NNC 55-0396
CAS No. 357400-13-6
NNC 55-0396( NNC 55-0396 dihydrochloride )
Catalog No. M14227 CAS No. 357400-13-6
A potent and selective T-type calcium channel antagonist that blocks recombinant alpha(1)G T-type channels in human embryonic kidney 293 cellswith IC50 of 7 uM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 155 | In Stock |
|
| 5MG | 122 | In Stock |
|
| 10MG | 202 | In Stock |
|
| 25MG | 354 | In Stock |
|
| 50MG | 538 | In Stock |
|
| 100MG | 770 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameNNC 55-0396
-
NoteResearch use only, not for human use.
-
Brief DescriptionA potent and selective T-type calcium channel antagonist that blocks recombinant alpha(1)G T-type channels in human embryonic kidney 293 cellswith IC50 of 7 uM.
-
DescriptionA potent and selective T-type calcium channel antagonist that blocks recombinant alpha(1)G T-type channels in human embryonic kidney 293 cellswith IC50 of 7 uM; has no detectable effect on high-voltage-activated channels in INS-1 cells; inhibits MCF-7 (ERalpha+) cellular proliferation, inhibits tumor-induced angiogenesis in vitro and in vivo by suppressing HIF-1α stability; significantly suppresses glioblastoma tumor growth in a xenograft model.
-
In Vitro——
-
In VivoAnimal Model:GABAA receptor α1 subunit null mouse model Dosage:20 mg/kg Administration:Intraperitoneal injection; 20 mg/kg, once Result:Suppressed tremor in GABAA subunit α1-null mice.
-
SynonymsNNC 55-0396 dihydrochloride
-
PathwayGPCR/G Protein
-
TargetCalcium Channel
-
RecptorCalcium Channel
-
Research AreaCardiovascular Disease
-
Indication——
Chemical Information
-
CAS Number357400-13-6
-
Formula Weight564.5619
-
Molecular FormulaC30H40Cl2FN3O2
-
Purity>98% (HPLC)
-
SolubilityDMSO
-
SMILESCC(C)C1C2=C(CCC1(CCN(C)CCCC3=NC4=CC=CC=C4N3)OC(=O)C5CC5)C=C(C=C2)F.Cl.Cl
-
Chemical NameCyclopropanecarboxylic acid, (1S,2S)-2-[2-[[3-(1H-benzimidazol-2-yl)propyl]methylamino]ethyl]-6-fluoro-1,2,3,4-tetrahydro-1-(1-methylethyl)-2-naphthalenyl ester, hydrochloride (1:2)
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Huang L, et al. J Pharmacol Exp Ther. 2004 Apr;309(1):193-9.
2. Taylor JT, et al. Cancer Lett. 2008 Aug 18;267(1):116-24.
3. Kim KH, et al. J Mol Med (Berl). 2015 May;93(5):499-509.
molnova catalog
related products
-
Diltiazem hydrochlor...
A postsynaptic muscle relaxant that inhibits Ca2+ ions release from sarcoplasmic reticulum stores; antagonizes ryanodine receptors.
-
GV-58
GV-58 is a potent, selective N-Type and P/Q-type Ca2+ Channel agonist with EC50 of 7.2 and 8.8 uM.
-
Azumolene
Azumolene1.EU4093 (azumolene sodium) is a direct acting, skeletal muscle relaxant with structural similarities to dantrolene sodium in that the para-nitro phenyl group of dantrolene sodium is replaced by a para-bromo phenyl group.?2.?The effect of EU4093 on the twitch of the intact rat soleus preparation is nearly maximal at a dose of 20 mg kg-1.?
Cart
sales@molnova.com