19-O-Acetylchaetoglobosin A

Bioviotica
Product Code: BVT-0383
Supplier: Bioviotica
CodeSizePrice
BVT-0383-M0011 mg£110.00
Quantity:
BVT-0383-M0055 mg£315.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Antibody Isotype: n/a
Antibody Clone: n/a
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C

Images

1 / 1
Chemical Structure

Chemical Structure

Further Information

Appearance:
Yellow solid.
CAS:
50939-69-0
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
After reconstitution protect from light at -20°C.Protect from light.
Hazards:
H302, H312, H319
InChi:
InChI=1S/C34H38N2O6/c1-18-9-8-11-24-31-33(5,42-31)20(3)29-26(16-22-17-35-25-12-7-6-10-23(22)25)36-32(40)34(24,29)28(39)14-13-27(38)30(19(2)15-18)41-21(4)37/h6-8,10-15,17-18,20,24,26,29-31,35H,9,16H2,1-5H3,(H,36,40)/b11-8+,14-13+,19-15-/t18-,20-,24-,26-,29-,30+,31-,33+,34+/m0/s1
InChiKey:
AZLAYOMQTNEYFJ-PWPDRILLSA-N
Long Description:
Chemical. CAS: 50939-69-0. Formula: C34H38N2O6. MW: 570.7. Isolated from Chaetomium sp. Cytochalasan alkaloid, derivative of chaetoglobosin A (Prod. No. BVT-0092 http://www.adipogen.com/bvt-0092/chaetoglobosin-a.html ). Mycotoxin. Phytotoxin.
Molecular Formula:
C34H38N2O6
Molecular Weight:
570.7
Package Type:
Plastic Vial
Precautions:
P270, P280, P301, P312, P302, P352, P312
Product Description:
Cytochalasan alkaloid, derivative of chaetoglobosin A (Prod. No. BVT-0092 http://www.adipogen.com/bvt-0092/chaetoglobosin-a.html ). Mycotoxin. Phytotoxin.
Purity:
>98% (HPLC, NMR)
Signal word:
Warning
SMILES:
[H][C@]12[C@H](CC3=CNC4=CC=CC=C34)NC(=O)[C@]11C(=O)C=CC(=O)[C@H](OC(C)=O)C(C)=C/[C@@H](C)CC=C[C@@]1([H])[C@@H]1O[C@]1(C)[C@H]2C
Solubility Chemicals:
Soluble in DMSO, acetone or dichloromethane. Fairly soluble in water or methanol.
Source / Host:
Isolated from Chaetomium sp.
Transportation:
Non-hazardous
UNSPSC Category:
Natural Products/Extracts
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 1 year after receipt when stored at +4°C. After reconstitution protect from light at -20°C.

References

19-O-Acetylchaetoglobosin B and 19-O-Acetylchaetoglobosin D, Two New Metabolites of Chaetomium globosum: A. Probst & C. Tamm; Helv. Chim. Acta 64, 2056 (1981) | Biosynthesis of the cytochalasans. Biosynthetic studies on chaetoglobosin A and 19-O-acetylchaetoglobosin A: A. Probst & C. Tamm; Helv. Chim. Acta 64, 2065 (1981) | Chaetoglobosins, cytotoxic 10-(indol-3-yl)-[13]cytochalasans from Chaetomium spp. I. production, isolation and some cytological effects of chaetoglobosin A-J: S. Sekita, et al.; Chem. Pharm. Bull. 30, 1609 (1982) | Chaetoglobosins, cytotoxic 10-(indol-3-yl)-[13]cytochalasans from chaetomium spp. II Structures of chaetoglobosins A, B, and D: S. Sekita, et al.; Chem. Pharm. Bull. 30, 1618 (1982) | Structure-activity relationship of thirty-nine cytochalasans observed in the effects on cellular structures and cellular event and on actin polymerization in vitro: S. Sekita, et al.; J. Pharmacobio-Dynam. 8, 906 (1985) | Phytotoxic chaetoglobosins are produced by the plant pathogen Calonectria morganii (anamorph Cylindrocladium scoparium): C. Wallbrunn, et al.; J. Gen. Appl. Microbiol. 47, 33 (2001) | Combinatorial generation of complexity by redox enzymes in the chaetoglobosin A biosynthesis: K. Ishiuchi, et al.; JACS 135, 7371 (2013)

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