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D-(-)-Tartaric acid
CAS No. 147-71-7
D-(-)-Tartaric acid( D-Tartaric acid )
Catalog No. M19565 CAS No. 147-71-7
D-Tartaric acid also known as (SS)-tartarate or D-threaric acid belongs to the class of organic compounds known as sugar acids and derivatives.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 37 | In Stock |
|
| 5MG | 48 | In Stock |
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| 10MG | 68 | In Stock |
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| 25MG | 41 | In Stock |
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| 50MG | 59 | In Stock |
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| 100MG | 85 | In Stock |
|
| 200MG | 124 | In Stock |
|
| 500MG | 210 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameD-(-)-Tartaric acid
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NoteResearch use only, not for human use.
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Brief DescriptionD-Tartaric acid also known as (SS)-tartarate or D-threaric acid belongs to the class of organic compounds known as sugar acids and derivatives.
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DescriptionD-Tartaric acid also known as (SS)-tartarate or D-threaric acid belongs to the class of organic compounds known as sugar acids and derivatives. Within the cell D-tartaric acid is primarily located in the cytoplasm. D-Tartaric acid can be converted into (2S3S)-cis-fertaric acid and (2S3S)-trans-fertaric acid. Outside of the human body D-tartaric acid can be found in vinegar. This makes D-tartaric acid a potential biomarker for the consumption of this food product.
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In Vitro——
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In Vivo——
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SynonymsD-Tartaric acid
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number147-71-7
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Formula Weight150.09
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Molecular FormulaC4H6O6
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESO[C@@H]([C@H](O)C(O)=O)C(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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Succimer
Succimer is a Lead Chelator. The mechanism of action of succimer is as a Lead Chelating Activity.
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Ac-YVAD-pNA
Ac-YVAD-pNA is a specific Caspase-1 substrate. Ac-YVAD-pNA can be used to detect Caspase-1 activity. Caspase-1 is a key mediator of inflammatory processes.
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Compound K
HIV-IN-11 is part of the hydroxylaminoglutaramide (HAPA) transition state isomeric series of HIV protease inhibitors and is a potent and selective inhibitor of HIV-1 protease. HIV-IN-11 competitively inhibits HIV-1 PR (Ki: 0.049 nM) and potently inhibits replication of HIV(IIIb)-infected MT4 lymphocytes at concentrations of 25.0-50.0 nM. HIV-IN-11 displays a longer half-life than indinavir sulfate in animal models and serves as a promising second-generation HIV protease inhibitor.
