Get A Quote

Halymecin B

* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

Category Others
Catalog number BBF-01316
CAS 167173-81-1
Molecular Weight 967.18
Molecular Formula C48H86O19

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 produced by the strain of Fusarium sp. FE-71-1.

  • Specification
  • Properties
  • Reference Reading
  • Price Product List
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.

Bio Calculators

Stock concentration: *
Desired final volume: *
Desired concentration: *

L

* 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
g/mol
g

Recently viewed products

Online Inquiry

Copyright © 2025 BOC Sciences. All rights reserved.

cartIcon
Inquiry Basket