Revefenacin

Modify Date: 2024-01-09 18:02:09

Revefenacin Structure
Revefenacin structure
Common Name Revefenacin
CAS Number 876296-47-8 Molecular Weight 1048.282
Density 1.2±0.1 g/cm3 Boiling Point 1512.1±65.0 °C at 760 mmHg
Molecular Formula C46H73N13O11S2 Melting Point N/A
MSDS N/A Flash Point 868.3±34.3 °C

 Use of Revefenacin


Selepressin (FE 202158) is a selective vasopressin V1A receptor agonist. Selepressin is a potent vasopressor. Selepressin can be used in the research of septic shock[1][2][4].

 Names

Name SELEPRESSIN
Synonym More Synonyms

 Revefenacin Biological Activity

Description Selepressin (FE 202158) is a selective vasopressin V1A receptor agonist. Selepressin is a potent vasopressor. Selepressin can be used in the research of septic shock[1][2][4].
Related Catalog
In Vitro Selepressin (100 nM, 48 or 72 h) ameliorates thrombin or VEGF-induced HLMVECs barrier dysfunction[3]. Selepressin (1-1000 nM, 72 h) prevents the LPS-Induced loss of VE-cadherin and cortical actin in HLMVECs[3]. Selepressin (100 nM, 48 h) induces the expression of the barrier-protective p53 in HLMVECs[3]. Western Blot Analysis[2] Cell Line: HLMVECs Concentration: 1, 10, 100, 1000 nM Incubation Time: 24 h, 48 h Result: Induced p53 expression levels, but only after treatment of 48 hours at 100 nM.
In Vivo Selepressin (1 μg/kg/min, left jugular vein infusion for 12 min) increases 38.5% of the mean arterial pressure (MAP) in LPS-induced, fluid-resuscitated rabbit endotoxemia model[2]. Selepressin (7 pmol/kg/min, 10 μL/min, i.v. infusion) blocks vascular leak in ovine severe sepsis[4]. Animal Model: LPS-induced, fluid-resuscitated rabbit endotoxemia model[2]. Dosage: 1 μg/kg/min Administration: Left jugular vein infusion for 12 min Result: Decreased mesenteric blood flow (MBF) and increased mesenteric vascular resistance in non-endotoxemic and endotoxemic rabbits.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 1512.1±65.0 °C at 760 mmHg
Molecular Formula C46H73N13O11S2
Molecular Weight 1048.282
Flash Point 868.3±34.3 °C
Exact Mass 1047.499390
LogP -3.83
Vapour Pressure 0.0±0.3 mmHg at 25°C
Index of Refraction 1.545

 Synonyms

Glycinamide, L-cysteinyl-L-phenylalanyl-L-isoleucyl-6-oxo-L-lysyl-L-asparaginyl-L-cysteinyl-L-prolyl-N5-(1-methylethyl)-L-ornithyl-, cyclic (1→6)-disulfide
8P2T76M0SJ
[2-L-phenylalanine,3-L-isoleucine,4-(6-oxo-L-lysine),8-[5-N-(1-methylethyl)-L-ornithine]]human vasopressin
9418
1-({(4R,7S,10S,13S,16S,19R)-19-Amino-10-(4-amino-4-oxobutyl)-7-(2-amino-2-oxoethyl)-16-benzyl-13-[(2S)-2-butanyl]-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaazacycloicosan-4-yl}carbonyl)-L-pro ;lyl-N5-isopropyl-L-ornithylglycinamide
Glycinamide, 1-[[(4R,7S,10S,13S,16S,19R)-19-amino-10-(4-amino-4-oxobutyl)-7-(2-amino-2-oxoethyl)-13-[(1S)-1-methylpropyl]-6,9,12,15,18-pentaoxo-16-(phenylmethyl)-1,2-dithia-5,8,11,14,17-pentaazacycloe ;icos-4-yl]carbonyl]-L-prolyl-N5-(1-methylethyl)-L-ornithyl-
SELEPRESSIN
FE 202158
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