RP 67580
Modify Date: 2024-03-08 23:01:19
RP 67580 structure
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Common Name | RP 67580 | ||
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| CAS Number | 135911-02-3 | Molecular Weight | 438.56 | |
| Density | 1.17 g/cm3 | Boiling Point | 588.5ºC at 760 mmHg | |
| Molecular Formula | C29H30N2O2 | Melting Point | 195-188ºC | |
| MSDS | N/A | Flash Point | 309.7ºC | |
Use of RP 67580RP 67580 is a non-peptide antagonist of substance P (SP), competitively inhibits the binding of [3H]SP to neurokinin receptor 1 (NK1 receptor) in rat brain membranes with a Ki value of 4.16 nM. RP 67580 is a specific antagonist of NK1 receptors and can be used in the research of pain and neurogenic inflammation[1]. |
| Name | (3aR,7aR)-2-[2-(2-methoxyphenyl)ethanimidoyl]-7,7-diphenyl-1,3,3a,5,6,7a-hexahydroisoindol-4-one |
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| Synonym | More Synonyms |
| Description | RP 67580 is a non-peptide antagonist of substance P (SP), competitively inhibits the binding of [3H]SP to neurokinin receptor 1 (NK1 receptor) in rat brain membranes with a Ki value of 4.16 nM. RP 67580 is a specific antagonist of NK1 receptors and can be used in the research of pain and neurogenic inflammation[1]. |
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| Related Catalog | |
| In Vivo | RP 67580（0.03-1 mg/kg；静脉注射；单剂量）显著抑制神经源性炎症。 Animal Model: Male albino Sprague-Dawley rats Dosage: 0.03, 0.1, 0.3, 1 mg/kg Administration: i.v.; single dose Result: Potently and dose-dependently inhibited the strong plasma extravasation caused by electrical stimulation of the saphenous nerve for 15 minutes with an ED50 value of 0.15 mg/kg. |
| References |
| Density | 1.17 g/cm3 |
|---|---|
| Boiling Point | 588.5ºC at 760 mmHg |
| Melting Point | 195-188ºC |
| Molecular Formula | C29H30N2O2 |
| Molecular Weight | 438.56 |
| Flash Point | 309.7ºC |
| Exact Mass | 438.23100 |
| PSA | 53.39000 |
| LogP | 5.14980 |
| Vapour Pressure | 7.89E-14mmHg at 25°C |
| Index of Refraction | 1.626 |
| Tocris-1635 |
| RP-67580 |