C@@H](NC(=O)[C@@H](C)[C@H](O)[C@@H](C)NC(=O)[C@H](NC(=O)c1nc(nc(N)c1C)[C@H](CC(N)=O)NC[C@H](N)C(N)=O)[C@@H](O[C@@H]2O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]2O[C@@H]3O[C@H](CO)[C@@H](O)[C@@H](OC(N)=O)[C@@H]3O)c4c[nH]cn4)C(=O)NCCc5nc(cs5)-c6ncc(s6)C(=O)NCCC[S+](C)C.C[C@@H](O)[C@@H](NC(=O)[C@@H](C)[C@H](O)[C@@H](C)NC(=O)[C@H](NC(=O)c7nc(nc(N)c7C)[C@H](CC(N)=O)NC[C@H](N)C(N)=O)[C@@H](O[C@@H]8O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]8O[C@@H]9O[C@H](CO)[C@@H](O)[C@@H](OC(N)=O)[C@@H]9O)c%10c[nH]cn%10)C(=O)NCCc%11nc(cs%11)-c%12ncc(s%12)C(=O)NCCC[S+](C)C

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