Neuropeptide VF (124-131) (human) trifluoroacetate salt structure
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Common Name | Neuropeptide VF (124-131) (human) trifluoroacetate salt | ||
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CAS Number | 311309-27-0 | Molecular Weight | 969.14100 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C45H72N14O10 | Melting Point | N/A | |
MSDS | USA | Flash Point | N/A |
Use of Neuropeptide VF (124-131) (human) trifluoroacetate saltRFRP-3 (Neuropeptide VF(124-131))(human), a human GnIH peptide homolog, is a potent inhibitor of gonadotropin secretion by inhibiting Ca2+ mobilization. RFRP-3(human) is a NPFF1 receptor agonist, it inhibits forskolin-induced production of cAMP with an IC50 of 0.7 nM[1]. |
Name | h-val-pro-asn-leu-pro-gln-arg-phe-nh2 |
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Synonym | More Synonyms |
Description | RFRP-3 (Neuropeptide VF(124-131))(human), a human GnIH peptide homolog, is a potent inhibitor of gonadotropin secretion by inhibiting Ca2+ mobilization. RFRP-3(human) is a NPFF1 receptor agonist, it inhibits forskolin-induced production of cAMP with an IC50 of 0.7 nM[1]. |
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Related Catalog | |
In Vitro | RFRP-3 efficiently inhibits forskolin-induced production of cAMP with an IC50 of 0.7 nM[1]. Scatchard-plot analysis shows that 125I-labelled hRFRP-3 has a single class of high-affinity binding sites for the membrane fractions of CHO cells expressing rat OT7T022, the Kd value and the Bmax values are 0.19 nM and 1.3 pM, respectively. RFRP-3 specifically stimulate cells transfected with a new orphan 7TMR, OT7T022, it binds to OT7T022 as a specific ligand with high affinity (Kd= 0.19 nM)[1]. RFRP-3 (10-8 to 10-14M) has no effect on LH and FSH levels alone, but when it combines with GnRH, LH and FSH secretion is significantly reduced by the combination[1]. |
References |
Molecular Formula | C45H72N14O10 |
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Molecular Weight | 969.14100 |
Exact Mass | 968.55600 |
PSA | 403.31000 |
LogP | 2.37640 |
Hazard Codes | Xi |
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RFRP-3 human trifluoroacetate salt |
H2N-VPNLPQRF-AMIDE |
V-8-F-NH2,NPVF |
NPVF |
V-8-F-NH2 |
Neuropeptide VF (124-131) (human) |