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Ginsenoside Re

Ginsenoside Re structure

CAS No:
52286-59-6
Formula:
C48H82O18
Chemical Name:
Ginsenoside Re
Synonyms:
β-D-Glucopyranoside,(3β,6α,12β)-20-(β-D-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-;(3β,6α,12β)-20-(β-D-Glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside;Ginsenoside Re;Chikusetsusaponin IVc;Ginsenoside B2;Panaxoside Re;Sanchinoside Re;NSC 308877;Notoginsenoside Re;Re ginsenoside;75139-46-7;212055-74-8;324018-82-8;725266-05-7
Categories:
Cosmetic Ingredient > Antioxidant Ingredient

Description

Ginsenoside Re is an extract from Panax notoginseng. Ginsenoside Re decreases the β-amyloid protein (Aβ). Ginsenoside Re plays a role in antiinflammation through inhibition of JNK and NF-κB.

Ginsenoside Re Basic Attributes

Molecular Weight：

947.15

Exact Mass：

947.15

EC Number：

257-814-6

HScode：

29389090

Characteristics

PSA：

298

Density：

1.4±0.1 g/cm3

Melting Point：

200-203 °C

Boiling Point：

1011.8±65.0°C at 760 mmHg

Flash Point：

565.7±34.3 °C

Refractive Index：

1.611

Storage Conditions：

2-8°C

Safety Information

Transport codes：

NONH for all modes of transport

wgk germany：

hazard class code：

20/21/22

safety instructions：

26-36

RTECS Number：

LY9536700

Marks：

GHS Classification：

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 3 companies from 2 notifications to the ECHA C&L Inventory.

Ginsenoside Re Use and Manufacturing

Ginsenoside Re is a protopanaxatriol group saponin, which has various effects in vitro and in vivo, including vasodilation, anti-oxidation, blood lipid lowering and angiogenesis.

Computed Properties

Molecular Weight:947.2
XLogP3:1.6
Hydrogen Bond Donor Count:12
Hydrogen Bond Acceptor Count:18
Rotatable Bond Count:12
Exact Mass:946.55011576
Monoisotopic Mass:946.55011576
Topological Polar Surface Area:298
Heavy Atom Count:66
Complexity:1700
Defined Atom Stereocenter Count:24
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Promotes neural synapse growth and improves cognitive function

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

PRIMA FLEUR HAND SANITIZER LEMON THYME- ethyl alcohol_gel
Manufacturer	Prima Fleur Botanicals, Inc.

THEPURI DEEP PURE HAND SANITIZER- ethyl alcohol_gel
Manufacturer	E.CIS COSMETIC.Co.,Ltd

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Learn More Other Chemicals

Ginsenoside La

123617-34-5
Ginsenoside Rb1

41753-43-9
Ginsenoside K

39262-14-1
Ginsenoside F1 Formula

53963-43-2
Ginsenoside Rh2 Formula

78214-33-2
Ginsenoside Rf Formula

52286-58-5
Ginsenoside Rh4 Structure

174721-08-5
Ginsenoside Rb2 Structure

11021-13-9
What is Ginsenoside Rg2

52286-74-5
What is Ginsenoside Rd

52705-93-8

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Guide of Ginsenoside Re

Description
Basic Attributes
Characteristics
Safety Information
Use and Manufacturing
Computed Properties
Drug Function and Efficacy
Related Drugs
Recommended Suppliers
Learn More Other Chemicals

Ginsenoside Re

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