Chaetoviridin A
| Code | Size | Price |
|---|
| BVT-0419-M001 | 1 mg | £135.00 |
Quantity:
| BVT-0419-M005 | 5 mg | £470.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C
Documents
Further Information
Alternate Names/Synonyms:
CCRIS 7226
Appearance:
Yellow to orange powder.
CAS:
128252-98-2
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Hazards:
H302, H312, H319
InChi:
InChI=1S/C23H25ClO6/c1-6-11(2)7-8-14-9-15-16(10-29-14)18-17(20(26)12(3)13(4)25)22(28)30-23(18,5)21(27)19(15)24/h7-13,25H,6H2,1-5H3/b8-7+/t11-,12+,13+,23-/m0/s1
InChiKey:
HWSQVPGTQUYLEQ-LYUOGRNPSA-N
Long Description:
Chemical. CAS: 128252-98-2. Formula: C23H25ClO6. MW: 432.9. Isolated from Chaetomium sp. Azaphilone antibiotic. Antifungal compound (phytopathogenic fungi). Cholesteryl ester transfer protein (CETP) inhibitor. Improves blood lipid levels. Monoamine oxidase inhibitor.
MDL:
MFCD02752487
Molecular Formula:
C23H25ClO6
Molecular Weight:
432.9
Package Type:
Plastic Vial
Precautions:
P270, P280, P301, P312, P302, P352, P312
Product Description:
Azaphilone antibiotic. Antifungal compound (phytopathogenic fungi). Cholesteryl ester transfer protein (CETP) inhibitor. Improves blood lipid levels. Monoamine oxidase inhibitor.
Purity:
>96% (HPLC)
Signal word:
Warning
SMILES:
O=C1C(C([C@H](C)[C@@H](C)O)=O)=C2C3=COC(/C=C/[C@@H](C)CC)=CC3=C(Cl)C([C@@]2(C)O1)=O
Solubility Chemicals:
Soluble in DMSO, methanol, chloroform or acetone.
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 -20°C.
References
Four new azaphilones from Chaetomium globosum var. flavor-viridae: M. Takahashi, et al.; Chem. Pharm. Bull. 38, 625 (1990) | Structure-specific inhibition of cholesteryl ester transfer protein by azaphilones: H. Tomoda, et al.; J. Antibiot. 52, 160 (1999) | Antifungal activity against plant pathogenic fungi of chaetoviridins isolated from Chaetomium globosum: J.-H. Park, et al.; FEMS Microbiol. Lett. 252, 309 (2005) | Bis-spiro-azaphilones and azaphilones from the fungi Chaetomium cochliodes VTh01 and C. cochliodes CTh05: N. Phonkerd, et al.; Tetrahedron 64, 9636 (2008) | Azaphilones, a class of fungal metabolites with diverse biological activities: N. Osmanova, et al.; Phytochem. Rev. 9, 315 (2010) | Azaphilones from the endophyte Chaetomium globosum: W. S. Borges, et al.; J. Nat. Prod. 74, 1182 (2011) | Identification and characterization of the chaetoviridin and chaetomugilin gene cluster in Chaetomium globosum: J. M. Winter, et al.; JACS 134, 17900 (2012) | New azaphilones from Chaetomium globosum isolated from the built environment: D. R. McMullin, et al.; Tetrahedron Lett. 54, 568 (2013) | Potentially harmful secondary metabolites produced by indoor Chaetomium species on artificially and naturally contaminated building materials: I. Dosen, et al.; Indoor Air 27, 34 (2017) | Total Synthesis and Structural Revision of Chaetoviridins A: M. Makrerougras, et al.; Org. Lett. 19, 4146 (2017) | New metabolites from endophytic fungus Chaetomium globosum CDW7: W. Yan, et al.; Molecules 23, 2873 (2018) | The screening and identification of the biological control fungi Chaetomium spp. against wheat common root rot: H.-M. Yue, et al.; FEMS Microbiol. Lett. 365, fny242 (2018)
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