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ChemicalBook--->CAS DataBase List--->210580-75-9

210580-75-9

210580-75-9 Structure

210580-75-9 Structure
IdentificationBack Directory
[Name]

1-((S)-2-AMINO-PROPYL)-1H-INDAZOL-6-OL
[CAS]

210580-75-9
[Synonyms]

AL 34497
AL-34662
1-((S)-2-AMINO-PROPYL)-1H-INDAZOL-6-OL
1H-Indazol-6-ol, 1-[(2S)-2-aminopropyl]-
[Molecular Formula]

C10H13N3O
[MDL Number]

MFCD09031487
[MOL File]

210580-75-9.mol
[Molecular Weight]

191.23
Chemical PropertiesBack Directory
[Melting point ]

170-172 °C(Solv: dichloromethane (75-09-2))
[Boiling point ]

372.8±22.0 °C(Predicted)
[density ]

1.31±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

≤1mg/ml in ethanol;10mg/ml in DMSO;10mg/ml in dimethyl formamide
[form ]

crystalline solid
[pka]

9.30±0.40(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

AL-34662 is a selective 5-HT2A receptoragonist (IC50: 0.77 nM and 1.5 nM for rat and human 5-HT2 receptor). AL-34662 is also a weak α-1D adrenergic agonist activity (EC50:0.4 μM). AL-34662 is an ocular hypotensive agent[1][2].
[Biological Activity]

al 34662 is a potent 5-ht2 receptor agonist.serotonin (5-hydroxytryptamine; 5-ht) is a major neurotransmitter in the central nervous system (cns) of mammals and has welldocumented physiological functions in numerous cells, tissues, and organs.
[in vitro]

al-34662 exhibited a high affinity for the rat and human 5-ht2 receptor and for cloned human 5-ht2a-c receptors. al-34662 stimulated phosphoinositide turnover in human ciliary muscle and in human trabecular meshwork cells. al-34662 also mobilized intracellular ca2+ in h-cm and h-tm cells, being a full agonist like 5-ht itself. al-34662's effects in the h-cm cells were potently antagonized by 5-ht2a-antagonist m-100907, but weakly by 5-ht2b-antagonist, 5-ht2b/c- antagonist and 5-ht2c antagonist. moreover, it was found that the (r)-enantiomer (al-34707) and the racemate (al-34497) were less potent and/or efficacious than al-34662 in all of these assays [1].
[in vivo]

al-34662 caused relatively minimal ocular discomfort and hyperemia in rabbit and guinea pig eyes. it efficaciously lowered intraocular pressure in the conscious ocular hypertensive monkey eyes [1].
[IC 50]

0.8-1.5 nm for rat and human 5-ht2 receptor
[storage]

Store at -20°C
[References]

[1] sharif na, mclaughlin ma, kelly cr. al-34662: a potent, selective, and efficacious ocular hypotensive serotonin-2 receptor agonist. j ocul pharmacol ther. 2007 feb;23(1):1-13.
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