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Ginsenoside F1 - 96%, high purity , CAS No.53963-43-2

COA COA
    Grade & Purity:
  • ≥96%
In stock
Item Number
G170877
Grouped product items
SKU Size
Availability
 Price Qty
G170877-5mg
5mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$68.90
G170877-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$117.90
G170877-25mg
25mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$265.90
G170877-50mg
50mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$355.90
G170877-100mg
100mg
2
$640.90
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Bulk Order  SDS  DATASHEET  Specification Sheet

Triterpenoid saponin

View related series
Cytochrome P450 (241) Endogenous Metabolite (959) Lipid metabolism (1912) Metabolic Enzyme/Protease (4860) Metabolite (5307)

Basic Description

Synonyms 20(S)-ginsenoside F1 | Q-100611 | AS-76768 | Ginsenoside F1 | (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(2S)-6-methyl-2-[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,6,12-trihydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]p
Specifications & Purity ≥96%
Biochemical and Physiological Mechanisms Triterpenoid saponin. Enzymatically modified derivative of ginsenoside Rg 1 . Protects against UVB-induced apoptosis in vitro . Active in vitro and in vivo .
Storage Temp Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Lipids and lipid-like molecules
Class Prenol lipids
Subclass Terpene glycosides
Intermediate Tree Nodes Triterpene glycosides
Direct Parent Triterpene saponins
Alternative Parents Triterpenoids  12-hydroxysteroids  14-alpha-methylsteroids  3-beta-hydroxysteroids  6-hydroxysteroids  Fatty acyl glycosides of mono- and disaccharides  Alkyl glycosides  O-glycosyl compounds  Oxanes  Monosaccharides  Secondary alcohols  Cyclic alcohols and derivatives  Polyols  Oxacyclic compounds  Acetals  Hydrocarbon derivatives  Primary alcohols  
Molecular Framework Aliphatic heteropolycyclic compounds
Substituents Triterpene saponin - Triterpenoid - 3-hydroxysteroid - 14-alpha-methylsteroid - 12-hydroxysteroid - 6-hydroxysteroid - Hydroxysteroid - 3-beta-hydroxysteroid - Steroid - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Glycosyl compound - O-glycosyl compound - Monosaccharide - Fatty acyl - Oxane - Cyclic alcohol - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Acetal - Polyol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Primary alcohol - Alcohol - Aliphatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.
External Descriptors 3beta-hydroxy steroid - beta-D-glucoside - 6alpha-hydroxy steroid - tetracyclic triterpenoid - 12beta-hydroxy steroid - ginsenoside

Associated Targets(Human)

HL-60 (67320 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
U-251 (51189 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HaCaT (4069 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

C6 (2371 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(2S)-6-methyl-2-[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,6,12-trihydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]hept-5-en-2-yl]oxyoxane-3,4,5-triol
INCHI InChI=1S/C36H62O9/c1-19(2)10-9-13-36(8,45-31-29(43)28(42)27(41)23(18-37)44-31)20-11-15-34(6)26(20)21(38)16-24-33(5)14-12-25(40)32(3,4)30(33)22(39)17-35(24,34)7/h10,20-31,37-43H,9,11-18H2,1-8H3/t20-,21+,22-,23+,24+,25-,26-,27+,28-,29+,30-,31-,33+,34+,35+,36-/m0/s1
InChIKey XNGXWSFSJIQMNC-FIYORUNESA-N
Smiles CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CC(C4C3(CCC(C4(C)C)O)C)O)C)O)C)OC5C(C(C(C(O5)CO)O)O)O)C
Isomeric SMILES CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(C[C@@H]([C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)O)C)O)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)C
Molecular Weight 638.87
Reaxy-Rn 42218136
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=42218136&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot Number Certificate Type Date Item
J2115176 Certificate of Analysis Jul 15, 2024 G170877
J2115208 Certificate of Analysis Jul 15, 2024 G170877
J2115229 Certificate of Analysis Jul 15, 2024 G170877
J2115250 Certificate of Analysis Jul 15, 2024 G170877
J2115259 Certificate of Analysis Jul 15, 2024 G170877

Chemical and Physical Properties

Solubility DMSO (Slightly), Methanol (Slightly)
Sensitivity Moisture sensitive
Molecular Weight 638.900 g/mol
XLogP3 4.300
Hydrogen Bond Donor Count 7
Hydrogen Bond Acceptor Count 9
Rotatable Bond Count 7
Exact Mass 638.439 Da
Monoisotopic Mass 638.439 Da
Topological Polar Surface Area 160.000 Ų
Heavy Atom Count 45
Formal Charge 0
Complexity 1110.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 16
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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