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Merck
CN

SML2747

Forsythiaside A

≥98% (HPLC)

Synonym(s):

Forsythoside A, 2-(3,4-Dihydroxyphenyl)ethyl 6-O-(6-deoxy-α-L-mannopyranosyl)-4-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoate]-β-D-glucopyranoside, Forsythiaside

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About This Item

Empirical Formula (Hill Notation):
C29H36O15
CAS Number:
Molecular Weight:
624.59
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
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Quality Segment

assay

≥98% (HPLC)

form

powder

optical activity

[α]/D -25 to -17°, c = 1 in methanol

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

−20°C

SMILES string

O1[C@H]([C@@H]([C@H]([C@@H]([C@H]1CO[C@@H]4O[C@H]([C@@H]([C@H]([C@H]4O)O)O)C)OC(=O)\C=C\c3cc(c(cc3)O)O)O)O)OCCc2cc(c(cc2)O)O

InChI

1S/C29H36O15/c1-13-22(35)23(36)25(38)29(42-13)41-12-20-27(44-21(34)7-4-14-2-5-16(30)18(32)10-14)24(37)26(39)28(43-20)40-9-8-15-3-6-17(31)19(33)11-15/h2-7,10-11,13,20,22-33,35-39H,8-9,12H2,1H3/b7-4+/t13-,20+,22-,23+,24+,25+,26+,27+,28+,29+/m0/s1

InChI key

DTOUWTJYUCZJQD-UJERWXFOSA-N

Biochem/physiol Actions

Forsythiaside A is a most abundant phenylethanoid glycosides isolated from Forsythia suspense that exhibits anti-inflammatory and neuroprotective activities. It appears that forsythoside A exerts antipyretic activities through inhibition of transient receptor potential vanilloid 1 (TRPV1) channel.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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