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Molecule
ID:119241
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₁₂N₂O₄
Molecular Mass
176.17048
Exact Mass
176.07970687
Charge
0
InChI
InChI=1S/C6H12N2O4/c1-3(7)5(10)8-4(2-9)6(11)12/h3-4,9H,2,7H2,1H3,(H,8,10)(H,11,12)/t3-,4-/m0/s1
InChIKey
IPWKGIFRRBGCJO-IMJSIDKUSA-N
Canonic Smiles
OC[C@@H](C(=O)O)NC(=O)[C@@H](N)C
Isomeric Smiles
N(C(=O)[C@@H](N)C)[C@H](C(=O)O)CO
Calculated Properties
JChem
Acid pKa
3.476462
H Acceptors
5
H Donor
4
LogD (pH = 5.5)
-4.4276805
LogD (pH = 7.4)
-4.463853
Log P
-4.426506
Molar Refractivity
39.3384
Polarizability
15.829292
Polar Surface Area
112.65
Rotatable Bonds
4
Lipinski's Rule of Five
true
Data Source
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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
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RDKit
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JChem
Data Source
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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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CAS Number
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MDL Number
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PubChem CID
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PubChem SID
Properties
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
InterBioScreen
BB_NC-0544
Sigma Aldrich
A3503
Academic Data
PubChem
1549433
Names and Identifiers
IUPAC name
(2S)-2-[(2S)-2-aminopropanamido]-3-hydroxypropanoic acid
Synonyms
Ala-Ser
(S)-2-((S)-2-aminopropanamido)-3-hydroxypropanoic acid
IUPAC Traditional name
(2S)-2-[(2S)-2-aminopropanamido]-3-hydroxypropanoic acid
Registration numbers
CAS Number
3303-41-1
MDL Number
MFCD00066028
PubChem CID
1549433
PubChem SID
162102868
Properties
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay