Products for Research Use Only

Araloside A

CAT: 0013-GTR19169370-04Size: 1 ml x 10 mM (in DMSO)Dry Ice: NoHazardous: No
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CAT#:0013-GTR19169370-04Size:1 ml x 10 mM (in DMSO)
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Description
Araloside A (Chikusetsusaponin IV) is a research compound investigated for its potential to modulate the Fas/FasL apoptotic pathway. Studies suggest it may mitigate skin-related apoptotic damage, supporting its use in dermatological research models both in vitro and in vivo.
CAS Number
7518-22-1
Product Name Alternative
Chikusetsusaponin IV, Araloside A, inhibit, Inhibitor, FasL, Fas/FasL, Fas, Renin
Field of Research
Cell Biology, Immunology & Inflammation, Metabolism Research
Purity
99.87% (May vary between batches)
Solubility
10% DMSO+40% PEG300+5% Tween 80+45% Saline:1 mg/mL (1.08 mM) ; DMSO:25 mg/mL (26.97 mM)
Smiles
[H][C@@]1 (O[C@H]2[C@H] (O) [C@@H] (O) [C@] ([H]) (O[C@H]3CC[C@@]4 (C) [C@@] ([H]) (CC[C@]5 (C) [C@]4 ([H]) CC=C4[C@]6 ([H]) CC (C) (C) CC[C@@]6 (CC[C@@]54C) C (=O) O[C@@H]4O[C@H] (CO) [C@@H] (O) [C@H] (O) [C@H]4O) C3 (C) C) O[C@@H]2C (O) =O) O[C@@H] (CO) [C@H] (O) [C@H]1O
Molecular Formula
C47H74O18
Molecular Weight
927.08
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

chikusetsusaponin IV

Chikusetsusaponin-IV is a triterpenoid saponin. It has a role as a metabolite.

CAS Number7518-22-1
PubChem CID10079497
IUPAC Name(2S,3S,4R,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxane-2-carboxylic acid
Molecular FormulaC47H74O18
Molecular Weight927.1
XLogP2.8
Topological Polar Surface Area292
Hydrogen Bond Donor Count10
Hydrogen Bond Acceptor Count18
Rotatable Bond Count10
Heavy Atom Count65
Formal Charge0
Complexity1830
SMILES
C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)C)(C)C)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)C(=O)O)O[C@H]8[C@@H]([C@H]([C@@H](O8)CO)O)O)O)O
InChI
InChI=1S/C47H74O18/c1-42(2)14-16-47(41(59)65-39-33(55)30(52)28(50)23(19-48)61-39)17-15-45(6)21(22(47)18-42)8-9-26-44(5)12-11-27(43(3,4)25(44)10-13-46(26,45)7)62-40-34(56)31(53)35(36(64-40)37(57)58)63-38-32(54)29(51)24(20-49)60-38/h8,22-36,38-40,48-56H,9-20H2,1-7H3,(H,57,58)/t22-,23+,24-,25-,26+,27-,28+,29-,30-,31+,32+,33+,34+,35-,36-,38-,39-,40+,44-,45+,46+,47-/m0/s1
InChIKey
KQSFNXMDCOFFGW-GNDIVNLPSA-N
Chemical Structure
2D Structure
2D structure of chikusetsusaponin IV
CAS: 7518-22-1
CID: 10079497
Formula: C47H74O18
MW: 927.1
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight927.1
XLogP32.8
Hydrogen Bond Donor Count10
Hydrogen Bond Acceptor Count18
Rotatable Bond Count10
Exact Mass926.48751551
Monoisotopic Mass926.48751551
Topological Polar Surface Area292 Ų
Heavy Atom Count65
Formal Charge0
Complexity1830
Isotope Atom Count0
Defined Atom Stereocenter Count22
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes