Cart
sales@molnova.com
Dihydrocatalpol
CAS No. 6736-86-3
Dihydrocatalpol( (2S,3R,4S,5S,6R)-2-[[(1aS,1bS,2S,5aR,6S,6aS)-6-hydroxy-1a-(hydroxymethyl)-2,4,5,5a,6,6a-hexahydro-1bH-oxireno[5,6]cyclopenta[1,3-c]pyran-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol )
Catalog No. M24684 CAS No. 6736-86-3
Dihydrocatalpol,a natural product obtained from the herbs of Rehmannia glutinosa.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 342 | In Stock |
|
| 10MG | 509 | In Stock |
|
| 25MG | 801 | In Stock |
|
| 50MG | 1107 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameDihydrocatalpol
-
NoteResearch use only, not for human use.
-
Brief DescriptionDihydrocatalpol,a natural product obtained from the herbs of Rehmannia glutinosa.
-
DescriptionDihydrocatalpol,a natural product obtained from the herbs of Rehmannia glutinosa.
-
In Vitro——
-
In Vivo——
-
Synonyms(2S,3R,4S,5S,6R)-2-[[(1aS,1bS,2S,5aR,6S,6aS)-6-hydroxy-1a-(hydroxymethyl)-2,4,5,5a,6,6a-hexahydro-1bH-oxireno[5,6]cyclopenta[1,3-c]pyran-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number6736-86-3
-
Formula Weight364.35
-
Molecular FormulaC15H24O10
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO[C@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)[C@@H]1O[C@H]2[C@@]3([H])C([C@H](O)[C@@]4([H])[C@]3(CO)O4)CCO2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
Pachypodol
Pachypodol has antibacterial and antifungal activities against Bacillus subtilis, Staphylococcus aureus, Staphylococcus faecalis, Echerichia coli, Pseudomonas aeruginosa, Candida albicans, Candida krusei and Candida galabrata.
-
Caraganaphenol A
Caraganaphenol A is a natural product for research related to life sciences.
-
ELA-32 (human)
Potent, high affinity apelin receptor agonist (IC50 = 0.27 nM; Kd = 0.51 nM). Exhibits no binding GPR15 and GPR25. Activates the PI3K/AKT pathway and promotes self-renewal of hESCs via cell-cycle progression and protein translation. Also potentiates the TGFβ pathway, priming hESCs toward the endoderm lineage. Stimulates angiogenesis in HUVEC cells. Relaxes mouse aortic vessels. Functions as an anorexigenic hormone through activation of the AVP and CRH neurons in the PVN.
