(S)-3-Hydroxyphenylglycine
CAS No. 71301-82-1
(S)-3-Hydroxyphenylglycine( —— )
Catalog No. M27701 CAS No. 71301-82-1
(S)-3-Hydroxyphenylglycine is an agonist of group I metabotropic glutamate receptors (mGluRs).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 105 | In Stock |
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| 10MG | 150 | In Stock |
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| 25MG | 250 | In Stock |
|
| 50MG | 351 | In Stock |
|
| 100MG | 481 | In Stock |
|
| 200MG | 646 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product Name(S)-3-Hydroxyphenylglycine
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NoteResearch use only, not for human use.
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Brief Description(S)-3-Hydroxyphenylglycine is an agonist of group I metabotropic glutamate receptors (mGluRs).
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Description(S)-3-Hydroxyphenylglycine is an agonist of group I metabotropic glutamate receptors (mGluRs).(In Vitro):Hippocampal neurons in the slice preparation exhibit spontaneous synchronized bursting activity in the presence of picrotoxin, a γ-aminobutyric acid-A receptor antagonist. These synchronized bursts rarely exceed 500 ms in duration and thus resemble interictal discharges. Control shows one such synchronized burst, which typically consisted of an initial abrupt discharge 100–200 ms in duration (primary burst) followed by a series of briefer phasic discharges (secondary bursts). Addition of (S)-3-hydroxyphenylglycine (250–500 μM) significantly prolonged the synchronized burst duration, primarily via a marked increase in the number of secondary bursts. These prolonged discharges ranged from 1 to 7 s in duration (4,282 ± 1,060 ms, a 1,021 ± 247% increase, n = 7), and the secondary bursts within each discharge gradually changed in amplitude and frequency.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayNeuroscience
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TargetGluR
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RecptorJAK
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Research Area——
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Indication——
Chemical Information
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CAS Number71301-82-1
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Formula Weight167.16
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Molecular FormulaC8H9NO3
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Purity>98% (HPLC)
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Solubility——
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SMILESN[C@@](C(O)=O)([H])C1=CC(O)=CC=C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Paul R. Fatheree, et al. JAK Kinase Inhibitor Compounds for Treatment of Respiratory Disease. US20170121327A1
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