[DGlp1,DPhe2,DTrp3,6]-LH-RH structure
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Common Name | [DGlp1,DPhe2,DTrp3,6]-LH-RH | ||
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CAS Number | 68059-94-9 | Molecular Weight | 1321.48000 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C67H84N16O13 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
GHS08 |
Signal Word | Danger |
Use of [DGlp1,DPhe2,DTrp3,6]-LH-RH[D-Glp1,D-Phe2,D-Trp3,6]-LH-RH is a Luteinizing-hormone-releasing hormone (LHRH) analogue. [D-Glp1,D-Phe2,D-Trp3,6]-LH-RH acts as a GnRH receptor antagonist[1]. |
Name | [DGlp1,DPhe2,DTrp3,6]-LH-RH |
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Synonym | More Synonyms |
Description | [D-Glp1,D-Phe2,D-Trp3,6]-LH-RH is a Luteinizing-hormone-releasing hormone (LHRH) analogue. [D-Glp1,D-Phe2,D-Trp3,6]-LH-RH acts as a GnRH receptor antagonist[1]. |
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Related Catalog | |
Target |
GnRH receptor[1] |
In Vitro | [D-Glp1,D-Phe2,D-Trp3,6]-LH-RH (1 μM), together with LH-RH and FSH, blocks the inhibition of FSH-induced steroidogenesis in rat ovary granulosa cells[3]. |
In Vivo | [D-Glp1,D-Phe2,D-Trp3,6]-LH-RH (1.25 and 2.5 mg, subcutaneous injection, b.i.d, for 7 days) prolongs pregnancy in rats[1]. [D-Glp1,D-Phe2,D-Trp3,6]-LH-RH (250 μg) inhibits ovulation by 100% in rats[2]. |
Molecular Formula | C67H84N16O13 |
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Molecular Weight | 1321.48000 |
Exact Mass | 1320.64000 |
PSA | 459.24000 |
LogP | 4.47690 |
Symbol |
GHS08 |
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Signal Word | Danger |
Hazard Statements | H360 |
Precautionary Statements | P201-P308 + P313 |
Personal Protective Equipment | Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
Hazard Codes | T: Toxic; |
Risk Phrases | R60 |
Safety Phrases | 53-22-36/37/39-45 |
RIDADR | NONH for all modes of transport |
Characterization of Leydig cell gonadotropin-releasing hormone binding sites utilizing radiolabeled agonist and antagonist.
Peptides 3(5) , 789-92, (1982) Gonadotropin-releasing hormone (GnRH) binding sites in intact Leydig cells and in membrane preparations were investigated using 125I-labeled GnRH agonist and antagonist. Binding was saturable and invo... |
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Role of lipids in gonadotropin releasing hormone agonists and antagonist binding to rat pituitary.
Biochem. Biophys. Res. Commun. 105(1) , 8-13, (1982) Digestion of pituitary membranes with phospholipase A 2 and phospholipase C abolished, in a dose responsive manner, the specific binding of gonadotropin releasing hormone agonist and antagonist. These... |
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LH-RH analogue acts as substance P antagonist by inhibiting spinal cord vasomotor responses.
Brain Res. 337(2) , 357-61, (1985) Intrathecal injections of the luteinizing hormone-releasing hormone (LH-RH) analogue, [D-pGlu1-D-Phe2-D-Trp3,6]-LH-RH caused dose-dependent decreases in mean arterial blood pressure in anesthetized ra... |
D-pglu1,D-phe2,D-trp3,6-luteinizing*hormone relea |
pglu(1)-phe(2)-trp(3,6)-lhr |
LHRH,pGlu(1)-Phe(2)-Trp(3,6) |
[D-PGLU1,D-PHE2,D-TRP3,6]-LH-RH |
[D-PYR1,D-PHE2,D-TRP3,6]-LH-RH (HUMAN) |
(D-PYR1,D-PHE2,D-TRP3,6)-LHRH |
DGLP-DPHE-DTRP-SER-TYR-DTRP-LEU-ARG-PRO-GLY-NH2 |
[D-PYROGLU1,D-PHE2,D-TRP3,6]-LH-RH |
(D-Pyr1,D-Phe2,D-Trp3 |