Parvisporin
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
| Category | Others |
| Catalog number | BBF-02956 |
| CAS | |
| Molecular Weight | 390.51 |
| Molecular Formula | C23H34O5 |
Online Inquiry
Description
It is a neuritogenic agent produced by the strain of Stachyborrys parvispora F4708. It promotes the enlargement of the neural sinus of P12 cells, and the effect of Stachybotrin C is obvious, but the effect of Parvisporin is weak.
Specification
| IUPAC Name | 2,4-dihydroxy-6-(hydroxymethyl)-3-[(2E,6E)-11-hydroxy-3,7,11-trimethyldodeca-2,6-dienyl]benzaldehyde |
| Canonical SMILES | CC(=CCCC(=CCC1=C(C=C(C(=C1O)C=O)CO)O)C)CCCC(C)(C)O |
| InChI | InChI=1S/C23H34O5/c1-16(9-6-12-23(3,4)28)7-5-8-17(2)10-11-19-21(26)13-18(14-24)20(15-25)22(19)27/h7,10,13,15,24,26-28H,5-6,8-9,11-12,14H2,1-4H3/b16-7+,17-10+ |
| InChI Key | IOIZASRPFAFSMJ-CHGLLVKUSA-N |
Properties
| Appearance | Pale Yellow to White Powder |
| Melting Point | 73-75°C |
| Solubility | Soluble in Methanol |
Reference Reading
1. Stachybotrin C and parvisporin, novel neuritogenic compounds. I. Taxonomy, isolation, physico-chemical and biological properties
Y Nozawa, K Yamamoto, M Ito, N Sakai, K Mizoue, F Mizobe, K Hanada J Antibiot (Tokyo). 1997 Aug;50(8):635-40. doi: 10.7164/antibiotics.50.635.
Stachybotrin C and parvisporin, novel neuritogenic compounds, were isolated from the culture broth of Stachybotrys parvispora F4708. Stachybotrin C induced significant neurite outgrowth in PC12 cells and showed cell survival activity in the primary culture of cerebral cortical neurons. Parvisporin demonstrated only weak neuritogenic activity.
2. Stachybotrin C and parvisporin, novel neuritogenic compounds. II. Structure determination
Y Nozawa, M Ito, K Sugawara, K Hanada, K Mizoue J Antibiot (Tokyo). 1997 Aug;50(8):641-5. doi: 10.7164/antibiotics.50.641.
The structures of stachybotrin C and parvisporin have been determined by spectroscopic analyses and chemical derivatization. Stachybotrin C contains a unique pyrano-isoindolinone ring system, while parvisporin has a hydroxyl farnesyl phenol structure.
Recommended Products
| BBF-03755 | Actinomycin D | Inquiry |
| BBF-03754 | CASTANOSPERMINE | Inquiry |
| BBF-02642 | Lactonamycin | Inquiry |
| BBF-05862 | Epirubicin | Inquiry |
| BBF-01825 | Loganin | Inquiry |
| BBF-01693 | Doxorubicin EP Impurity A (Daunorubicin) | Inquiry |
Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
Recently viewed products
Penicillin | Axenomycin B | Duocarmycin B2 | 1,8-Cyclotetradecadiene-1-carboxylic acid, 5-(hydroxymethyl)-12-(1-hydroxy-1-methylethyl)-9-methyl-, methyl ester, [5S-(5R*,8Z,12S*)]- | Echinomycin | Echinoserine | A-500359H | 2,4,5-Tri-O-methylhiascic acid | Desisobutyrylfidaxomicin | Megalomicin B | Parvisporin
