Diastovaricin I
| Code | Size | Price |
|---|
| BVT-0381-C500 | 500 ug | £110.00 |
Quantity:
| BVT-0381-M001 | 1 mg | £170.00 |
Quantity:
| BVT-0381-M005 | 5 mg | £490.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
-20°C
Documents
Further Information
Alternate Names/Synonyms:
30-Hydroxy-naphthomycin C
Appearance:
Orange to red powder.
CAS:
102281-52-7
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Hazards:
H302, H319
InChi:
InChI=1S/C39H45NO10/c1-20-11-9-7-8-10-12-30(44)40-33-37(48)27-18-25(6)36(47)32(31(27)38(49)39(33)50)35(46)24(5)17-23(4)34(45)22(3)14-16-26(41)15-13-21(2)29(43)19-28(20)42/h7-14,16-18,20,22-23,26,28,34,41-42,45,47,50H,15,19H2,1-6H3,(H,40,44)/b8-7+,11-9-,12-10-,16-14+,21-13+,24-17+/t20-,22-,23-,26-,28-,34-/m0/s1
InChiKey:
ODRXJBTZWPWLEA-AFALAGEISA-N
Long Description:
Chemical. CAS: 102281-52-7. Formula: C39H45NO10. MW: 687.8. Isolated from Streptomyces sp. G? 40/10. Antibiotic. Antibacterial. Inducer of Friend mouse erythroleukemia cells. Antitumor compound.
MDL:
MFCD01747732
Molecular Formula:
C39H45NO10
Molecular Weight:
687.8
Package Type:
Plastic Vial
Precautions:
P280, P301, P312, P305, P351, P338, P337, P313
Product Description:
Antibiotic. Antibacterial. Inducer of Friend mouse erythroleukemia cells. Antitumor compound.
Purity:
>98% (HPLC)
Signal word:
Warning
SMILES:
C[C@H]1C=C/C=C/C=CC(=O)NC2=C(O)C(=O)C3=C(C=C(C)C(O)=C3C(=O)C(C)=C[C@H](C)[C@@H](O)[C@@H](C)C=C[C@@H](O)CC=C(C)C(=O)C[C@@H]1O)C2=O
Solubility Chemicals:
Soluble in DMSO, acetone or chloroform.
Source / Host:
Isolated from Streptomyces sp. G? 40/10.
Transportation:
Non-hazardous
UNSPSC Category:
Natural Products/Extracts
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 1 year after receipt when stored at -20°C. Store solutions at -20°C in the dark.
References
Isolation and structural elucidation of naphthomycins B and C: W. Keller-Schierlein, et al.; J. Antibiot. 36, 484 (1983) | New ansamycin antibiotics, naphthoquinomycins A and B, inhibitors of fatty acid synthesis in escherichia coli: J.Mochizuki, et al.; J. Antibiot. 39, 157 (1986) | New ansamycin antibiotics, diastovaricins I and II: M. Hotta, et al.; J. Antibiot. 39, 311 (1986) | Cineromycins, gamma-butyrolactones and ansamycins by analysis of the secondary metabolite pattern created by a single strain of streptomyces: H.-J. Schiewe & A. Zeeck; J. Antibiot. 52, 635 (1999)
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