
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 508-75-8 |
| Catalog No. | 2A-9009909 |
| Chinese Name | K-毒毛旋花子配质-3-L-鼠李糖甙 |
| Synonyms | CONVALLATOXIN; Convallatoxin |
| Molecular Formula | C29H42O10 |
| Molecular Weight | 550.64 |
| Purity | 90 |
| Density | 1.41 g/cm3 |
| Boiling Point | 757.3ºC at 760 mmHg |
| Melting Point | 235-242ºC |
| Appearance | powder |
| Storage Condition | 2-8℃, dry |
| Packaging | III |
| Application | Convallatoxin is a cardiac glycoside isolated from Adonis amurensis Regel et Radde. Convallatoxin improves colitis through activation of PPARγ and inhibition of NF-κB. Convallatoxin is a P-glycoprotei |
| EINECS | 208-086-3 |
| PubChem ID | 24893136 |
| MDL Number | MFCD00069477 |
| SMILES | C[C@@H]1O[C@@H](O[C@H]2CC[C@]3(C=O)[C@H]4CC[C@]5(C)[C@H](CC[C@]5(O)[C@@H]4CC[C@]3(O)C2)C6=CC(=O)OC6)[C@H](O)[C@H](O)[C@H]1O |
| InChI | 1S/C29H42O10/c1-15-22(32)23(33)24(34)25(38-15)39-17-3-8-27(14-30)19-4-7-26(2)18(16-11-21(31)37-13-16)6-10-29(26,36)20(19)5-9-28(27,35)12-17/h11,14-15,17-20,22-25,32-36H,3-10,12-13H2,1-2H3/t15-,17-,18+,19-,20+,22-,23+,24+,25-,26+,27-,28-,29-/m0/s1 |
| InChI Key | HULMNSIAKWANQO-JQKSAQOKSA-N |
| NACRES Code | NA.77 |
| UNSPSC | 12352200 |
| Hazard Symbols | 6.1(b) |
| MSDS | msds/9909_1_508_75_8.pdf |
| Bioactivity | Convallatoxin is a cardiac glycoside isolated from Adonis amurensis Regel et Radde. Convallatoxin ameliorates colitic inflammation via activation of PPARγ and suppression of NF-κB. Convallatoxin is a P-glycoprotein (P-gp) substrate and recognized Val982 as an important amino acid involved in its transport. Convallatoxin is an enhancer of ligand-induced MOR endocytosis with high potency and efficacy. Anti-inflammatory and anti-proliferative properties[1][2][3]. Related Catalog Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> PPAR Research Areas >> Inflammation/Immunology Signaling Pathways >> Membrane Transporter/Ion Channel >> P-glycoprotein In Vitro Convallatoxin induces HaCaT cell necroptosis[4]. In Vivo Convallatoxin exerts antipsoriatic activities in two mouse models of psoriasis[4]. References [1]. Li MY, et al. Convallatoxin protects against dextran sulfate sodium-induced experimental colitis in mice by inhibiting NF-κB signaling through activation of PPARγ. Pharmacol Res. 2019 Sep;147:104355. [2]. Gozalpour E, et al. Convallatoxin: a new P-glycoprotein substrate. Eur J Pharmacol. 2014 Dec 5;744:18-27. [3]. Chao PK, et al. Convallatoxin enhance the ligand-induced mu-opioid receptor endocytosis and attenuate morphine antinociceptive tolerance in mice. Sci Rep. 2019 Feb 20;9(1):2405. [4]. Jiang BW, et al. Convallatoxin induces HaCaT cell necroptosis and ameliorates skin lesions in psoriasis-like mouse models. Biomed Pharmacother. 2020 Jan;121:109615. Chemical & Physical Properties Density 1.41 g/cm3 Boiling Point 757.3ºC at 760 mmHg Melting Point 235-242ºC Molecular Formula C29H42O10 Molecular Weight 550.63800 Flash Point 247.1ºC Exact Mass 550.27800 PSA 162.98000 LogP 0.75000 Index of Refraction 1.622 InChIKey HULMNSIAKWANQO-JQKSAQOKSA-N SMILES CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O)C2)C(O)C(O)C1O |
| Use of | Convallatoxin is a cardiac glycoside isolated from Adonis amurensis Regel et Radde. Convallatoxin ameliorates colitic inflammation via activation of PPARγ and suppression of NF-κB. Convallatoxin is a P-glycoprotein (P-gp) substrate and recognized Val982 as an important amino acid involved in its transport. Convallatoxin is an enhancer of ligand-induced MOR endocytosis with high potency and efficacy. Anti-inflammatory and anti-proliferative properties[1][2][3]. Properties Articles29 Name convallatoxin Synonym More Synonyms CONVALLATOXIN Biological Activity Description Convallatoxin is a cardiac glycoside isolated from Adonis amurensis Regel et Radde. Convallatoxin ameliorates colitic inflammation via activation of PPARγ and suppression of NF-κB. Convallatoxin is a P-glycoprotein (P-gp) substrate and recognized Val982 as an important amino acid involved in its transport. Convallatoxin is an enhancer of ligand-induced MOR endocytosis with high potency and efficacy. Anti-inflammatory and anti-proliferative properties[1][2][3]. Related Catalog Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> PPAR Research Areas >> Inflammation/Immunology Signaling Pathways >> Membrane Transporter/Ion Channel >> P-glycoprotein In Vitro Convallatoxin induces HaCaT cell necroptosis[4]. In Vivo Convallatoxin exerts antipsoriatic activities in two mouse models of psoriasis[4]. References [1]. Li MY, et al. Convallatoxin protects against dextran sulfate sodium-induced experimental colitis in mice by inhibiting NF-κB signaling through activation of PPARγ. Pharmacol Res. 2019 Sep;147:104355. [2]. Gozalpour E, et al. Convallatoxin: a new P-glycoprotein substrate. Eur J Pharmacol. 2014 Dec 5;744:18-27. [3]. Chao PK, et al. Convallatoxin enhance the ligand-induced mu-opioid receptor endocytosis and attenuate morphine antinociceptive tolerance in mice. Sci Rep. 2019 Feb 20;9(1):2405. [4]. Jiang BW, et al. Convallatoxin induces HaCaT cell necroptosis and ameliorates skin lesions in psoriasis-like mouse models. Biomed Pharmacother. 2020 Jan;121:109615. Chemical & Physical Properties Molecular Formula C29H42O10 Exact Mass 550.27800 PSA 162.98000 LogP 0.75000 Index of Refraction 1.622 InChIKey HULMNSIAKWANQO-JQKSAQOKSA-N |
| Transport Info | Product name: lily of the valley toxin |
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