Dihydroergotamine-d3
Dihydroergotamine-d3 is the d3-labeled Dihydroergotamine (HY-B0670). Dihydroergotamine (DFN-19) is a blood-brain barrier-permeable semi-synthetic ergot alkaloid, acting as a full agonist of 5-HT1B/1D receptors (Ki values of 0.3 nM and 2.5 nM, respectively; functional IC50 values of 2 nM and 2.2 nM, respectively). Dihydroergotamine inhibits Forskolin (HY-15371)-stimulated cAMP accumulation, possesses α-adrenergic receptor antagonistic activity and weak dopaminergic agonistic activity. It mediates intracranial cerebrovascular contraction, inhibits the release of neuropeptides such as CGRP/substance P, and suppresses neurogenic inflammation by activating 5-HT1B/1D receptors in the trigeminovascular system. Dihydroergotamine binds to the catalytic site of Trypanosoma cruzi trypanothione reductase and exhibits trypanocidal activity in vitro. Dihydroergotamine can be used in studies related to migraine and trypanosome infections.
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- 화학식: C33H34D3N5O5
- 분자량:586.70
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Adrenergic Receptor Isoforms
MoreAll 5-HT Receptor Isoforms
MoreAll Dopamine Receptor Isoforms
MoreAll Parasite Isoforms
More
Biological Activity
제품 설명
IC50 & Target
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α adrenergic receptor |
human 5-HT1B Receptor 0.3 nM (Ki) |
human 5-HT1D Receptor 2.5 nM (Ki) |
신청
1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Chemical Information
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Unlabeled CAS 511-12-6
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분자량 586.70
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화학식 C33H34D3N5O5
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SMILES
O=C([C@H](C[C@]12[H])CN(C([2H])([2H])[2H])[C@]2([H])CC3=CNC4=C3C1=CC=C4)N[C@@](O5)(C)C(N6[C@]5(O)[C@@](CCC7)([H])N7C([C@@H]6CC8=CC=CC=C8)=O)=O
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)