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851671

Sigma-Aldrich

Helicin

99%

Synonym(s):

Salicylaldehyde β-D-glucoside

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About This Item

Empirical Formula (Hill Notation):
C13H16O7
CAS Number:
618-65-5
Molecular Weight:
284.26
EC Number:
210-558-9
MDL number:
MFCD00006589
UNSPSC Code:
12352200
PubChem Substance ID:
24888215
NACRES:
NA.22

assay

99%

form

solid

optical activity

[α]25/D −57.1°, c = 1.5 in H2O

mp

178 °C (lit.)

SMILES string

[H]C(=O)c1ccccc1O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O

InChI

1S/C13H16O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-5,9-13,15-18H,6H2/t9-,10-,11+,12-,13-/m1/s1

InChI key

BGOFCVIGEYGEOF-UJPOAAIJSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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Line Christiansen et al.
Applied and environmental microbiology, 86(21) (2020-08-23)
Pseudomonas fluorescens In5 synthesizes the antifungal cyclic lipopeptides (CLPs) nunamycin and nunapeptin, which are similar in structure and genetic organization to the pseudomonas-derived phytotoxins syringomycin and syringopeptin. Regulation of syringomycin and syringopeptin is dependent on the two-component global regulatory system

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