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Molecule
ID:132931
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₃H₁₉N₂NaO₅
Molecular Mass
426.39713
Exact Mass
426.119166
Charge
0
InChI
InChI=1S/C23H20N2O5.Na/c26-19-12-6-15(7-13-19)14-20(25-21(27)16-4-2-1-3-5-16)22(28)24-18-10-8-17(9-11-18)23(29)30;/h1-13,20,26H,14H2,(H,24,28)(H,25,27)(H,29,30);/q;+1/p-1/t20-;/m0./s1
InChIKey
HEJYVLSWQWPKPQ-BDQAORGHSA-M
Canonic Smiles
O=C([C@@H](NC(=O)c1ccccc1)Cc1ccc(cc1)O)Nc1ccc(cc1)C(=O)[O-].[Na+]
Isomeric Smiles
c1ccc(cc1)C(=O)N[C@@H](Cc1ccc(cc1)O)C(=O)Nc1ccc(cc1)C(=O)[O-].[Na+]
Calculated Properties
JChem
Acid pKa
4.157471
H Acceptors
5
H Donor
3
LogD (pH = 5.5)
2.1798987
LogD (pH = 7.4)
0.47363257
Log P
3.5389557
Molar Refractivity
123.5821
Polarizability
41.927135
Polar Surface Area
118.56
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
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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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Synonyms
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IUPAC Traditional name
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IUPAC name
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Physical Property
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Molecular Spectra
Molecule Details
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Sigma Aldrich
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
Sigma Aldrich
B0262
13135
Academic Data
PubChem
23680486
Names and Identifiers
Synonyms
N-Benzoyl-L-tyrosyl-4-aminobenzoic acid sodium salt
Bentiromide
N-Benzoyl-L-tyrosine p-amidobenzoic acid sodium salt
IUPAC Traditional name
sodium 4-[(2S)-3-(4-hydroxyphenyl)-2-(phenylformamido)propanamido]benzoate
IUPAC name
sodium 4-[(2S)-3-(4-hydroxyphenyl)-2-(phenylformamido)propanamido]benzoate
Registration numbers
CAS Number
41748-47-4
MDL Number
MFCD00042647
EC Number
255-530-7
PubChem SID
162227208
24848007
PubChem CID
23680486
Molecule Details
Sigma Aldrich
13135
Other Notes
Hydrolysis of benzol-tyrosyl-p-aminobenzoic acid by a human intestinal microvillar peptidase1; Substrate for the assay of chymotrypsin in crude biological materials.2
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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MDL Number
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EC Number
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PubChem SID
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PubChem CID
Properties
Safety Information
Storage Temperature
-20°C
Source
2-8°C
Source
European Hazard Symbols
Irritant (Xi)
Source
36/38
Source
1
Source
3
Source
26
-
36
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Download link
Source
Physical Property
powder
Source
[α]20/D +45±2°, c = 1% in DMF/H2O 1:1
Source
~210 °C (dec.)
Source
Product Information
≥98.0% (sum of enantiomers, HPLC)
Source
C23H19N2O5Na
Source
lyophilized
Source
Risk Statements
German water hazard class
Safety Statements
Personal Protective Equipment
MSDS Link
Apperance
Optical Rotation
Melting Point
Purity
Linear Formula
Quality