Balovaptan
CAS No. 1228088-30-9
Balovaptan( RG7314 )
Catalog No. M23402 CAS No. 1228088-30-9
Balovaptan is a highly potent and selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 54 | In Stock |
|
| 10MG | 87 | In Stock |
|
| 25MG | 177 | In Stock |
|
| 50MG | 286 | In Stock |
|
| 100MG | 447 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameBalovaptan
-
NoteResearch use only, not for human use.
-
Brief DescriptionBalovaptan is a highly potent and selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist.
-
DescriptionBalovaptan is a highly potent and selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist, with Kis of 1 and 39 nM for human (hV1a) and mouse (mV1a) receptors. It is used for the research of autism.
-
In VitroBalovaptan (RG7314) shows >30000-fold selectivity for hV1a over hV2 receptors, 9891-fold selectivity over hOTR (human oxytocin receptor).
-
In Vivo——
-
SynonymsRG7314
-
PathwayGPCR/G Protein
-
TargetVasopressin Receptor
-
Recptorvasopressin receptor 1a
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1228088-30-9
-
Formula Weight409.91
-
Molecular FormulaC22H24ClN5O
-
Purity>98% (HPLC)
-
SolubilityDMSO:62.5 mg/mL (152.47 mM; Need ultrasonic)
-
SMILESCN1Cc(cc(cc2)Cl)c2-n2c(C(CC3)CCC3Oc3ncccc3)nnc2C1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Ratni H, et al. Discovery of highly selective brain-penetrant vasopressin 1a antagonists for the potential treatment of autism via a chemogenomic and scaffold hopping approach. J Med Chem. 2015 Mar 12;58(5):2275-89.
molnova catalog
related products
-
Conivaptan hydrochlo...
Conivaptan (YM-087)?is a potent, selective nonpeptide vasopressin V1A and V2 receptor antagonist with Ki of 0.48 nM and 3.04 nM respectively.
-
(d(CH2)51,Tyr(Me)2,A...
Selective vasopressin V1A receptor antagonist. Inhibits vasopressin and oxytocin-induced increases in intracellular calcium concentrations in vitro (IC50 values are 5 and 30 nM respectively). Exhibits potent and prolonged antivasopressor activity and induces anxiolytic-like effects in the dorsal, but not ventral, hippocampus in vivo.
-
E-4177
E-4177 is an angiotensin II type 1 receptor (AT1R) antagonist and can be used to study cardiovascular diseases.
Cart
sales@molnova.com