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D-(-)-Lactic acid
CAS No. 10326-41-7
D-(-)-Lactic acid( (R)-2-Hydroxypropionic acid )
Catalog No. M23238 CAS No. 10326-41-7
D-(-)-Lactic acid is a normal intermediate in sugar fermentation (oxidation, metabolism).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 48 | In Stock |
|
| 5MG | 48 | In Stock |
|
| 100MG | 62 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 68 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameD-(-)-Lactic acid
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NoteResearch use only, not for human use.
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Brief DescriptionD-(-)-Lactic acid is a normal intermediate in sugar fermentation (oxidation, metabolism).
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DescriptionD-(-)-Lactic acid is a normal intermediate in sugar fermentation (oxidation, metabolism). It is identified as a competitive inhibitor of ProDH (proline dehydrogenase) in plants.
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In Vitro——
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In Vivo——
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Synonyms(R)-2-Hydroxypropionic acid
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PathwayProteasome/Ubiquitin
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TargetEndogenous Metabolite
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RecptorHuman Endogenous Metabolite|ProDH
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Research Area——
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Indication——
Chemical Information
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CAS Number10326-41-7
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Formula Weight90.08
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Molecular FormulaC3H6O3
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Purity>98% (HPLC)
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SolubilityDMSO: 125 mg/mL (1387.66 mM)
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SMILESC[C@@H](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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3-(2-Hydroxyphenyl)p...
3-(2-Hydroxyphenyl)propanoic acid also known as melilotic acid or melilotate. Within the cell 3-(2-hydroxyphenyl)propanoic acid is primarily located in the cytoplasm. 3-(2-Hydroxyphenyl)propanoic acid can be biosynthesized from propionic acid.
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L-Homocystine
Homocystine is the double-bonded form of homocysteine but it occurs only transiently before being converted to the harmless cystathionine via a vitamin B6-dependent enzyme. Increasing evidence supports a role for an elevation of homocysteine in schizophrenia.
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Phenylacetic acid
Phenyl acetate (or phenylacetate) is a carboxylic acid ester that has been found in the biofluids of patients with nephritis and/or hepatitis as well as patients with phenylketonuria (PKU) an inborn error of metabolism. Excess phenylalanine in the body can be disposed of through a transamination process leading to the production of phenylpyruvate.
