3-O-Caffeoyl-betulin
| Code | Size | Price |
|---|
| BVT-0393-M001 | 1 mg | £95.00 |
Quantity:
| BVT-0393-M005 | 5 mg | £350.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
-20°C
Documents
Further Information
Alternate Names/Synonyms:
Betulin 3-caffeate
Appearance:
Light yellow solid.
CAS:
89130-86-9
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.
Hazards:
H302
InChi:
InChI=1S/C39H56O5/c1-24(2)26-14-19-39(23-40)21-20-37(6)27(34(26)39)10-12-31-36(5)17-16-32(35(3,4)30(36)15-18-38(31,37)7)44-33(43)13-9-25-8-11-28(41)29(42)22-25/h8-9,11,13,22,26-27,30-32,34,40-42H,1,10,12,14-21,23H2,2-7H3/b13-9+/t26-,27+,30-,31+,32-,34+,36-,37+,38+,39+/m0/s1
InChiKey:
VOQSZICWRNPAMF-IUGYEWCASA-N
Long Description:
Chemical. CAS: 89130-86-9. Formula: C39H56O5. MW: 604.9. Isolated from birch bark (Betula alba). Anti-proliferative. Shows anti-melanoma activity. Sun-block ingredient for cosmetics. Prevents sun burning, premature aging and skin cancer. Antibacterial.
MDL:
MFCD17214892
Molecular Formula:
C39H56O5
Molecular Weight:
604.9
Package Type:
Plastic Vial
Precautions:
P264, P301, P312, P330
Product Description:
Anti-proliferative. Shows anti-melanoma activity. Sun-block ingredient for cosmetics. Prevents sun burning, premature aging and skin cancer. Antibacterial.
Purity:
>96% (HPLC)
Signal word:
Warning
SMILES:
[H][C@]12[C@@H](CC[C@]1(CO)CC[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OC(=O)C=CC4=CC(O)=C(O)C=C4)C(C)(C)[C@]3([H])CC[C@@]12C)C(C)=C
Solubility Chemicals:
Soluble in methanol, acetone or DMSO.
Source / Host:
Isolated from birch bark (Betula alba).
Transportation:
Non-hazardous
UNSPSC Category:
Natural Products/Extracts
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 1 year after receipt when stored at -20°C. After reconstitution protect from light at -20°C.
References
Betulin-3-caffeate from Quercus suber. 13C-NMR spectra of some lupenes: A. Patra, et al.; J. Nat. Prod. 51, 217 (1988) | Triterpene caffeates from bark of Betula pubescens: H. Pan, et al.; Phytochem. 37, 795 (1994) | Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 epidermal cells: H. Gao, et al.; Chem. Pharm. Bull. 51, 1318 (2003) | Antibacterial activity of hydrolyzable tannins derived from medicinal plants against helicobacter pylori: K. Funatogawa, et al.; Microbiol. Immunol. 48, 251 (2004) | Birch bark research and development: P. A. Krasutsky; Nat. Prod. Rep. 23, 919 (2006)
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