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Molecule
ID:3480
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₁NO₃
Molecular Mass
181.18854
Exact Mass
181.07389322
Charge
0
InChI
InChI=1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m1/s1
InChIKey
OUYCCCASQSFEME-MRVPVSSYSA-N
Canonic Smiles
OC(=O)[C@@H](Cc1ccc(cc1)O)N
Isomeric Smiles
N[C@H](Cc1ccc(O)cc1)C(=O)O
Calculated Properties
JChem
LogD (pH = 7.4)
-1.50
LogD (pH = 5.5)
-1.49
Log P
-1.49
Rotatable Bonds
3
H Donor
3
H Acceptors
4
Lipinski's Rule of Five
true
Acid pKa
2.00
Polar Surface Area
83.55
Polarizability
18.06
Molar Refractivity
47.10
LOG S
-0.98
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
No Data Available
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Molecule Details
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References
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Bioactivity
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Quote
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Navigation
General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Academic Data
•
Commercial Catalog
Names and Identifiers
•
IUPAC Traditional name
•
Synonyms
•
IUPAC name
Registration numbers
Properties
•
Safety Information
•
Product Information
•
Physical Property
Related Proteins
•
PDB Bank
Molecular Spectra
Molecule Details
•
DrugBank
•
MP Biomedicals
•
Sigma Aldrich
•
ChEBI
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Academic Data
DrugBank
DB03839
PubChem
71098
ChEBI
CHEBI:28479
Commercial Catalog
MP Biomedicals
02103175
Sigma Aldrich
855456
93840
Bide Pharmatech
BD34088
Alfa Aesar
A17709
Names and Identifiers
IUPAC Traditional name
(.+-.)-tyrosine
Synonyms
D-3-[4-Hydroxyphenyl]alanine
D-2-Amino-3-(4-hydroxyphenyl)propionic acid
3-(4-Hydroxyphenyl)-D-alanine
D-Tyrosine
(R)-2-Amino-3-(4-hydroxyphenyl)propionic acid
D-Tyrosine
D-酪氨酸
3-(4-羟基苯基)-D-丙氨酸
(R)-2-氨基-3-(4-羟基苯基)丙酸
D-酪胺酸
H-D-Tyr-OH
(R)-3-(p-Hydroxyphenyl)alanine
(R)-2-Amino-3-(p-hydroxyphenyl)propionic acid
D-tyrosine
D-TYROSINE
(2R)-2-amino-3-(4-hydroxyphenyl)propanoic acid
D-Tyrosin
DTY
D-Tyrosine
D-Tyr
IUPAC name
(2R)-2-amino-3-(4-hydroxyphenyl)propanoic acid
Related Proteins
PDB Bank
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7KNG
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5KGN
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5XPK
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6XS8
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5GO8
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6Y0W
6KZF
1ZEA
5GOJ
5GOK
7KJM
1OF6
6Q86
6XS5
7KJN
6PHN
6PSA
7BAG
2R5B
3TPX
3L37
6LYC
6Q8D
7BPH
3L35
5LY2
7RIH
7RMS
3RUL
5GOH
2IH0
4OIJ
6Q87
5N8J
3GO0
2Q33
6JV7
3LNJ
5I5B
6Q6X
6YW4
1C4B
3L36
5E5Y
6YW1
5GOG
2H9E
5HHC
5KEZ
4GLU
7LL9
1D7T
7RMQ
6S5R
5E4N
5XDP
5JBV
5I5A
2LA0
6PHM
6WGN
7LL8
4GLN
5GOB
6X5I
2IGZ
3UE7
2R5D
6L63
5NGQ
6Q8H
1XA0
6Q85
5J8P
5JBY
6PHQ
6Y0X
4GLS
5E40
5GO7
7KNF
5HHD
6KZU
7E5E
3FHV
5X3O
6Q79
6YW3
1UNO
6YW2
5GOI
5GOC
5E5T
6Q6W
6XS7
7RIJ
7RNW
5GOD
7RMR
7L4Z
5X3M
4OIK
5LY1
6BES
Molecule Details
DrugBank
DB03839
Drug Groups
experimental
Description
A non-essential amino acid. In animals it is synthesized from PHENYLALANINE. It is also the precursor of EPINEPHRINE; THYROID HORMONES; and melanin. [PubChem]
MP Biomedicals
02103175
Crystalline
Purity: 98.5% min.
Sigma Aldrich
855456
Packaging
5 g in glass bottle
500 mg in glass bottle
Legal Information
ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC
ChEBI
CHEBI:28479
An optically active form of tyrosine having D-configuration.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
PubChem SID
•
PubChem CID
•
MDL Number
•
Beilstein Number
•
EC Number
•
Merck Index
•
Protein Data Bank
•
MetaboLights Database
•
UniProt Database
•
PubMed Citation Links
•
Reaxys Registry
•
MetaCyc Database
•
BKMS React Database
•
CHEBI ID
•
CompTox Database
•
Patent number
•
KEGG ID
•
SABIO-RK Database
•
SureChEMBL Database
•
DrugBank ID
•
BindingDB Database
•
Gmelin ID
•
BRENDA Ligand Database
•
ECMDB Database
•
PDBeChem Database
•
CHEMBL
•
YMDB Database
Registration numbers
CAS Number
556-02-5
PubChem SID
160966919
46504669
24889933
24888381
8144339
PubChem CID
71098
6057
MDL Number
MFCD00063073
Beilstein Number
2212157
EC Number
209-112-6
Merck Index
149839
Protein Data Bank
7kng
5kgn
5xpk
6xs8
5go8
6y0w
6kzf
1zea
5goj
5gok
7kjm
1of6
6q86
6xs5
7kjn
6phn
MetaboLights Database
MTBLS2096
MTBLS379
MTBLS1693
UniProt Database
Q0BP79
B3E9B8
P44814
A1ALA7
Q7N9S2
Q124Q1
Q4L6X8
B7HQG5
B4SKG5
A9MIA3
B7LVG2
Q39JJ5
Q2SZ60
B7GUW9
Q8NP96
PubMed Citation Links
24936396
23381872
15292242
Reaxys Registry
2212157
MetaCyc Database
D-TYROSINE
BKMS React Database
1643
2139
110
CHEBI ID
CHEBI:28479
CHEBI:21111
CHEBI:4258
CHEBI:42299
CompTox Database
DTXSID50883441
Patent number
EP1657249
US2006276628
US2005154185
EP1870419
US2005187284
US2004034080
EP1749815
EP1586583
KEGG ID
C06420
SABIO-RK Database
7656
7902
12891
9717
16030
SureChEMBL Database
SCHEMBL20787
DrugBank ID
DB03839
BindingDB Database
50463198
Gmelin ID
603524
BRENDA Ligand Database
1643
2139
110
ECMDB Database
ECMDB21520
PDBeChem Database
DTY
CHEMBL
CHEMBL1076637
YMDB Database
YMDB00805
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Storage Condition
Room Temperature (15-30°C)
Source
Safety Statements
26
-
36
Source
26
-
37
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
German water hazard class
3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Signal Word
Warning
Source
Risk Statements
36/37/38
Source
TSCA Listed
是
Source
Product Information
Purity
98.5%
Source
99%
Source
≥99.0% (NT)
Source
98%
Source
Certificate of Analysis
Download link
Source
Linear Formula
4-(HO)C6H4CH2CH(NH2)CO2H
Source
ReagentPlus®
Source
puriss.
Source
ee: 99% (GLC)
Source
Physical Property
Optical Rotation
[α]20/D +10.3°, c = 5 in 1 M HCl
Source
[α]20/D +11.5±1.0°, c = 4% in 1 M HCl
Source
+11 (c=4 in 1N HCl)
Source
Melting Point
>300 °C(lit.)
Source
310-314°C
Source
6psa
7bag
2r5b
3tpx
3l37
6lyc
6q8d
7bph
3l35
5ly2
7rih
7rms
3rul
5goh
2ih0
4oij
6q87
5n8j
3go0
2q33
6jv7
3lnj
5i5b
6q6x
6yw4
1c4b
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5e5y
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2h9e
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6s5r
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7ll8
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5gob
6x5i
2igz
3ue7
2r5d
6l63
5ngq
6q8h
1xa0
6q85
5j8p
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6y0x
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5go7
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6kzu
7e5e
3fhv
5x3o
6q79
6yw3
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6yw2
5goi
5goc
5e5t
6q6w
6xs7
7rij
7rnw
5god
7rmr
7l4z
5x3m
4oik
5ly1
6bes
A0LQX9
A7GHS6
B7GQ87
A3MP68
B3QL07
A6LTN7
Q11RA1
B1VDF7
Q96YQ2
A7GT88
Q3JD71
C1CSR0
A1WW09
A9B6D5
Q2FG94
Q04AV5
Q46AI3
A4JBK9
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Q9RVY1
B3QTV8
C1FKE9
P58852
B7I245
A0RJ14
B7JPZ2
A8H9H9
Q3YV89
A4G1U1
P63997
Q67LN1
Q5H5B9
Q9CJ92
Q49Y71
Q9K4F6
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Q1J4K7
B7VHE8
B2HD97
A3CZD8
B0VP57
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B2UQS5
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A4XI81
B3DQN7
Q9K143
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A4W4G5
A6TG77
A9R655
B0K971
B7V3H2
Q1JEU0
B8E1C2
Q3JNS1
C1CUI9
C4LJ12
O66742
B2SYK5
B2AH66
Q97GU2
A1V060
Q5V452
Q97PH3
B2TVN1
A6U2A1
Q81LI3
Q38XN8
B2FIQ2
Q9KNJ7
C1APH7
A1SB48
B1Y9H2
A6TQP0
A4VY70
Q2FXU2
A2RGJ5
Q8RGF0
Q5KWS4
B2V7S8
A8Z2G0
Q3IJ42
Q8Y239
A1K1M2
Q47K67
A8AL53
B1L0A0
C6BS14
A9WE39
A6VL72
Q9HM47
Q5WHP9
Q74FT1
A7FCQ4
Q74IX3
A2BKX3
A6UP03
Q04HP9
Q32A57
Q5QV32
B2RM63
Q9HUA4
A5VJG2
Q8RAL7
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A3DLP6
A3MWS2
A9BUE9
B0BZ98
A1BI65
C3KTC0
Q2T9V8
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C1CLY4
A0LY87
A1JHU4
Q1IHZ8
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A5F4Q7
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B7N2M8
B1XB55
P0A028
Q1GAH0
Q54088
A4XPL8
A0PSA3
B7UNK4
C0Q3J4
P0A6M5
B0KM52
P0DA80
Q6AS26
A1TYQ0
B1MIM7
A7Z754
Q2P814
C3L611
Q5LIY8
A2STU3
Q9KDH0
Q65GR0
B1KLY5
B9KAP7
B8FQT8
A2SKK9
P58533
C5CGW6
Q4KJM7
C5CM14
C1C8N4
B7M686
B6I4M4
B8G857
A8MGN0
C6DYE1
Q07648
Q1CN42
A9VIN2
A1A216
Q0HNG8
Q2LTS7
A9GKM6
B9DNG1
Q02ET8
Q8DDS3
A4J2H0
P63996
B7MI18
Q2S3D4
C5A055
Q6F6W0
Q8ZVE0
A6GW89
Q8DNX2
B7HE40
Q634D8
Q47KR7
C1DAD5
Q5LP58
A5EVP7
B1JR03
Q475S4
Q5JH30
Q5Z1P0
B8CHJ7
Q4UQ26
A6SUP6
A6UUZ4
A3QIW0
B9M4M9
A5UE61
B1XM75
B7IDL6
P84066
Q043X5
B0K0N1
A7NLC3
B1YJF9
Q7MQ06
Q1R431
Q63QX1
A1WC42
C1ESV0
C0QT00
B9IYY0
Q12IK4
A6VDK2
B1HV77
B7NUY4
Q6G8T6
B1VS48
Q1Q8K9
Q71ZE8
Q1DDE5
A8GLH9
A0AIX1
A9MZA2
Q3ZAH5
Q8KBF6
Q0TP24
Q8TEA8
A5N1Z2
Q4JCK7
A8FFP8
Q0HQC0
A4IR99
Q8G4Q2
A5ITF7
Q1JJU8
Q3JZ09
B1L7X6
Q72C32
B5F000
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C1KVG9
B9L8Z4
B3H319
B0R384
C4KJG8
Q8XJ24
Q489A4
C5C226
P0DA81
B8CXE9
Q9CKK0
B8ZM41
B0TW90
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B2G6X7
A4VGD5
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A1TDH1
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Q5E8Q0
A8LJ36
A1RS86
B6EGQ6
Q183H9
A8MCV2
Q48R77
Q2SN53
A1B2U5
Q3A002
C3MJC8
A7IAL9
B8GIX8
A0KRY8
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B5FFD2
A1KJW2
A4WGB6
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B5YZ24
B1IME1
B1JVU9
Q97CM5
Q892A9
Q9V2R8
A0Q402
Q31UA6
Q6C7S6
Q8CP01
C5BPU7
A5GC79
Q28NX0
A1VJK0
Q2YT97
A6QHH5
B3WEN3
P63999
P0A6M6
P58532
Q57630
A5UHF9
Q5HFD0
P58850
Q730C6
B1I710
A5FMN0
Q8P4H1
C1B035
Q3J474
Q0S3F3
B5FP17
A0LL48
A6LML3
Q4FQD6
A1VDX8
B9MCH0
A9AH76
A5FSN9
Q7NYM3
Q68EL2
A8ABM7
B5XZI4
P63998
Q1I3R4
Q54235
B9KPE1
A8ZUJ9
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A8A6Y8
B8E4B8
A9KXA7
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Q8EPR6
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A4J0B0
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A1T099
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Q5F6A6
A5WH93
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B1YTD6
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B9ML29
B8FHU4
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B5RFE5
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B2JGU7
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B7K3F6
B0BTX7
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B4EET1
B8J080
B2I1P4
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B2TN01
Q9DD18
Q2IMC5
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Q9JST7
Q5M1S1
Q4QMP6
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Q3BNL9
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B4RNL5
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B5XIM6
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A9BIE9
Q2FPX3
B5EAS6
C3K814
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B0S1I7
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B1ZZ94
A0R080
A5IJ55
B8GU25
Q1IY72
A5I6D9
A3DF46
B6YSX3
Q8FPG8
B3EG59
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Q817X5
B0TPR8
Q66GF4
Q6CRI9
C1DHT6
B7IIR8
A0B5C3
B8DSS1
B2GBW6
Q033A2
B4U592
Q31JB0
B5YDT2
B1LMS1
B2VFA6
B9E709
Q1GFL4
Q3A9Z9
A3N3P1
B2V347
Q0SRP4
Q75E22
C5A422
Q9HS70
A8FPZ5
C6DJD2
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C0ZAQ1
A7FY07
A4WL31
B7KKT8
A0RUG0
B8D4Z8
B0TF85
Q6DB68
A7X347
Q6GG71
B2JYL4
B2GIA9
Q1WTX9
C4L8J8
A4T8S3
Q220S3
Q0BI86
B1I337
A9KK74
A1REM9
Q03SF0
Q8PS92
A6VFS5
Q6L1F5
A6KZN7
A4Y2G8
Q0SZ73
Q5X472
Q88D02
Q21NB9
Q65WM2
Q2NQS5
P0A026
Q48PK8
Q1ATQ8
A5U3R6
Q7MTG7
Q24UQ3
A6VT94
Q038Q9
A5WA61
B7L9D6
B5BJ27
Q5PKE2
B4TPN8
Q73ZI0
A6WI48
C5BC71
C5CCH1
B7NFI6
C4Z1C2
Q0TAH5
C4L533
O14274
Grade
Optical Purity