L-3-Pyrroline-2-carboxylic acid structure
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Common Name | L-3-Pyrroline-2-carboxylic acid | ||
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CAS Number | 3395-35-5 | Molecular Weight | 113.115 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 279.3±40.0 °C at 760 mmHg | |
Molecular Formula | C5H7NO2 | Melting Point | 245ºC (dec.)(lit.) | |
MSDS | Chinese USA | Flash Point | 122.7±27.3 °C |
Use of L-3-Pyrroline-2-carboxylic acid3,4-Dehydro-DL-proline is a proline derivative[1]. |
Name | 3,4-dehydro-dl-proline |
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Synonym | More Synonyms |
Description | 3,4-Dehydro-DL-proline is a proline derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 279.3±40.0 °C at 760 mmHg |
Melting Point | 245ºC (dec.)(lit.) |
Molecular Formula | C5H7NO2 |
Molecular Weight | 113.115 |
Flash Point | 122.7±27.3 °C |
Exact Mass | 113.047676 |
PSA | 49.33000 |
LogP | 0.10 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.521 |
Storage condition | -15°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Risk Phrases | R22 |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933990090 |
~76% L-3-Pyrroline-2... CAS#:3395-35-5 |
Literature: Synthetic Communications, , vol. 10, # 7 p. 529 - 540 |
Precursor 1 | |
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DownStream 0 |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Many amino acid substitutions in a hypoxia-inducible transcription factor (HIF)-1alpha-like peptide cause only minor changes in its hydroxylation by the HIF prolyl 4-hydroxylases: substitution of 3,4-dehydroproline or azetidine-2-carboxylic acid for the proline leads to a high rate of uncoupled 2-oxoglutarate decarboxylation.
J. Biol. Chem. 279(53) , 55051-9, (2004) Three human prolyl 4-hydroxylases (P4Hs) regulate the hypoxia-inducible transcription factors (HIFs) by hydroxylating a Leu-Xaa-Xaa-Leu-Ala-Pro motif. We report here that the two leucines in the Leu-G... |
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Overexpression of decorin by rat arterial smooth muscle cells enhances contraction of type I collagen in vitro.
Arterioscler. Thromb. Vasc. Biol. 24(1) , 67-72, (2004) Overexpression of decorin reduces neointimal thickening in balloon-injured carotid arteries of rats by decreasing the volume of neointimal extracellular matrix (ECM). We examined the hypothesis that d... |
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Enhanced and feedback-resistant gamma-glutamyl kinase activity of an Escherichia coli transformant carrying a mutated proB gene of Streptococcus thermophilus.
FEMS Microbiol. Lett. 182(1) , 143-7, (2000) We used a PCR-based method to generate a single base pair mutation in the proB gene of Streptococcus thermophilus, which replaced an aspartic acid with a glycine residue at position 192 of the first p... |
3,4-Dehydro-DL-proline |
3,4-dehydro-D,L-proline |
H-DL-PRO(3,4-DEHYDRO)-OH |
3,4-DIDEHYDRO-DL-PROLINE |
L-3-Pyrroline-2-carboxylic acid |
rac-(2R*)-3-Pyrroline-2-carboxylic acid |
EINECS 222-243-3 |
R,S-3,4-dehydroproline |
2,5-Dihydro-1H-pyrrole-2-carboxylic acid |
H-DL-DELTAPRO-OH |
H-3,4-DEHYDRO-DL-PRO-OH |
D,L-3,4-dehydroproline |
1H-Pyrrole-2-carboxylic acid, 2,5-dihydro- |
3,4-Dedihydro-DL-proline |
3,4-Dehydro-DL-prolin |
(+/-)-3-PYRROLINE-2-CARBOXYLIC ACID |
2,5-dihydro-pyrrole-2-carboxylic acid |
3,4-Dedihydroproline |
MFCD00005214 |