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Molecule
ID:126397
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₈N₂O₅
Molecular Mass
176.12742
Exact Mass
176.04332137
Charge
0
InChI
InChI=1S/C5H8N2O5/c6-5(12)7-2(4(10)11)1-3(8)9/h2H,1H2,(H,8,9)(H,10,11)(H3,6,7,12)
InChIKey
HLKXYZVTANABHZ-UHFFFAOYSA-N
Canonic Smiles
OC(=O)CC(C(=O)O)NC(=O)N
Isomeric Smiles
NC(=O)NC(CC(=O)O)C(=O)O
Calculated Properties
JChem
LogD (pH = 7.4)
-7.29
LogD (pH = 5.5)
-4.33
Log P
-1.74
Rotatable Bonds
4
H Donor
4
H Acceptors
5
Lipinski's Rule of Five
true
Acid pKa
3.33
Polar Surface Area
129.72
Polarizability
14.68
Molar Refractivity
34.65
LOG S
-0.07
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
No Data Available
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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
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Names and Identifiers
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Synonyms
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IUPAC name
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IUPAC Traditional name
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Physical Property
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
Wikipedia
Carbamoyl_aspartic_acid
PubChem
279
ChEBI
CHEBI:64850
Commercial Catalog
Sigma Aldrich
94290
Enamine
EN300-30856
Alfa Aesar
A17166
Names and Identifiers
Synonyms
Carbamoyl aspartic acid
Ureidosuccinic acid
N-Carbamoyl-DL-aspartic acid
N-氨基甲酰-DL-天冬氨酸
DL-脲基琥珀酸
2-[(aminocarbonyl)amino]succinic acid
N-Carbamoyl-DL-aspartic acid
Ureidosuccinic acid
氨基甲酰基-DL-天冬氨酸
Carbamoyl-DL-Asp-OH
Carbamylaspartic acid
N-carbamoylaspartic acid
N-(Aminocarbonyl)-DL-aspartic acid
2-Ureidobutanedioic acid
Ureidosuccinic acid
IUPAC name
2-(carbamoylamino)butanedioic acid
IUPAC Traditional name
ureidosuccinic acid
Registration numbers
Beilstein Number
1726861, 1726860
S
1726861
CHEBI ID
15859
CHEBI:64850
PubChem CID
279
CAS Number
923-37-5
CHEMBL
1161506
CHEMBL1161506
KEGG ID
C00438
DrugBank ID
DB04252
MeSH Name
ureidosuccinic+acid
Chemspider ID
273
Wikipedia Title
Carbamoyl_aspartic_acid
EC Number
213-096-6
PubChem SID
24889977
162220731
160645012
MDL Number
MFCD00042822
BRENDA Database
3.5.1.87
3.5.1.7
3.5.2.3
MetaboLights Database
MTBLS656
MTBLS3627
MTBLS2145
MTBLS8
MTBLS4722
MTBLS1282
MTBLS2295
MTBLS225
MTBLS2205
MTBLS3540
MTBLS3628
PubMed Citation Links
14367323
131912
13831
4550662
4610345
13882306
14920504
BKMS React Database
21640
136355
47951
BRENDA Ligand Database
136355
47951
21640
Reaxys Registry
1726859
SureChEMBL Database
SCHEMBL163119
SCHEMBL22718870
Molecule Details
Wikipedia
Carbamoyl_aspartic_acid
ChEBI
CHEBI:64850
An N-carbamoylamino acid that is aspartic acid with one of its amino hydrogens replaced by a carbamoyl group.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
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Beilstein Number
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CHEBI ID
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PubChem CID
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CAS Number
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CHEMBL
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KEGG ID
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DrugBank ID
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MeSH Name
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Chemspider ID
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Wikipedia Title
•
EC Number
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PubChem SID
•
MDL Number
•
BRENDA Database
•
MetaboLights Database
•
PubMed Citation Links
•
BKMS React Database
•
BRENDA Ligand Database
•
Reaxys Registry
•
SureChEMBL Database
Properties
Physical Property
p𝘒ₐ
3.649
Source
Partition Coefficient
-0.663
Source
p𝘒b
10.348
Source
Melting Point
~175 °C (dec.)
Source
ca 175°C dec.
Source
Hydrophobicity(logP)
-1.543
Source
Product Information
HOOCCH2CH(NHCONH2)COOH
Source
≥98.0%
Source
95%
Source
98%
Source
≤0.1%
Source
Safety Information
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Download link
Source
3
Source
否
Source
Linear Formula
Purity
Ignition Residue
Personal Protective Equipment
MSDS Link
German water hazard class
TSCA Listed