| Bioactivity | Olanzapine-d3 is the deuterium labeled Olanzapine. Olanzapine is a selective, orally active monoaminergic antagonist with high affinity binding to serotonin H1, 5HT2A/2C, 5HT3, 5HT6 (Ki=7, 4, 11, 57, and 5 nM, respectively), dopamine D1-4 (Ki=11 to 31 nM), muscarinic M1-5 (Ki=1.9-25 nM), and adrenergic α1 receptors (Ki=19 nM). Olanzapine is an atypical antipsychotic[1][2]. | ||||||||||||
| Name | Olanzapine-d3 | ||||||||||||
| CAS | 786686-79-1 | ||||||||||||
| Formula | C17H17D3N4S | ||||||||||||
| Molar Mass | 315.45 | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
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Olanzapine-d3
CAS: 786686-79-1 F: C17H17D3N4S W: 315.45
Olanzapine-d3 is the deuterium labeled Olanzapine. Olanzapine is a selective, orally active monoaminergic antagonist wit
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