Taltirelin acetate
CAS No. 1549593-23-8
Taltirelin acetate( TA-0910 acetate )
Catalog No. M22365 CAS No. 1549593-23-8
Taltirelin acetate is a superagonist at thyrotropin-releasing hormone receptor (TRH-R)(IC50 of 910 nM and EC50 of 36 nM for stimulating an increase in cytosolic Ca2+ concentration (Ca2+ release)).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 49 | In Stock |
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| 2MG | 29 | In Stock |
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| 5MG | 45 | In Stock |
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| 10MG | 73 | In Stock |
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| 25MG | 144 | In Stock |
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| 50MG | 237 | In Stock |
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| 100MG | 369 | In Stock |
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| 200MG | 547 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameTaltirelin acetate
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NoteResearch use only, not for human use.
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Brief DescriptionTaltirelin acetate is a superagonist at thyrotropin-releasing hormone receptor (TRH-R)(IC50 of 910 nM and EC50 of 36 nM for stimulating an increase in cytosolic Ca2+ concentration (Ca2+ release)).
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DescriptionTaltirelin acetate is a superagonist at thyrotropin-releasing hormone receptor (TRH-R)(IC50 of 910 nM and EC50 of 36 nM for stimulating an increase in cytosolic Ca2+ concentration (Ca2+ release)).
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In Vitro——
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In Vivo——
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SynonymsTA-0910 acetate
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PathwayOthers
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TargetOther Targets
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RecptorTHR
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Research AreaNervous system
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IndicationSpinocerebellar Degeneration
Chemical Information
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CAS Number1549593-23-8
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Formula Weight465.46
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Molecular FormulaC19H27N7O7
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Purity>98% (HPLC)
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SolubilityDMSO:125 mg/mL (268.55 mM; Need ultrasonic)
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SMILESO=C(N(CCC1)[C@@H]1C(N)=O)[C@@H](NC([C@@H](NC2=O)CC(N2C)=O)=O)CC3=CN=CN3.CC(O)=O
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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
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A 1120
A 1120 is a nonretinoid retinol-binding protein 4 (RBP4) antagonist (Ki: 8.3 nM), which disrupts the interaction between RBP4 and its binding partner transthyretin.
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2',5'-Dideoxyadenosi...
2',5'-Dideoxyadenosine is a potent and non-competitive adenylyl cyclase inhibitor via binding the P-site (IC50: 3 μM).2',5'-Dideoxyadenosine (20-150 mM), like adenosine, dependently and reversibly inhibits the positive inotropic and chronotropic effect of beta-adrenergic stimulation with isoproterenol (8-54 pmol) up to 70% and 50%, respectively.
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Dimethyl DL-Glutamat...
Dimethyl DL-glutamate is a cell-permeant glutamic acid derivative that enhances insulin release in response to glucose in isolated islets and in animal models of diabetes.
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