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Molecule
ID:102661
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₁₃NO₂
Molecular Mass
131.17292
Exact Mass
131.09462866
Charge
0
InChI
InChI=1S/C6H13NO2/c1-2-3-4-5(7)6(8)9/h5H,2-4,7H2,1H3,(H,8,9)
InChIKey
LRQKBLKVPFOOQJ-UHFFFAOYSA-N
Canonic Smiles
CCCCC(C(=O)O)N
Isomeric Smiles
CCCCC(N)C(=O)O
Calculated Properties
JChem
LogD (pH = 7.4)
-1.43
LogD (pH = 5.5)
-1.43
Log P
-1.43
Rotatable Bonds
4
H Donor
2
H Acceptors
3
Lipinski's Rule of Five
true
Acid pKa
2.79
Polar Surface Area
63.32
Polarizability
14.38
Molar Refractivity
34.22
LOG S
-1.22
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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Quote
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
IUPAC Traditional name
•
Synonyms
•
IUPAC name
•
Brand Name
Registration numbers
Properties
•
Safety Information
•
Physical Property
•
Product Information
•
Pharmacology Properties
Related Proteins
Molecular Spectra
Molecule Details
•
Wikipedia
•
MP Biomedicals
•
ChEBI
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
InterBioScreen
BB_SC-8743
MP Biomedicals
02102482
Sigma Aldrich
N1398
74580
Enamine
EN300-18344
Bide Pharmatech
BD21800
Alfa Aesar
A10791
Academic Data
Wikipedia
Aminocaproic_acid
Norleucine
PubChem
9475
ChEBI
CHEBI:36405
Names and Identifiers
IUPAC Traditional name
2-aminohexanoic acid
norleucine
Synonyms
DL-NORLEUCINE
DL-2-Aminohexanoic acid
DL-2-Aminocaproic acid
Aminocaproic acid
Norleucine
Caprine
2-aminohexanoic acid
Glycoleucine
DL-正亮氨酸
(±)-2-Aminocaproic acid
DL-Norleucine
2-Aminohexanoic acid
H-DL-Nle-OH
(+/-)-2-Aminohexanoic acid
Nle
norleucine
IUPAC name
2-aminohexanoic acid
Brand Name
Amicar
Registration numbers
EC Number
210-462-7
CAS Number
616-06-8
60-32-2
327-57-1
CHEMBL
1046
Medline Plus
a608023
PubChem CID
564
9475
Chemspider ID
548
401917
Unique Ingredient Identifier
U6F3787206
832C8OV84S
CHEBI ID
16586
36405
CHEBI:36405
Wikipedia Title
Aminocaproic_acid
Norleucine
KEGG ID
D00160
C01933
DrugBank ID
DB00513
DB04419
ATC CODE
B02AA01
Beilstein Number
1721748
MeSH Name
Norleucine
Gmelin ID
464584
PubChem SID
24897485
162088716
24886697
14718110
MDL Number
MFCD00064422
Merck Index
146706
BKMS React Database
20457
21248
124284
21242
Patent number
WO2005063766
WO2005023838
GB1464774
US2006199822
WO2005092850
US2008249030
US2007238669
EP1586583
US2004248765
EP0922699
US2006264477
US2004002542
WO2007100535
EP1433778
WO2008142591
EP1323419
US2003220508
US2004171653
US2006094789
WO2007089665
US2006276628
US2002198378
EP1707200
US2006040974
EP1422218
US2005113368
US2004063771
US2004059120
US2008182889
US2002052422
US2003144342
EP1130022
US2006128963
US2005004043
WO2005007634
WO2005000298
US2006252813
US2008057127
US2003083267
US2006166895
WO2005080353
US2006020009
UniProt Database
Q766C2
P0DI89
P51124
P05041
P69477
Q05902
Q9BXF6
Q44297
P69476
Q03238
O57579
Q766C3
Q8MZS4
P00903
MetaboLights Database
MTBLS315
MTBLS328
MTBLS522
MTBLS653
MTBLS320
MTBLS215
MTBLS321
MTBLS411
MTBLS1040
BRENDA Ligand Database
21242
20457
21248
124284
Reaxys Registry
1721748
BRENDA Database
1.4.1.2
1.4.3.2
3.5.1.14
2.6.1.42
3.5.1.87
1.4.1.1
3.5.1.15
1.4.1.20
1.4.3.22
ACToR Database
327-57-1
616-06-8
NMRShiftDB Database
20096826
SureChEMBL Database
SCHEMBL8392
CompTox Database
DTXSID40861874
PubMed Citation Links
22770225
Molecule Details
Wikipedia
Aminocaproic_acid
Norleucine
MP Biomedicals
02102482
Purity: 98-99%
Crystalline
ChEBI
CHEBI:36405
An alpha-amino acid that is caproic acid substituted by an amino group at position 2.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
EC Number
•
CAS Number
•
CHEMBL
•
Medline Plus
•
PubChem CID
•
Chemspider ID
•
Unique Ingredient Identifier
•
CHEBI ID
•
Wikipedia Title
•
KEGG ID
•
DrugBank ID
•
ATC CODE
•
Beilstein Number
•
MeSH Name
•
Gmelin ID
•
PubChem SID
•
MDL Number
•
Merck Index
•
BKMS React Database
•
Patent number
•
UniProt Database
•
MetaboLights Database
•
BRENDA Ligand Database
•
Reaxys Registry
•
BRENDA Database
•
ACToR Database
•
NMRShiftDB Database
•
SureChEMBL Database
•
CompTox Database
•
PubMed Citation Links
Properties
Safety Information
Storage Condition
Room Temperature (15-30°C)
Source
MSDS Link
Download link
Source
Download link
Source
Safety Statements
36/37
Source
Risk Statements
43
Source
RTECS
RC6308000
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
TSCA Listed
是
Source
Physical Property
Melting Point
327°C
Source
301 °C (decomposes)
Source
>300 °C(lit.)
Source
300 - 302°C
Source
>300°C
Source
Density
1.17 g/ml
Source
p𝘒ₐ
2.39 (carboxyl), 9.76 (amino)
Source
16 g/l at 23 °C in water
Source
-1.537
Source
Product Information
Purity
98-99%
Source
≥99.0% (NT)
Source
95%
Source
98%
Source
Certificate of Analysis
Download link
Source
Grade
puriss.
Source
Linear Formula
CH3(CH2)3CH(NH2)COOH
Source
Pharmacology Properties
Metabolism
Renal
Source
Half Life
2 hours
Source
Solubility
Hydrophobicity(logP)