Cart
sales@molnova.com
Annaosanchun
CAS No. 4725-51-3
Annaosanchun( YC-6 | YC 6 | YC6 )
Catalog No. M27122 CAS No. 4725-51-3
Annaosanchun(YC-6) is potentially for the treatment of acute ischemic stroke (AIS).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 93 | In Stock |
|
| 5MG | 85 | In Stock |
|
| 10MG | 136 | In Stock |
|
| 25MG | 226 | In Stock |
|
| 50MG | 332 | 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 NameAnnaosanchun
-
NoteResearch use only, not for human use.
-
Brief DescriptionAnnaosanchun(YC-6) is potentially for the treatment of acute ischemic stroke (AIS).
-
DescriptionAnnaosanchun(YC-6) is potentially for the treatment of acute ischemic stroke (AIS).
-
In Vitro——
-
In Vivo——
-
SynonymsYC-6 | YC 6 | YC6
-
PathwayOthers
-
TargetOther Targets
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number4725-51-3
-
Formula Weight308.462
-
Molecular FormulaC19H32O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILES[H][C@@]12CCC[C@@]1(C)CC[C@@]1([H])[C@@]2([H])C[C@@H](O)[C@@]2(O)C[C@@H](O)CC[C@]12C
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Uddin SJ, Grice D, Tiralongo E. Evaluation of cytotoxic activity of patriscabratine, tetracosane and various flavonoids isolated from the Bangladeshi medicinal plant Acrostichum aureum. Pharm Biol. 2012 Oct;50(10):1276-80.
molnova catalog
related products
-
Ambradiolic acid 3-O...
Ambradiolic acid 3-O-α-L-arabinopyranosyl-28-β-D-glucopyranosyl(1→6)-β-D-glucopyranoside
-
HLM006474
HLM006474 is a pan inhibitor of E2F. This inhibits E2F4 DNA-binding (IC50: 29.8 μM in A375 cells).HLM006474 causes the viability of both SCLC and NSCLC lines (IC50 ranging from 15 to 75 μM). HLM006474 displays little activities against E2F4 DNA-binding in A375 cells at 10 and 20 μM, apparently inhibits E2F4 DNA-binding at 40 μM, and increasingly suppresses the effect at 60 and 80 μM concentrations.
-
Insulin Receptor (11...
Insulin Receptor (1142-1153)
