Rubrofusarin-6-O-beta-D-gentiobioside
CAS No. 24577-90-0
Rubrofusarin-6-O-beta-D-gentiobioside( —— )
Catalog No. M24129 CAS No. 24577-90-0
Rubrofusarin-6-O-beta-D-gentiobioside can significantly decrease the expression of TGF-beta1 and fibronectin and NF-kappaB DNA binding activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 176 | In Stock |
|
| 10MG | 266 | In Stock |
|
| 25MG | 447 | In Stock |
|
| 50MG | 651 | In Stock |
|
| 100MG | 888 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameRubrofusarin-6-O-beta-D-gentiobioside
-
NoteResearch use only, not for human use.
-
Brief DescriptionRubrofusarin-6-O-beta-D-gentiobioside can significantly decrease the expression of TGF-beta1 and fibronectin and NF-kappaB DNA binding activity.
-
DescriptionRubrofusarin-6-O-beta-D-gentiobioside can significantly decrease the expression of TGF-beta1 and fibronectin and NF-kappaB DNA binding activity, suggests that it has potential as a preventive agent for advanced glycation end products-related diabetic complications.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayTGF-beta/Smad
-
TargetTGFBR
-
RecptorTGFβ|NF-κB|ERK
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number24577-90-0
-
Formula Weight596.5
-
Molecular FormulaC27H32O15
-
Purity>98% (HPLC)
-
SolubilityDMSO:10 mM
-
SMILESOC1=C2C(O[C@@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)CO[C@@H]4O[C@@H]([C@@H](O)[C@H](O)[C@H]4O)CO)=CC(OC)=CC2=CC5=C1C(C=C(C)O5)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Extract of Cassiae Semen and its major compound inhibit S100b-induced TGF-beta1 and fibronectin expression in mouse glomerular mesangial cells.Eur J Pharmacol. 2010 Sep 1;641(1):7-14.
molnova catalog
related products
-
JL5
JL5 is a novel potent, selective BMP receptor inhibitor with IC50 of 1, <5 and 2 nM for ALK2/ACVR1, ALK3/BMPR1A and ALK6/BMPR1B, respectively.
-
AZ12601011
AZ12601011 (AZ-12601011) is a potent, selective inhibitor of ALK4, ALK7 and TGFBR1 (Kd=2.9 nM).
-
VU 0469381
A potent, sellective BMP receptor ALK2 antaognist with Ki of 32 nM, with no affinity for ALK3/4/5/6.
Cart
sales@molnova.com