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Norleucine

PubChem CID: 21236

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Compound Synonyms L-Norleucine, NORLEUCINE, 327-57-1, (S)-2-Aminohexanoic acid, H-Nle-OH, L-(+)-Norleucine, (2S)-2-aminohexanoic acid, Glycoleucine, Caprine, L-2-Aminohexanoate, L-2-Aminohexanoic acid, 2-Aminocaproic acid, Hexanoic acid, 2-amino-, (S)-, L-Aminohexanoate, alpha-Aminocaproic acid, Norleucine, L-, Norleucine (VAN), L(+)-Norleucine, (S)-(+)-2-Aminohexanoic acid, L-Aminohexanoic acid, NSC 10378, 2S-amino-hexanoic acid, (S)-2-Aminocaproic acid, (S)-Norleucine, EINECS 206-321-4, BRN 1721750, CHEBI:18347, 2-amino-hexanoic acid, 832C8OV84S, NORLEUCINE [MI], MFCD00064423, NSC-10378, DTXSID70883362, 4-04-00-02686 (Beilstein Handbook Reference), NLE, (S)-2-aminohexanoate, S-2-aminohexanoic acid, .alpha.-Aminocaproic acid, (S)-2-amino-Hexanoic acid, UNII-832C8OV84S, 2-Aminocaproate, 2-Aminohexanoate, (S)-Aminohexanoate, (S)-Aminohexanoic acid, H-Nle-OH L-Norleucine, (S)-2-amino-Hexanoate, (S)-2-aminohexanoicacid, hexanoic acid, 2-amino-, bmse000411, (2S)-2-azaniumylhexanoate, SCHEMBL8393, n-C4H9CH(NH2)COOH, N6877_SIGMA, CHEMBL292439, (S)-()-2-Aminohexanoic acid, L-Norleucine, >=98% (TLC), DTXCID201022899, 496-90-2, HY-Y0017, FD3031, LMFA01100042, AKOS006240047, CS-W020710, DB15458, FN46957, AC-22372, AS-13136, N0303, NS00074199, C01933, EN300-134822, M03242, L-2-Aminohexanoic acid, (S)-2-Aminocaproic acid, Q415428, B9CD20C9-2708-47D2-BEF1-0BA8BB0628AC, Z1203162297, L-Norleucine, suitable for amino acid analysis, BioReagent, 206-321-4
Topological Polar Surface Area 63.3
Hydrogen Bond Donor Count 2.0
Heavy Atom Count 9.0
Description An unnatural amino acid that is used experimentally to study protein structure and function. It is structurally similar to methionine, however it does not contain sulfur. Aminocaproic acid works as an antifibrinolytic. It is a derivative of the amino acid lysine. It binds reversibly to the kringle domain of plasminogen and blocks the binding of plasminogen to fibrin and its activation to plasmin. [HMDB]
Isotope Atom Count 0.0
Molecular Complexity 93.1
Database Name cmaup_ingredients;fooddb_chem_all;hmdb_chem_all;pubchem
Defined Atom Stereocenter Count 1.0
Iupac Name (2S)-2-aminohexanoic acid
Prediction Hob 1.0
Class Carboxylic acids and derivatives
Xlogp -1.5
Superclass Organic acids and derivatives
Subclass Amino acids, peptides, and analogues
Molecular Formula C6H13NO2
Prediction Swissadme 0.0
Inchi Key LRQKBLKVPFOOQJ-YFKPBYRVSA-N
Fcsp3 0.8333333333333334
Rotatable Bond Count 4.0
State Solid
Synonyms (S)-2-amino-Hexanoate, (S)-2-amino-Hexanoic acid, (S)-2-Aminohexanoate, (S)-2-Aminohexanoic acid, (S)-Aminohexanoate, (S)-Aminohexanoic acid, (S)-Norleucine, 2-Aminocaproate, 2-Aminocaproic acid, 2-Aminohexanoate, 2-Aminohexanoic acid, a-Aminocaproate, a-Aminocaproic acid, alpha-Aminocaproate, alpha-Aminocaproic acid, Caprine, Glycoleucine, L-(+)-Norleucine, L-2-Aminohexanoate, L-2-Aminohexanoic acid, L-Aminohexanoate, L-Aminohexanoic acid, L-Norleucine, L(+)-Norleucine, Nle, Norleucine, α-aminocaproate, α-aminocaproic acid, Α-aminocaproate, Α-aminocaproic acid, L-Isomer norleucine, Norleucine, L isomer, Norleucine, L-isomer, 2S-Amino-hexanoate
Substituent Name L-alpha-amino acid, Medium-chain fatty acid, Amino fatty acid, Fatty acyl, Fatty acid, Monocarboxylic acid or derivatives, Carboxylic acid, Hydrocarbon derivative, Primary amine, Organooxygen compound, Organonitrogen compound, Primary aliphatic amine, Carbonyl group, Amine, Aliphatic acyclic compound
Compound Name Norleucine
Kingdom Organic compounds
Prediction Hob Swissadme 0.0
Exact Mass 131.095
Formal Charge 0.0
Monoisotopic Mass 131.095
Hydrogen Bond Acceptor Count 3.0
Molecular Weight 131.17
Covalent Unit Count 1.0
Total Atom Stereocenter Count 1.0
Total Bond Stereocenter Count 0.0
Molecular Framework Aliphatic acyclic compounds
Esol 0.5809150000000004
Inchi InChI=1S/C6H13NO2/c1-2-3-4-5(7)6(8)9/h5H,2-4,7H2,1H3,(H,8,9)/t5-/m0/s1
Smiles CCCC[C@@H](C(=O)O)N
Defined Bond Stereocenter Count 0.0
Taxonomy Direct Parent L-alpha-amino acids

  • 1. Outgoing r'ship FOUND_IN to/from Pogostemon Cablin (Plant) Rel Props:Source_db:cmaup_ingredients