Carbazochrome sodium sulfonate
CAS No. 51460-26-5
Carbazochrome sodium sulfonate( AC17 | 4arylidene curcumin | )
Catalog No. M14783 CAS No. 51460-26-5
Carbazochrome sodium sulfonate (AC-17) is an antihemorrhagic for use in the treatment of hemorrhoids.
Carbazochrome sodium sulfonate (AC-17) is an antihemorrhagic for use in the treatment of hemorrhoids.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
25MG | 27 | In Stock |
|
50MG | 53 | In Stock |
|
100MG | 87 | In Stock |
|
200MG | Get Quote | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameCarbazochrome sodium sulfonate
-
NoteResearch use only, not for human use.
-
Brief DescriptionCarbazochrome sodium sulfonate (AC-17) is an antihemorrhagic for use in the treatment of hemorrhoids.
-
DescriptionCarbazochrome sodium sulfonate (AC-17) is an antihemorrhagic for use in the treatment of hemorrhoids(In Vitro):Carbazochrome (0.1-10 μM) inhibits the Bradykinin induced and thrombin-induced formation of [3H]IP3 in a concentration-dependent manner. Carbazochrome (0.1-1 μM), when included from 30 min before stimulation, significantly suppressed the enhancement of permeability induced by vasoactive substances.(In Vivo):Carbazochrome inhibits the severe pulmonary dysfunction induced by the intravenous injection of radiographic contrast media. Carbazochrome (1-10 mg/kg, i.v.) attenuates pulmonary dysfunction induced by a radiographic contrast medium in rats.
-
In VitroCarbazochrome (0.1-10 μM) inhibits the Bradykinin induced and thrombin-induced formation of [3H]IP3in a concentration-dependent manner.Carbazochrome (0.1-1 μM), when included from 30 min before stimulation, significantly suppressed the enhancement of permeability induced by vasoactive substances.
-
In VivoCarbazochrome inhibits the severe pulmonary dysfunction induced by the intravenous injection of radiographic contrast media. Carbazochrome (1-10 mg/kg, i.v.) attenuates pulmonary dysfunction induced by a radiographic contrast medium in rats. Animal Model:Male Sprague-Dawley rats weighing 180-230 g Dosage:1, 5 and 10 mg/kg Administration:I.v.; injected 30, 60, or 90 min before Ioxaglate injection (4 g I/kg, i.v.).Result:Attenuated the Ioxaglate-increased vascular permeability at the dose of 1, 5 and 10 mg/kg in a dose-dependent manner, achieving statistical significance at 5 and 10 mg/kg.
-
SynonymsAC17 | 4arylidene curcumin |
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research AreaCardiovascular Disease
-
Indication——
Chemical Information
-
CAS Number51460-26-5
-
Formula Weight376.32
-
Molecular FormulaC10H17N4NaO8S
-
Purity>98% (HPLC)
-
SolubilityWater: 3 mg/mL (9.3 mM); DMSO: 64 mg/mL (198.59 mM)
-
SMILESO=C(/C(C(/C=C/C1=CC=C(OC)C(OC)=C1)=O)=C/C2=CC=C(O)C(OC)=C2)/C=C/C3=CC=C(OC)C(OC)=C3
-
Chemical Name(1E,6E)-1,7-bis(3,4-dimethoxyphenyl)-4-(4-hydroxy-3-methoxybenzylidene)hepta-1,6-diene-3,5-dione
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Sendo T, et al. Naunyn Schmiedebergs Arch Pharmacol, 2003, 368(3), 175-180.
molnova catalog
related products
-
(3,4-Dihydroxyphenyl...
The herbs of Gastrodia elata BL.
-
Benzododecinium chlo...
Benzyldimethyldodecylammonium chloride is a quaternary ammonium compound.Benzododecinium chloride is an irritant for eye.
-
6-Hydroxykaempferol ...
6-Hydroxykaempferol 3-beta-rutinoside is a natural product.