Basic information
- CAS
34994-11-1- Standard SMILES
NCC[C@H](O)CNCCCC[C@H](N)C(=O)O- InChIKey
BZUIJMCJNWUGKQ-IUCAKERBSA-N- Molecular formula
- C10H23N3O3
- Average molar mass
- 233.31 g/mol
- Monoisotopic mass
- 233.1739416
Names & identifiers
- Preferred name
- N~6~-[(2S)-4-amino-2-hydroxybutyl]-L-lysine
- IUPAC
- (2S)-2-amino-6-[[(2S)-4-amino-2-hydroxybutyl]amino]hexanoic acid
- English name
- hypusine
- Molecular formula
- C10H23N3O3
- Molecular weight
- 233.31
Names & synonyms
SCHEMBL167131LMFA01050514N~6~-[(2S)-4-amino-2-hydroxybutyl]-L-lysinehypusineL-Lysine, N6-[(2R)-4-amino-2-hydroxybutyl]-(2S)-2-aMino-6-[[(2S)-4-aMino-2-hydroxybutyl]aMino]hexanoic(2S)-2-aMino-6-[[(2S)-4-aMino-2-hydroxybutyl]aMino]hexanoic acid
Database identifiers
- CAS
34994-11-1- PubChem CID
- 65396
Properties
Computed structural properties
- XLogP
- -3.9
- Topological polar surface area
- 122 Ų
- Hydrogen bond donors
- 5
- Hydrogen bond acceptors
- 6
- Rotatable bonds
- 10
- Heavy atoms
- 16
- Formal charge
- 0
- Complexity
- 190
Experimental & physicochemical properties
LipidsFatty Acyls [FA] -> Fatty Acids and Conjugates [FA01] -> Hydroxy fatty acids [FA0105]
Physical DescriptionSolid
Physicochemical properties
- Boiling point
- 465.2 · 465.2±45.0 °C(Predicted)
- Density
- 1.151 · 1.151±0.06 g/cm3(Predicted)
- pka
- 2.5 · 2.50±0.24(Predicted)
- optical activity
- 2 S, · (2S, 9R)-:+9.916 (6 mol dm-3 HCl) (2S,9S)-:+1623 (6 mol dm-3 HCl)
- FDA UNII
- 3874 VXF092 · 3874VXF092
Chemistry & industry
Applications
UsesHypusine is a natural amino acid. The post-translational synthesis of hypusine is mainly catalyzed by deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxylase (DOHH)[1][2].
Suppliers4 total
上海陶术生物科技股份有限公司13564774135 · [email protected]
武汉佰乐博生物技术有限公司027-65279366 18108604356 · [email protected]
TargetMol中国（陶术生物）15002134094 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354 · [email protected]
Additional notes
DefinitionChEBI: An L-lysine derivative that is L-lysine bearing a (2R)-4-amino-2-hydroxybutyl substituent at position N6.
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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