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Molecule
ID:18419
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₃NO₃
Molecular Mass
195.21512
Exact Mass
195.08954328
Charge
0
InChI
InChI=1S/C10H13NO3/c1-14-10(13)9(11)6-7-2-4-8(12)5-3-7/h2-5,9,12H,6,11H2,1H3/t9-/m0/s1
InChIKey
MWZPENIJLUWBSY-VIFPVBQESA-N
Canonic Smiles
COC(=O)[C@H](Cc1ccc(cc1)O)N
Isomeric Smiles
C(=O)([C@H](Cc1ccc(cc1)O)N)OC
Calculated Properties
JChem
LogD (pH = 7.4)
0.84
LogD (pH = 5.5)
-0.29
Log P
0.92
Rotatable Bonds
4
H Donor
2
H Acceptors
3
Lipinski's Rule of Five
true
Acid pKa
6.69
Polar Surface Area
72.55
Polarizability
20.29
Molar Refractivity
51.87
LOG S
-1.19
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
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
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IUPAC Traditional name
•
IUPAC name
•
Synonyms
Registration numbers
Properties
•
Safety Information
•
Product Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
MP Biomedicals
•
Sigma Aldrich
•
TRC
•
ChEBI
References
•
PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
05223166
Matrix Scientific
020549
Sigma Aldrich
T90808
93920
TRC
M332525
Bide Pharmatech
BD12188
Academic Data
PubChem
70652
ChEBI
CHEBI:17215
Names and Identifiers
IUPAC Traditional name
tyrosine methyl ester
IUPAC name
methyl (2S)-2-amino-3-(4-hydroxyphenyl)propanoate
Synonyms
(S)-2-Amino-3-(4-hydroxy-phenyl)-propionic acid methyl ester
H-Tyr-OMe
L-Tyrosine Methyl Ester
L-TYROSINE-C-METHYL ETHER
Methyl L-Tyrosinate
Methyl Tyrosinate
Methyl (2S)-2-Amino-3-(4-hydroxyphenyl)propionate
(S)-2-Amino-3-(4-hydroxyphenyl)propionic Acid Methyl Ester
L-Tyrosine methyl ester
L-酪氨酸甲酯
L-Tyrosine methyl ester
methyl L-tyrosinate
Tyr-OMe
Tyrosine methyl ester
2-Amino-3-(4-hydroxy-phenyl)-propionic acid methyl ester
L-tyrosine methyl ester
Registration numbers
MDL Number
MFCD00002392
EC Number
214-095-3
CAS Number
1080-06-4
PubChem CID
70652
PubChem SID
160981726
24900583
8144244
Beilstein Number
2372626
BKMS React Database
68153
4828
15040
33276
61194
21854
114619
12720
Patent number
US2006154970
EP1591440
CompTox Database
DTXSID40148354
HMDB Database
HMDB0029217
BRENDA Database
1.4.3.2
4.3.1.25
2.8.2.22
3.4.11.24
2.8.2.2
3.1.1.43
2.3.1.110
1.14.18.1
2.8.2.9
3.1.1.73
BRENDA Ligand Database
21854
33276
114619
12720
4828
61194
68153
15040
CHEBI ID
CHEBI:17215
CHEBI:185566
CHEBI:6314
CHEBI:13182
CHEBI:21413
PubMed Citation Links
3656360
24434201
12459019
8385625
MetaboLights Database
MTBLS1622
MTBLS36
MTBLS1693
MTBLS2825
MTBLS2295
MTBLS2559
MTBLS459
MTBLS2878
MTBLS2096
MTBLS4012
MTBLS4463
UniProt Database
P84516
IntEnz Database
EC 2.8.2.9
Reaxys Registry
2372626
KEGG ID
C03404
ACToR Database
1080-06-4
CHEMBL
CHEMBL300797
SureChEMBL Database
SCHEMBL314923
Rhea Database
RHEA:19977
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
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Source
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Source
Download link
Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
German water hazard class
3
Source
Storage Temperature
2-8°C
Source
-20°C
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Product Information
Certificate of Analysis
Download link
Source
Download link
Source
Linear Formula
4-(HO)C6H4CH2CH(NH2)COOCH3
Source
Purity
98%
Source
≥99.0% (NT)
Source
95+%
Source
Grade
puriss.
Source
Physical Property
Optical Rotation
[α]20/D +26°, c = 2.4 in methanol
Source
[α]20/D +27±1°, c = 4% in methanol
Source
Melting Point
134-136 °C(lit.)
Source
134-136 °C
Source
Solubility
Chloroform
Source
Methanol
Source
Ethyl Acetate
Source
Apperance
White Solid
Source
Molecule Details
MP Biomedicals
05223166
MP Biomedicals Rare Chemical collection
Sigma Aldrich
T90808
Packaging
25 g in poly bottle
5 g in glass bottle
TRC
M332525
L-Tyrosine-induced antinociception is mediated by central .delta.-opioid receptors and by the bulbo-spinal noradrenergic system.
ChEBI
CHEBI:17215
An L-tyrosyl ester that is the methyl ester of L-tyrosine.
References
PubChem Literature
From Data Sources
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Zhang, D., et al.: J. Biotechnol., 128, 788 (1993)
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11) Watanabe, T., et al.: Life Sci., 54, 369 (1993)
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Kawabata, A., et al.: Eur. J. Pharma., 233, 255 (1993)
Bioactivity
PubChem BioAssay
Registration numbers
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MDL Number
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EC Number
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CAS Number
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PubChem CID
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PubChem SID
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Beilstein Number
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BKMS React Database
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Patent number
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CompTox Database
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HMDB Database
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BRENDA Database
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BRENDA Ligand Database
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CHEBI ID
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PubMed Citation Links
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MetaboLights Database
•
UniProt Database
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IntEnz Database
•
Reaxys Registry
•
KEGG ID
•
ACToR Database
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CHEMBL
•
SureChEMBL Database
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Rhea Database