Bufalin
Cat.No:IB0300 Solarbio
CAS:465-21-4
Molecular Formula:C24H34O4
Molecular Weight:386.53
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:White to off-white Solid
Qty:
Size:
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BufalinCAS:465-21-4
Molecular Formula:C24H34O4
Molecular Weight:386.53
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:White to off-white Solid
Qty:
Size:
CAS | 465-21-4 |
Name | Bufalin |
Molecular Formula | C24H34O4 |
Molecular Weight | 386.53 |
Solubility | Soluble in DMSO |
Purity | HPLC≥98% |
Appearance | White to off-white Solid |
Storage | Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year |
MDL | MFCD00056525 |
SMILES | O[C@]([C@@](CC[C@@]1([H])[C@@]2(CC[C@H](O)C1)C)([H])[C@]2([H])CC3)(CC[C@@H]4C(C=C5)=COC5=O)[C@]34C |
InChIKey | QEEBRPGZBVVINN-BMPKRDENSA-N |
InChI | InChI=1S/C24H34O4/c1-22-10-7-17(25)13-16(22)4-5-20-19(22)8-11-23(2)18(9-12-24(20,23)27)15-3-6-21(26)28-14-15/h3,6,14,16-20,25,27H,4-5,7-13H2,1-2H3/t16-,17+,18-,19+,20-,22+,23-,24+/m1/s1 |
PubChem CID | 9547215 |
Target Point | Na+/K+ ATPase |
Passage | Membrane Transporter&Ion Channel |
Background | Bufalin, an immunoactive component of toad venom, is a potent Na+/K+-ATPase inhibitor that binds to the subunits α1, α2 and α3 of Na+/K+-ATPase, α1, α2 and α3. |
Unit | Bottle |
Specification | 5mg 10mM*1mL in DMSO 10mg |
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
Note:
1. The products are all for scientific research use only. Do not use it for medical, clinical diagnosis or treatment, food and cosmetics, etc. Do not store them in ordinary residential areas.
2. For your safety and health, please wear laboratory clothes, disposable gloves and masks.
3. The experimental results may be affected by many factors, after-sale service is limited to the product itself and does not involve other compensation.
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Bufalin reduces myocardial infarction-induced myocardial fibrosis and improves cardiac function by inhibiting the NLRP3/IL-1β signalling pathway
Click to check >>Author:Xiang Wei; Yang Lv; Chenxi Yang; Rifeng Gao; Su Zo
IF:2.9630
Publish_to:CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY
PMID:37243403