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Molecule
ID:107458
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₃NO₆
Molecular Mass
267.23472
Exact Mass
267.07428714
Charge
0
InChI
InChI=1S/C12H13NO6/c14-10(15)6-9(11(16)17)13-12(18)19-7-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,13,18)(H,14,15)(H,16,17)/t9-/m1/s1
InChIKey
XYXYXSKSTZAEJW-SECBINFHSA-N
Canonic Smiles
O=C(N[C@@H](C(=O)O)CC(=O)O)OCc1ccccc1
Isomeric Smiles
OC(=O)C[C@@H](NC(=O)OCc1ccccc1)C(=O)O
Calculated Properties
JChem
Acid pKa
3.4672694
H Acceptors
5
H Donor
3
LogD (pH = 5.5)
-1.5431607
LogD (pH = 7.4)
-4.6141987
Log P
0.94208765
Molar Refractivity
62.2127
Polarizability
24.478523
Polar Surface Area
112.93
Rotatable Bonds
7
Lipinski's Rule of Five
true
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
No Data Available
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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 Traditional name
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IUPAC name
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Synonyms
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Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
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TRC
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
MP Biomedicals
05203815
Sigma Aldrich
95965
TRC
C176280
Bide Pharmatech
BD22617
Academic Data
PubChem
5289152
Names and Identifiers
IUPAC Traditional name
(2R)-2-{[(benzyloxy)carbonyl]amino}butanedioic acid
IUPAC name
(2R)-2-{[(benzyloxy)carbonyl]amino}butanedioic acid
Synonyms
CARBOBENZOXY-D-ASPARTIC ACID
Z-D-aspartic acid
Z-D-天冬氨酸
Z-D-Asp-OH
Z-D-Asp-OH
N-Carbobenzyloxy-D-aspartic Acid
Registration numbers
CAS Number
78663-07-7
PubChem SID
162093456
24890226
PubChem CID
5289152
MDL Number
MFCD00063182
Beilstein Number
2566464
Molecule Details
MP Biomedicals
05203815
MP Biomedicals Rare Chemical collection
Sigma Aldrich
95965
Packaging
5 g in poly bottle
TRC
C176280
A competitive inhibitor of indole-3-acetyl-L-aspartic acid hydrolase of Enterobacter agglomerans.
References
PubChem Literature
From Data Sources
•
Chou, J., et al.: Plant Physiol., 112, 1281 (1988)
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Szerszen, J., et al.: Science, 265, 1699 (1988)
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Jackson, R., et al.: J. Biol. Chem., 276, 4350 (1988)
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Glass, N., et al.: J. Bacteriol., 170, 2367 (1988)
Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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PubChem SID
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PubChem CID
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MDL Number
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Beilstein Number
Properties
Safety Information
MSDS Link
Download link
Source
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Source
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Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
Refrigerator
Source
Product Information
Download link
Source
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Source
C12H13NO6
Source
≥98.0%
Source
95+%
Source
Physical Property
110-112°C
Source
Methanol
Source
Off-White Solid
Source
Storage Condition
Certificate of Analysis
Empirical Formula (Hill Notation)
Purity
Melting Point
Solubility
Apperance