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Molecule
ID:2844
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₁₄N₄O₃
Molecular Mass
190.20036
Exact Mass
190.10659033
Charge
0
InChI
InChI=1S/C6H14N4O3/c7-4(5(11)12)2-1-3-9-6(8)10-13/h4,13H,1-3,7H2,(H,11,12)(H3,8,9,10)/t4-/m0/s1
InChIKey
FQWRAVYMZULPNK-BYPYZUCNSA-N
Canonic Smiles
ONC(=N)NCCC[C@@H](C(=O)O)N
Isomeric Smiles
N[C@@H](CCCNC(=N)NO)C(=O)O
Calculated Properties
JChem
Acid pKa
2.1966505
H Acceptors
7
H Donor
6
LogD (pH = 5.5)
-6.004631
LogD (pH = 7.4)
-4.778636
Log P
-3.2532802
Molar Refractivity
66.1805
Polarizability
17.59352
Polar Surface Area
131.46
Rotatable Bonds
5
Lipinski's Rule of Five
false
ALOGPS 2.1
Log P
-3.57
LOG S
-2.1
Solubility (Water)
1.49e+00 g/l
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
•
RDKit
•
JChem
•
ALOGPS 2.1
Data Source
•
Academic Data
Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
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PubChem CID
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PubChem SID
Properties
Related Proteins
Molecular Spectra
Molecule Details
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DrugBank
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Academic Data
DrugBank
DB03144
PubChem
123895
Names and Identifiers
IUPAC name
(2S)-2-amino-5-(1-hydroxycarbamimidamido)pentanoic acid
Synonyms
N-Omega-Hydroxy-L-Arginine
IUPAC Traditional name
(2S)-2-amino-5-(1-hydroxycarbamimidamido)pentanoic acid
Registration numbers
PubChem CID
123895
PubChem SID
160966291
46506099
Molecule Details
DrugBank
DB03144
Drug information: experimental
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay