Halymecin B
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| Category | Others |
| Catalog number | BBF-01316 |
| CAS | 167173-81-1 |
| Molecular Weight | 967.18 |
| Molecular Formula | C48H86O19 |
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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 produced by the strain of Fusarium sp. FE-71-1.
- Specification
- Properties
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| Synonyms | Decanoic acid, 3-(acetyloxy)-5-[[3-hydroxy-5-[[5-hydroxy-3-(b-D-mannopyranosyloxy)-1-oxodecyl]oxy]-1-oxodecyl]oxy]-, 1-(3-carboxy-2-hydroxypropyl)hexyl ester, [3R-[1[R*(R*)],3R*,5R*[3R*,5R*(3R*,5R*)]]]- |
| IUPAC Name | (3R,5R)-5-[(3R,5R)-3-acetyloxy-5-[(3R,5R)-3-hydroxy-5-[(3R,5R)-5-hydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxydecanoyl]oxydecanoyl]oxydecanoyl]oxy-3-hydroxydecanoic acid |
| Canonical SMILES | CCCCCC(CC(CC(=O)OC(CCCCC)CC(CC(=O)OC(CCCCC)CC(CC(=O)OC(CCCCC)CC(CC(=O)O)O)OC(=O)C)O)OC1C(C(C(C(O1)CO)O)O)O)O |
| InChI | InChI=1S/C48H86O19/c1-6-10-14-18-32(51)22-38(66-48-47(61)46(60)45(59)40(30-49)67-48)28-43(57)64-36(20-16-12-8-3)24-34(53)26-42(56)65-37(21-17-13-9-4)27-39(62-31(5)50)29-44(58)63-35(19-15-11-7-2)23-33(52)25-41(54)55/h32-40,45-49,51-53,59-61H,6-30H2,1-5H3,(H,54,55)/t32-,33-,34-,35-,36-,37-,38-,39-,40-,45-,46+,47+,48-/m1/s1 |
| InChI Key | NOMDKESBADZKCR-WYFDDTMZSA-N |
| Appearance | Colorless Oily Matter |
| Solubility | Soluble in Dichloromethane |
1. Halymecins, new antimicroalgal substances produced by fungi isolated from marine algae
C Chen, N Imamura, M Nishijima, K Adachi, M Sakai, H Sano J Antibiot (Tokyo). 1996 Oct;49(10):998-1005. doi: 10.7164/antibiotics.49.998.
Novel antimicroalgal substances halymecins A (1), B (2) and C (3) were isolated from the fermentation broth of a Fusarium sp. and halymecins D (4) and E (5) from an Acremonium sp. The structures of these halymecins, Fig. 1, were determined based on extensive 2D NMR studies as well as mass spectral data. These chemical structures are conjugates of di- and trihydroxydecanoic acid. Halymecin A showed antimicroalgal activity against Skeletonema costatum.
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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 ╳
