D-Leucine structure, CAS 328-38-1

D-Leucine

CAS Number328-38-1

Synonymsleucine; D-Leucine; MFCD00063088; (R)-2-Amino-4-methylpentanoic acid; (2R)-2-amino-4-methylpentanoic acid; ent-1; H-Leu-OH; D-Homo-valine; D-2-Amino-4-methylvaleric acid; H-D-Leu-OH; (R)-2-Amino-4-methyl-pentanoic acid; EINECS 206-327-7; D-2-Amino-4-methylpentanoicacid

Molecular Formula(CH3)2CHCH2CH(NH2)CO2H

Molecular Weight131.17

Purity99%

Density1.0±0.1 g/cm3

Boiling Point225.8±23.0 °C at 760 mmHg

Melting Point>300 °C (lit.)

Flash Point

Appearancepowder (crystals)

EINECS206-327-7

MSDSChineseEnglish

SymbolTransport

Signal WordWarning

Cat. No.: 2A-9007643 Purity: 99%
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Chemical & Physical Properties
CAS Number328-38-1
Catalog No.2A-9007643
Chinese NameD-亮氨酸
Synonymsleucine; D-Leucine; MFCD00063088; (R)-2-Amino-4-methylpentanoic acid; (2R)-2-amino-4-methylpentanoic acid; ent-1; H-Leu-OH; D-Homo-valine; D-2-Amino-4-methylvaleric acid; H-D-Leu-OH; (R)-2-Amino-4-methyl-pentanoic acid; EINECS 206-327-7; D-2-Amino-4-methylpentanoicacid
Molecular Formula(CH3)2CHCH2CH(NH2)CO2H
Molecular Weight131.17
Purity99
Density1.0±0.1 g/cm3
Boiling Point225.8±23.0 °C at 760 mmHg
Melting Point>300 °C (lit.)
Appearancepowder (crystals)
Storage ConditionShould be sealed and stored dry.
ApplicationD-Leucine has anti-epileptic activity and is more active than L-leucine. D-leucine effectively terminates epileptic seizures. In vitro, D-Leucine can reduce long-term site formation, but has no effect
EINECS206-327-7
HTC2922499990
PubChem ID24888380
MDL NumberMFCD00063088
SMILESCC(C)C[C@@H](N)C(O)=O
InChI1S/C6H13NO2/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t5-/m1/s1
InChI KeyROHFNLRQFUQHCH-RXMQYKEDSA-N
Beilstein/REAXYS1721721
NACRES CodeNA.22
UNSPSC12352209
Hazard SymbolsTransport
MSDSmsds/7643_2_328_38_1.pdf
BioactivityD-Leucine is a more potent anti-seizure agent than L-leucine. D-leucine potently terminates seizures even after the onset of seizure activity. D-leucine, but not L-leucine, reduces long-term potentiation but had no effect on basal synaptic transmission in vitro[1]. Related Catalog Research Areas >> Neurological Disease Target Human Endogenous Metabolite In Vitro In a screen of candidate neuronal receptors, D-leucine failed to compete for binding by cognate ligands, potentially suggesting a novel target. Even at low doses, D-leucine suppressed ongoing seizures at least as effectively as diazepam but without sedative effects. These studies raise the possibility that D-leucine may represent a new class of anti-seizure agents, and that D-leucine may have a previously unknown function in eukaryotes[1]. References [1]. Xiaoyu Cao, et al. Combination of PARP Inhibitor and Temozolomide to Suppress Chordoma Progression. J Mol Med (Berl). 2019 Aug;97(8):1183-1193 Chemical & Physical Properties Density 1.0±0.1 g/cm3 Boiling Point 225.8±23.0 °C at 760 mmHg Melting Point > 300ºC Molecular Formula C6H13NO2 Molecular Weight 131.173 Flash Point 90.3±22.6 °C Exact Mass 131.094635 PSA 63.32000 LogP 0.73 Vapour Pressure 0.0±0.9 mmHg at 25°C Index of Refraction 1.463 InChIKey ROHFNLRQFUQHCH-RXMQYKEDSA-N SMILES CC(C)CC(N)C(=O)O
Use ofD-Leucine is a more potent anti-seizure agent than L-leucine. D-leucine potently terminates seizures even after the onset of seizure activity. D-leucine, but not L-leucine, reduces long-term potentiation but had no effect on basal synaptic transmission in vitro[1]. Properties Name D-leucine Synonym More Synonyms H-D-Leu-OH Biological Activity Description D-Leucine is a more potent anti-seizure agent than L-leucine. D-leucine potently terminates seizures even after the onset of seizure activity. D-leucine, but not L-leucine, reduces long-term potentiation but had no effect on basal synaptic transmission in vitro[1]. Related Catalog Research Areas >> Neurological Disease Human Endogenous Metabolite In Vitro In a screen of candidate neuronal receptors, D-leucine failed to compete for binding by cognate ligands, potentially suggesting a novel target. Even at low doses, D-leucine suppressed ongoing seizures at least as effectively as diazepam but without sedative effects. These studies raise the possibility that D-leucine may represent a new class of anti-seizure agents, and that D-leucine may have a previously unknown function in eukaryotes[1]. References [1]. Xiaoyu Cao, et al. Combination of PARP Inhibitor and Temozolomide to Suppress Chordoma Progression. J Mol Med (Berl). 2019 Aug;97(8):1183-1193 Chemical & Physical Properties Molecular Formula C6H13NO2 Exact Mass 131.094635 PSA 63.32000 Index of Refraction 1.463 InChIKey ROHFNLRQFUQHCH-RXMQYKEDSA-N SMILES CC(C)CC(N)C(=O)O
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Transport InfoProduct name: Purity: 98.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available
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