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10329-75-6,MFCD00038309
Catalog No.:AA00H9Y5

10329-75-6 | H-Leu-leu-leu-oh

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
≥ 96% (Elemental Analysis)
in stock  
$152.00   $107.00
- +
1g
≥ 96% (Elemental Analysis)
in stock  
$269.00   $189.00
- +
5g
≥ 96% (Elemental Analysis)
in stock  
$922.00   $645.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00H9Y5
Chemical Name:
H-Leu-leu-leu-oh
CAS Number:
10329-75-6
Molecular Formula:
C18H35N3O4
Molecular Weight:
357.4882
MDL Number:
MFCD00038309
SMILES:
CC(C[C@@H](C(=O)N[C@H](C(=O)O)CC(C)C)NC(=O)[C@H](CC(C)C)N)C
Properties
Computed Properties
 
Complexity:
450  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
3  
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
4  
Rotatable Bond Count:
11  
XLogP3:
-0.9  

Downstream Synthesis Route

[1]Albrecht;Spiess;Schneider[Synthesis,2002,#1,p.126-132]

[1]Albrecht;Spiess;Schneider[Synthesis,2002,#1,p.126-132]

10329-75-6   
N-((S)-1-{(S)-1-(S)-1-(2,3-Dihydroxy-benzylcarbamoyl)-3-methyl-butylcarbamoyl-3-methyl-butylcarbamoyl}-3-methyl-butyl)-2,3-dihydroxy-benzamide 

[1]Albrecht;Spiess;Schneider[Synthesis,2002,#1,p.126-132]

61-90-5    3303-31-9    57791-42-1    62526-43-6    10329-75-6    18867-82-8   
penta(leucine) 
 
2-(2-{2-2-(2-{2-2-(2-amino-4-methyl-pentanoylamino)-4-methyl-pentanoylamino-4-methyl-pentanoylamino}-4-methyl-pentanoylamino)-4-methyl-pentanoylamino-4-methyl-pentanoylamino}-4-methyl-pentanoylamino)-4-methyl-pentanoicacid 
 
C54H101N9O10 

[1]Phosphorus,SulfurandSiliconandtheRelatedElements,2008,vol.183,p.691-698

[1]Bioscience,BiotechnologyandBiochemistry,2010,vol.74,p.129-134

Literature

Title: Two inhibitors of the ubiquitin proteasome system enhance long-term memory formation upon olfactory conditioning in the honeybee (Apis mellifera).

Journal: The Journal of experimental biology 20141001

Title: Distinct mechanisms of membrane permeation induced by two polymalic acid copolymers.

Journal: Biomaterials 20130101

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology 20090101

Title: A selective fluorescence reaction for peptides and chromatographic analysis.

Journal: Peptides 20080301

Title: Trileucine improves aerosol performance and stability of spray-dried powders for inhalation.

Journal: Journal of pharmaceutical sciences 20080101

Title: Trypanocidal activities of trileucine methyl vinyl sulfone proteasome inhibitors.

Journal: Parasitology research 20050101

Title: Identification of distinct roles for a dileucine and a tyrosine internalization motif in the interleukin (IL)-13 binding component IL-13 receptor alpha 2 chain.

Journal: The Journal of biological chemistry 20010706

Title: Importance of NF-kappaB in rheumatoid synovial tissues: in situ NF-kappaB expression and in vitro study using cultured synovial cells.

Journal: Annals of the rheumatic diseases 20010701

Quotation Request
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SDS
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Tags:10329-75-6 Molecular Formula|10329-75-6 MDL|10329-75-6 SMILES|10329-75-6 H-Leu-leu-leu-oh
Catalog No.: AA00H9Y5
10329-75-6,MFCD00038309
10329-75-6 | H-Leu-leu-leu-oh
Pack Size： 250mg
Purity： ≥ 96% (Elemental Analysis)
in stock
$152.00 $107.00
Pack Size： 1g
Purity： ≥ 96% (Elemental Analysis)
in stock
$269.00 $189.00
Pack Size： 5g
Purity： ≥ 96% (Elemental Analysis)
in stock
$922.00 $645.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00H9Y5
Chemical Name: H-Leu-leu-leu-oh
CAS Number: 10329-75-6
Molecular Formula: C18H35N3O4
Molecular Weight: 357.4882
MDL Number: MFCD00038309
SMILES: CC(C[C@@H](C(=O)N[C@H](C(=O)O)CC(C)C)NC(=O)[C@H](CC(C)C)N)C
Properties
Complexity: 450  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 3  
Heavy Atom Count: 25  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 4  
Rotatable Bond Count: 11  
XLogP3: -0.9  
Downstream Synthesis Route
1521-38-6    10329-75-6    408349-31-5 

[1]Albrecht;Spiess;Schneider[Synthesis,2002,#1,p.126-132]

10329-75-6    408349-54-2 

[1]Albrecht;Spiess;Schneider[Synthesis,2002,#1,p.126-132]

10329-75-6   
N-((S)-1-{(S)-1-(S)-1-(2,3-Dihydroxy-benzylcarbamoyl)-3-methyl-butylcarbamoyl-3-methyl-butylcarbamoyl}-3-methyl-butyl)-2,3-dihydroxy-benzamide 

[1]Albrecht;Spiess;Schneider[Synthesis,2002,#1,p.126-132]

61-90-5    3303-31-9    57791-42-1    62526-43-6    10329-75-6    18867-82-8   
penta(leucine) 
 
2-(2-{2-2-(2-{2-2-(2-amino-4-methyl-pentanoylamino)-4-methyl-pentanoylamino-4-methyl-pentanoylamino}-4-methyl-pentanoylamino)-4-methyl-pentanoylamino-4-methyl-pentanoylamino}-4-methyl-pentanoylamino)-4-methyl-pentanoicacid 
 
C54H101N9O10 

[1]Phosphorus,SulfurandSiliconandtheRelatedElements,2008,vol.183,p.691-698

72-18-4    61-90-5    3918-94-3    3303-31-9    28130-13-4    10329-75-6 

[1]Bioscience,BiotechnologyandBiochemistry,2010,vol.74,p.129-134

Literature fold

Title: Two inhibitors of the ubiquitin proteasome system enhance long-term memory formation upon olfactory conditioning in the honeybee (Apis mellifera).

Journal: The Journal of experimental biology20141001

Title: Distinct mechanisms of membrane permeation induced by two polymalic acid copolymers.

Journal: Biomaterials20130101

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology20090101

Title: A selective fluorescence reaction for peptides and chromatographic analysis.

Journal: Peptides20080301

Title: Trileucine improves aerosol performance and stability of spray-dried powders for inhalation.

Journal: Journal of pharmaceutical sciences20080101

Title: Trypanocidal activities of trileucine methyl vinyl sulfone proteasome inhibitors.

Journal: Parasitology research20050101

Title: Identification of distinct roles for a dileucine and a tyrosine internalization motif in the interleukin (IL)-13 binding component IL-13 receptor alpha 2 chain.

Journal: The Journal of biological chemistry20010706

Title: Importance of NF-kappaB in rheumatoid synovial tissues: in situ NF-kappaB expression and in vitro study using cultured synovial cells.

Journal: Annals of the rheumatic diseases20010701

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