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(3aR,7aR)-Octahydro-2-[1-imino-2-(2-methoxyphenyl)ethyl]-7,7-diphenyl-4H-isoindol-4-one manufacturers
- RP 67580
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2025-12-22
- CAS:135911-02-3
- Purity:
- Supply Ability: 10g
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| | (3aR,7aR)-Octahydro-2-[1-imino-2-(2-methoxyphenyl)ethyl]-7,7-diphenyl-4H-isoindol-4-one Basic information |
| Product Name: | (3aR,7aR)-Octahydro-2-[1-imino-2-(2-methoxyphenyl)ethyl]-7,7-diphenyl-4H-isoindol-4-one | | Synonyms: | RP 67580;(3aR,7aR)-Octahydro-2-(1-imino-2-(2-methoxyphenyl)ethyl)-7,7-diphenyl-4H-isoindol;4H-Isoindol-4-one, octahydro-2-(1-imino-2-(2-methoxyphenyl)ethyl)-7,7-diphenyl-, (3ar,7ar)-;4H-Isoindol-4-one, octahydro-2-(1-imino-2-(2-methoxyphenyl)ethyl)-7,7-diphenyl-, (3ar-cis)-;7,7-Diphenyl-2-(1-imino-2-(2-methoxyphenyl)ethyl)perhydroisoindol-4-one;Rp 68651;(3aR,7aR)-2-(1-Imino-2-(2-methoxyphenyl)ethyl)-7,7-diphenylhexahydro-1H-isoindol-4(2H)-one;(3aR,7aR)-Octahydro-2-[1-imino-2-(2-methoxyphenyl)ethyl]-7,7-diphenyl-4H-isoindol-4-one | | CAS: | 135911-02-3 | | MF: | C29H30N2O2 | | MW: | 438.56 | | EINECS: | | | Product Categories: | Tachykinin receptor | | Mol File: | 135911-02-3.mol | ![(3aR,7aR)-Octahydro-2-[1-imino-2-(2-methoxyphenyl)ethyl]-7,7-diphenyl-4H-isoindol-4-one Structure](CAS/GIF/135911-02-3.gif) |
| | (3aR,7aR)-Octahydro-2-[1-imino-2-(2-methoxyphenyl)ethyl]-7,7-diphenyl-4H-isoindol-4-one Chemical Properties |
| storage temp. | Store at +4°C | | solubility | Soluble to 100 mM in ethanol and to 50 mM in DMSO | | form | Powder |
| | (3aR,7aR)-Octahydro-2-[1-imino-2-(2-methoxyphenyl)ethyl]-7,7-diphenyl-4H-isoindol-4-one Usage And Synthesis |
| Uses | RP 67580 is a neurokinin-1 receptor (NK1) antagonist. | | Biological Activity | Potent and selective tachykinin NK 1 receptor antagonist (K i values are 2.9 nM and > 10 μ M for rat NK 1 , and rat NK 2 and NK 3 receptors respectively). Displays higher affinity at rat and mouse than human receptors. Antinociceptive in vivo , possibly partly via inhibition of calcium channels. | | in vivo | RP 67580 (0.03-1 mg/kg; i.v.; single dose) significantly inhibits neurogenic inflammation. | 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. |
| | storage | Store at -20°C |
| | (3aR,7aR)-Octahydro-2-[1-imino-2-(2-methoxyphenyl)ethyl]-7,7-diphenyl-4H-isoindol-4-one Preparation Products And Raw materials |
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