Trichoviridin
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
| Category | Antibiotics |
| Catalog number | BBF-02714 |
| CAS | 56283-32-0 |
| Molecular Weight | 183.16 |
| Molecular Formula | C8H9NO4 |
Online Inquiry
Capabilities & Facilities
Fermentation Lab
4 R&D and scale-up labs
2 Preparative purification labs
Fermentation Plant
Semi pilot, pilot and industrial plant 4 Manufacturing sites 7 Production lines at pilot scale 100+ Reactors of 30-4000 L; 170+ reactors of 20 KL-30 KL; 24+ reactors of >100 KL 2 Hydrogenation reactors (200 L, 4Mpa and 1000L, 4Mpa)
Product Description
It is originally isolated from Trichoderma viride. Trichoviridin has anti-bacterial and fungal effects.
- Specification
- Properties
- Reference Reading
- Price Product List
| Synonyms | Isonitrin C; Trichoviridine |
| IUPAC Name | (1R,2S,4R,5R,6S)-5-[(1S)-1-hydroxyethyl]-1-isocyano-3,7-dioxatricyclo[4.1.0.02,4]heptan-5-ol |
| Canonical SMILES | CC(C1(C2C(O2)C3(C1O3)[N+]#[C-])O)O |
| InChI | InChI=1S/C8H9NO4/c1-3(10)7(11)4-5(12-4)8(9-2)6(7)13-8/h3-6,10-11H,1H3/t3-,4+,5-,6-,7+,8+/m0/s1 |
| InChI Key | GVXPCFBDZAWTNL-NOVZGDRXSA-N |
| Appearance | Pale Yellow Acicular Crystal |
| Antibiotic Activity Spectrum | fungi |
| Melting Point | 95-96°C |
1. Ovine ill-thrift in Nova Scotia. 9. Production of experimental quantities of isocyanide metabolites of Trichoderma hamatum
D Brewer, A Feicht, A Taylor, J W Keeping, A A Taha, V Thaller Can J Microbiol. 1982 Nov;28(11):1252-60. doi: 10.1139/m82-186.
Laboratory cultures of Trichoderma hamatum produce metabolites that are characterized by an isocyanide functionality. Three such metabolites predominate. One is the known compound trichoviridin (I). The other two, described here for the first time, are 3-(3-isocyano-6-oxabicyclo[3,1,0]hex-2-en-5-yl)acrylic acid (II) and a very unstable compound 3-(3-isocyanocyclopent-2-enylidene-)propionic acid (III). Production of these three metabolites by a random sample of wild isolates of the fungus has been examined. At least one of these isocyanides was isolated from all cultures in which the culture broth inhibited the growth of Micrococcus luteus. The relative amounts of the three isocyanides produced by individual isolates were not the same and cultures were found in which I, II, or III was the main product. The isocyanide III was produced by all wild isolates which had antibiotic activity in their culture broth, and it was present in the concentration range 2-40 mg X L-1.
| BBF-05751 | Cyclosporin L | Inquiry |
| BBF-05853 | Palbociclib | Inquiry |
| BBF-01829 | Deoxynojirimycin | Inquiry |
| BBF-04727 | Strigolactone GR24 | Inquiry |
| BBF-04609 | 1,1-Dimethylbiguanide hydrochloride | Inquiry |
| BBF-03756 | Amygdalin | 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
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 ╳
