Molfinder
主页
技术支持
关于我们
数据来源
数据统计
博客
Molecule
ID:128004
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₃H₆O₂
Molecular Mass
74.07854
Exact Mass
74.03677943
Charge
0
InChI
InChI=1S/C3H6O2/c1-3(5)2-4/h2-3,5H,1H3
InChIKey
BSABBBMNWQWLLU-UHFFFAOYSA-N
Canonic Smiles
CC(C=O)O
Isomeric Smiles
O=CC(O)C
Calculated Properties
JChem
LogD (pH = 7.4)
-0.63
LogD (pH = 5.5)
-0.63
Log P
-0.63
Rotatable Bonds
1
H Donor
1
H Acceptors
2
Lipinski's Rule of Five
true
Acid pKa
14.01
Polar Surface Area
37.30
Polarizability
7.17
Molar Refractivity
17.91
LOG S
0.57
Data Source
Loading...
Names and Identifiers
Loading...
Registration numbers
Loading...
Properties
No Data Available
Click here to submit data
Related Proteins
No Data Available
Click here to submit data
Molecular Spectra
No Data Available
Click here to submit data
Molecule Details
Loading...
References
Loading...
Bioactivity
Loading...
Quote
Download
Navigation
General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC Traditional name
•
IUPAC name
Registration numbers
Properties
Related Proteins
Molecular Spectra
Molecule Details
•
Wikipedia
•
ChEBI
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Academic Data
PubChem
855
Wikipedia
Lactaldehyde
ChEBI
CHEBI:18419
Names and Identifiers
Synonyms
Lactaldehyde
Hydroxypropionaldehyde
2-hydroxypropionaldehyde
2-Hydroxypropionaldehyde
2-Hydroxypropanal
lactaldehyde
Lactaldehyde
IUPAC Traditional name
lactaldehyde
IUPAC name
2-hydroxypropanal
Registration numbers
Chemspider ID
832
KEGG ID
C05999
Wikipedia Title
Lactaldehyde
PubChem CID
855
CHEBI ID
18419
CHEBI:24994
CHEBI:6349
CHEBI:11015
CHEBI:18419
CAS Number
598-35-6
PubChem SID
162222320
8143764
ACToR Database
3913-65-3
UniProt Database
Q926R2
Q32A68
B2K1W0
A9MZC4
Q8X8A1
Q65Q26
A8A2B1
B7N5L0
Q8Z549
A7ZQP6
B5QWR0
Q58806
B7UHL8
B5XUY5
A4WG94
B5XZ54
A1AI79
P32169
P83775
B7M6V4
B5QWY1
B7LXL8
Q8FEE7
A9N2J1
B4TBY0
B5R262
Q3YZW1
A6VGC7
Q04I16
P0A9S5
B4SZZ0
Q9RQ13
A8AP13
Q12068
O32210
B6I4P4
A9N5C4
P69922
Q1R7N8
B7LVE1
B7MXS6
Q32CB6
Q5PI50
C1CB02
B1LMU2
B5FP38
B4TPQ6
Q8ZKS1
B7NUA6
Q1C0V7
B1IVH6
Q31Z78
P44399
B5FTY1
C5A070
P69923
B1I9W8
B5Z4C2
Q8DN24
C4ZZV7
B4T4X1
A6VH72
B5BJG5
B5EZG8
C6DJR1
C0Q079
B7NVV0
P44779
A6TD83
A7ML62
B7MI34
A6TBU6
B2INH7
B1XDL1
A7FN83
B7N2P3
Q0TAG1
Q8FBE1
A4TRT2
Q31U87
A9QYS3
Q57HH1
P44777
Q8X6R8
B6I6K0
C0PXG5
B1X8V8
A6UPI8
Q8A1A0
A1AD97
B5RCB4
A8AL31
B7UNM3
Q6DA25
Q5PKG5
C4ZU87
B5FNS9
Q5LIN8
B1IU39
A8A705
Q1CEB1
Q0TFJ7
B7MZ98
Q5PEK9
P38715
Q56YU0
B7L9F8
P0AB87
B5F4S3
B4TUJ7
A6UQD0
Q838L1
C0Q3L1
Q88S52
B8DCW3
Q8ZJ03
B7NFK0
P25553
Q8FFN0
B5BCQ6
B4TPH2
Q8X6R5
A4FW36
Q83PE1
Q8Y3I8
Q57M64
Q8FEF0
Q58813
Q64ZS4
P11553
B5RDV4
B7LEY2
P0A9S1
C1CHF7
Q6LX65
P69737
A0AFI3
Q7MJI2
Q0TE57
Q0T157
Q97N97
Q8Z428
Q57KE0
Q8Z429
A7ZUB3
Q3YV74
A6UTG8
A4FWY9
B1LQZ6
B4TGN3
B4TBF6
B7NN63
B1LLJ9
A6L048
P0A9S2
Q8ZMC5
B5YZ39
Q66FF5
B5RFC6
C1CND0
A8A3T7
Q8X6R3
A9MSA6
A6UVT6
B7MG11
Q1R9H0
Q32DU2
Q6LY06
B7N736
A6TGA6
C1L0I0
Q71VR5
Q8ESW9
B4SYW1
P76469
B7MLC3
Q8XNL5
C1CU77
B8ZPZ6
A5UAS8
B5F0M6
B1IXU2
P0AB88
Q8ZMC6
Q8XE09
B1XB69
B1JND0
Q8ZNG0
A1AEY9
B5BF31
BRENDA Database
1.1.1.6
1.2.1.22
1.1.1.283
1.1.1.156
1.1.1.71
1.1.1.78
1.1.1.202
1.1.3.4
1.1.9.1
1.1.1.77
1.1.1.2
1.4.3.8
1.1.1.1
BRENDA Ligand Database
16600
104568
114588
Patent number
US2008032370
SureChEMBL Database
SCHEMBL289517
SABIO-RK Database
12492
554
9214
553
BKMS React Database
114588
104568
16600
Molecule Details
Wikipedia
Lactaldehyde
ChEBI
CHEBI:18419
A member of the class of propanals obtained by the reduction of the carboxylic group of lactic acid (2-hydroxypropanoic acid).
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
Chemspider ID
•
KEGG ID
•
Wikipedia Title
•
PubChem CID
•
CHEBI ID
•
CAS Number
•
PubChem SID
•
ACToR Database
•
UniProt Database
•
BRENDA Database
•
BRENDA Ligand Database
•
Patent number
•
SureChEMBL Database
•
SABIO-RK Database
•
BKMS React Database