Name | 2,2'-[(6R,11R,12E,14S,15E,16aS,23E,25S,26E,27aS)-6-({(2S,5S,8S,11S)-2-(4-Aminobutyl)-1,4,7,10,13-pentahydroxy-8-(2-hydroxy-2-iminoethyl)-5,11-bis(hydroxymethyl)-13-[(2S)-1-(L-seryl)-2-pyrrolidinyl]-3,6,9,12-tetraazatrideca-3,6,9,12-tetraen-1-ylidene}amino)-11-{(3S,6S,12S,15S)-3-benzyl-1,4,7,10,13-pentahydroxy-15-[hydroxy(imino)methyl]-12-isobutyl-6-isopropyl-18-thia-2,5,8,11,14-pentaazanonadeca-1,4,7,10,13-pentaen-1-yl}-13,16,24,27-tetrahydroxy-5,21-dioxo-2,3,6,7,11,14,16a,17,18,19,21,22,25,27a-tetradecahydro-1H,5H,10H-dipyrrolo[2,1-j:2',1'-s][1,2,5,8,11,14,17,20]dithiahexaazacyclotricosine-14,25-diyl]diacetic acid |
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Synonyms | Scyliorhinin II |
Description | Scyliorhinin II is a selective neurokinin-3 receptor agonist, with a Ki of 2.5 nM for neurokinin-3 receptor in rat cerebral cortex. |
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Related Catalog | |
Target |
Ki: 2.5 nM (Neurokinin-3 receptor)[1] |
In Vitro | Scyliorhinin II is a neurokinin-3 selective tachykinin receptor, with a Ki of 2.5 nM for neurokinin-3 (NK-3) receptor in rat cerebral cortex. Scyliorhinin II has little effect on NK-1 and NK-2 receptors, with Ki (NK-1 receptor)/Ki (NK-3 receptor) and Ki (NK-2 receptor)/Ki (NK-3 receptor) of 176 and 200[1]. |
In Vivo | Scyliorhinin II produces potent, dose-related reciprocal hindlimb scratching about equipotently with an ED50 of 0.08 nmol via intracerebroventricularly (i.c.v.) administration in mice[2]. |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 1817.4±75.0 °C at 760 mmHg |
Molecular Formula | C77H119N21O26S3 |
Molecular Weight | 1851.089 |
Flash Point | 1052.9±37.1 °C |
Exact Mass | 1849.779663 |
LogP | 0.42 |
Vapour Pressure | 0.0±0.3 mmHg at 25°C |
Index of Refraction | 1.696 |
Storage condition | 2-8℃ |