L-Isoleucine - Moligand™, 10mM in Water , CAS No.73-32-5

CAS: 73-32-5 Cat. No.: L425728 Summenformel: C₆H₁₃NO₂ Molekulargewicht: 131.18 Beilstein Registry Number: 4454 EG-Nummer: 200-798-2

QUALITÄT & REINHEIT Moligand™, 10mM in Water

Synonyms

l-isoleucine|Isoleucine|73-32-5|(2S,3S)-2-Amino-3-methylpentanoic acid|2S,3S-Isoleucine|(S)-Isoleucine|H-Ile-OH|(S,S)-Isoleucine|2-Amino-3-methylvaleric acid|L-(+)-Isoleucine|erythro-L-Isoleucine|L-Ile|ISOLEUCINE, L-|alpha-Amino-beta-methylvaleric acid|Is

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

L-Isoleucine is an essential amino acid used as a supplement in sports nutrition.[1] It is one of the free-amino acids found in common buckwheat.

Spezifikationen

Synonyme

l-isoleucine | Isoleucine | 73-32-5 | (2S,3S)-2-Amino-3-methylpentanoic acid | 2S,3S-Isoleucine | (S)-Isoleucine | H-Ile-OH | (S,S)-Isoleucine | 2-Amino-3-methylvaleric acid | L-(+)-Isoleucine | erythro-L-Isoleucine | L-Ile | ISOLEUCINE, L- | alpha-Amino-beta-methylvaleric acid | Is

Spezifikationen & Reinheit

Moligand™, 10mM in Water

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Note

Moligand™

Namen und Kennungen

Pubchem Sid

528765176

Kanonisches Lächeln

CC[C@H](C)[C@@H](C(=O)O)N

IUPAC Name

(2S,3S)-2-amino-3-methylpentanoic acid

InChIKey

AGPKZVBTJJNPAG-WHFBIAKZSA-N

INCHI

1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t4-,5-/m0/s1

Isomere SMILES

CC[C@H](C)[C@@H](C(=O)O)N

RTECS

NR4705000

Molekulargewicht

131.18

Beilstein

4454

Reaxy-Rn

1721790

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721790&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Ebene5 Amino acids and derivatives
          • Ebene6 Alpha amino acids and derivatives
            • Ebene7 Isoleucine and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Isoleucine and derivatives
• Alternative Parents: L-alpha-amino acids Methyl-branched fatty acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Isoleucine or derivatives - Alpha-amino acid - L-alpha-amino acid - Branched fatty acid - Methyl-branched fatty acid - Fatty acid - Fatty acyl - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxide - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as isoleucine and derivatives. These are compounds containing isoleucine or a derivative thereof resulting from reaction of isoleucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
• External Descriptors: Amino fatty acids

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Zugehörige Ziele (menschlich)

SLC7A5 Tchem L-type amino acid transporter 1 (388 Activities)

Discover Target: SLC7A5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC36A1 Tchem Proton-coupled amino acid transporter 1 (102 Activities)

Discover Target: SLC36A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Zugehörige Ziele (nicht menschlich)

Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)

Discover Target: Pkm

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slc16a10 Monocarboxylate transporter 10 (73 Activities)

Discover Target: Slc16a10

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Spezifische Drehung [α]: 40.5 ° (C=4, 6mol/L HCl)
• Schmelzpunkt (°C): 288 °C
• Molekulargewicht: 131.170 g/mol
• XLogP3: -1.700
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 131.095 Da
• Monoisotopic Mass: 131.095 Da
• Topological Polar Surface Area: 63.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 103.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1