H-Leu-Gly-OH
H-Leu-Gly-OH structure
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Common Name | H-Leu-Gly-OH | ||
|---|---|---|---|---|
| CAS Number | 686-50-0 | Molecular Weight | 188.22400 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C8H16N2O3 | Melting Point | -245ºC (dec.) | |
| MSDS | Chinese USA | Flash Point | N/A | |
Use of H-Leu-Gly-OHH-Leu-Gly-OH is a Glycine (HY-Y0966) derivative[1]. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | Leu-Gly |
|---|---|
| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | H-Leu-Gly-OH is a Glycine (HY-Y0966) derivative[1]. |
|---|---|
| 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 |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Melting Point | -245ºC (dec.) |
|---|---|
| Molecular Formula | C8H16N2O3 |
| Molecular Weight | 188.22400 |
| Exact Mass | 188.11600 |
| PSA | 92.42000 |
| LogP | 0.65180 |
| Index of Refraction | 86 ° (C=2, H2O) |
| InChIKey | LESXFEZIFXFIQR-LURJTMIESA-N |
| SMILES | CC(C)CC(N)C(=O)NCC(=O)O |
| Storage condition | −20°C |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Hazard Codes | Xi |
|---|---|
| Safety Phrases | S22-S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2924199090 |
This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 8 | |
|---|---|
| DownStream 1 | |
CAS#:26117-20-4
CAS#:6000-44-8
CAS#:56-40-6
CAS#:3190-70-3
CAS#:2706-38-9
CAS#:72-18-4![2-[(2-bromo-4-methyl-pentanoyl)amino]acetic acid Structure](https://image.chemsrc.com/caspic/320/7154-27-0.png)
CAS#:7154-27-0
CAS#:1738-89-2This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.
| HS Code | 2924199090 |
|---|---|
| Summary | 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
This table lists relevant public references with title, journal and publication metadata for this compound.
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Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.
Nat. Chem. Biol. 5 , 45-52, (2009) Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr... |
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Copper(II)- cis, cis-1,3,5-triaminocyclohexane complex-promoted hydrolysis of dipeptides: kinetic, speciation and structural studies.
J. Biol. Inorg. Chem. 7 , 843-851, (2002) The hydrolysis of glycylglycine (GylGly), glycyl-L-leucine (GlyLeu), L-leucylglycine (LeuGly) and glycyl-DL-serine (GlySer) promoted by a copper(II)- cis, cis-1,3,5-triaminocyclohexane complex [Cu(II)... |
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Cleavage of L-leucine-containing dipeptides by Clostridium butyricum. Khelifa N, Brik M, Tessedre AC, et al.
Bioorg. Med. Chem. 9 , 109-112, (1999)
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This table contains target information, in‑vitro & in‑vivo assay data for this compound.
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Name: Bitter tasting threshold was expressed as log 1/T.
Source: ChEMBL
Target: N/A
External Id: CHEMBL847173
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Name: Induction of nitrogen-starved wild type sigma1278b yeast Gap1-mediated amino acid upt...
Source: ChEMBL
Target: General amino-acid permease GAP1
External Id: CHEMBL1228077
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Name: Induction of nitrogen-starved wild type sigma1278b yeast Gap1-mediated trehalose acti...
Source: ChEMBL
Target: General amino-acid permease GAP1
External Id: CHEMBL1228076
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Name: Competitive inhibition of nitrogen-starved wild type sigma1278b yeast Gap1-mediated a...
Source: ChEMBL
Target: General amino-acid permease GAP1
External Id: CHEMBL1228072
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Name: Induction of nitrogen-starved wild type sigma1278b yeast Gap1-mediated trehalose acti...
Source: ChEMBL
Target: General amino-acid permease GAP1
External Id: CHEMBL1228306
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Name: Biological activity was measured against Angiotensin I converting enzyme
Source: ChEMBL
Target: Angiotensin-converting enzyme
External Id: CHEMBL858254
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This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| (S)-2-(2-Amino-4-methylpentanamido)acetic acid |
| 2-[[(2S)-2-amino-4-methylpentanoyl]amino]acetic acid,hydrate |
| MFCD00065940 |
| EINECS 211-688-9 |
| H-Leu-Gly-OH |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What is the melting point of Leu-Gly? |
| A: Melting point of Leu-Gly is -245ºC (dec.). |
| Q: What are the downstream products of Leu-Gly? |
| A: Related downstream products(CAS) of Leu-Gly: 2706-38-9. |
| Q: What are the storage conditions for Leu-Gly? |
| A: Storage conditions for Leu-Gly: −20°C. |
| Q: What English synonyms does Leu-Gly have? |
| A: English synonyms of Leu-Gly: (S)-2-(2-Amino-4-methylpentanamido)acetic acid, 2-[[(2S)-2-amino-4-methylpentanoyl]amino]acetic acid,hydrate, MFCD00065940, EINECS 211-688-9, H-Leu-Gly-OH. |
| Q: What are the upstream materials of Leu-Gly? |
| A: Related upstream materials(CAS) of Leu-Gly: 26117-20-4;6000-44-8;56-40-6;3190-70-3;2706-38-9;72-18-4;7154-27-0;1738-89-2. |
| Q: What is the CAS number of Leu-Gly? |
| A: CAS number of Leu-Gly is 686-50-0. |
| Q: What is the SMILES notation of Leu-Gly? |
| A: SMILES notation of Leu-Gly is CC(C)CC(N)C(=O)NCC(=O)O. |
| Q: What are the uses of Leu-Gly? |
| A: Main uses of Leu-Gly: H-Leu-Gly-OH is a Glycine (HY-Y0966) derivative[1]. |
| Q: What is the LogP of Leu-Gly? |
| A: LogP of Leu-Gly is 0.65180. |
| Q: What is the molecular weight of Leu-Gly? |
| A: Molecular weight of Leu-Gly is 188.22400. |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |
| Dayang Chem (Hangzhou) Co., Ltd. |