851671
Helicin
99%
Synonym(s):
Salicylaldehyde β-D-glucoside
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About This Item
Empirical Formula (Hill Notation):
C13H16O7
CAS Number:
Molecular Weight:
284.26
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
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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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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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