Fedovapagon

    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 319788

CAS#: 347887-36-9

Description: Fedovapagon, also known as VA106483 and VT483, is a potent, nonpeptidic vasopressin V2 receptor agonist. Vasopressin (AVP) is a hormone that stimulates an increase in water permeability through activation of V2 receptors in the kidney.


Chemical Structure

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Fedovapagon
CAS# 347887-36-9

Theoretical Analysis

MedKoo Cat#: 319788
Name: Fedovapagon
CAS#: 347887-36-9
Chemical Formula: C27H34N4O3
Exact Mass: 462.26
Molecular Weight: 462.594
Elemental Analysis: C, 70.10; H, 7.41; N, 12.11; O, 10.38

Price and Availability

Size Price Availability Quantity
10mg USD -2
25mg USD -2
50mg USD -2
100mg USD -2
200mg USD -2
500mg USD -2
1g USD -1
2g USD -1
5g USD -1
10g USD -1
20g USD -1
50g USD -1
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Synonym: VA106483; VA-106483; VA 106483; VT483; VT-483; VT 483; Fedovapagon

IUPAC/Chemical Name: (S)-N2,N2-dimethyl-N1-(2-methyl-4-(2,3,4,5-tetrahydro-1H-benzo[b]azepine-1-carbonyl)benzyl)pyrrolidine-1,2-dicarboxamide

InChi Key: RUOLFWZIFNQQGH-DEOSSOPVSA-N

InChi Code: InChI=1S/C27H34N4O3/c1-19-17-21(25(32)30-15-7-6-10-20-9-4-5-11-23(20)30)13-14-22(19)18-28-27(34)31-16-8-12-24(31)26(33)29(2)3/h4-5,9,11,13-14,17,24H,6-8,10,12,15-16,18H2,1-3H3,(H,28,34)/t24-/m0/s1

SMILES Code: O=C(N1[C@H](C(N(C)C)=O)CCC1)NCC2=CC=C(C(N3CCCCC4=CC=CC=C43)=O)C=C2C

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO, not in water

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 462.59 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Yea CM, Allan CE, Ashworth DM, Barnett J, Baxter AJ, Broadbridge JD, Franklin
RJ, Hampton SL, Hudson P, Horton JA, Jenkins PD, Penson AM, Pitt GR, Rivière P,
Robson PA, Rooker DP, Semple G, Sheppard A, Haigh RM, Roe MB. New benzylureas as
a novel series of potent, nonpeptidic vasopressin V2 receptor agonists. J Med
Chem. 2008 Dec 25;51(24):8124-34. doi: 10.1021/jm8008162. PubMed PMID: 19053774.