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Molecule
ID:127511
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₁₃NO₅
Molecular Mass
179.17112
Exact Mass
179.07937252
Charge
0
InChI
InChI=1S/C6H13NO5/c7-3-5(10)4(9)2(1-8)12-6(3)11/h2-6,8-11H,1,7H2/t2-,3-,4+,5-,6?/m1/s1
InChIKey
MSWZFWKMSRAUBD-GASJEMHNSA-N
Canonic Smiles
OC[C@H]1OC(O)[C@@H]([C@H]([C@H]1O)O)N
Isomeric Smiles
O[C@H]1[C@@H](O)[C@H](OC(O)[C@@H]1N)CO
Calculated Properties
JChem
LogD (pH = 7.4)
-3.80
LogD (pH = 5.5)
-5.49
Log P
-3.04
Rotatable Bonds
1
H Donor
5
H Acceptors
6
Lipinski's Rule of Five
true
Acid pKa
8.08
Polar Surface Area
116.17
Polarizability
16.74
Molar Refractivity
37.58
LOG S
0.25
Data Source
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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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Bioactivity
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Galactosamine
PubChem
24154
ChEBI
CHEBI:60312
Names and Identifiers
IUPAC Traditional name
galactosamine
Synonyms
α-D-galactosamine
Galactosamine
D-Galactosamine
Galactosamine
Chondrosamine
D-GalN
D-2-Amino-2-deoxygalactose
2-Amino-2-deoxy-D-galactose
D-Chondrosamine
2-amino-2-deoxy-D-galactopyranose
IUPAC name
(3R,4R,5R,6R)-3-amino-6-(hydroxymethyl)oxane-2,4,5-triol
Registration numbers
Chemspider ID
22576
PubChem CID
24154
CAS Number
7535-00-4
CHEMBL
207280
CHEMBL3304228
CHEBI ID
60312
CHEBI:60312
Wikipedia Title
Galactosamine
PubChem SID
162221830
99365005
UniProt Database
Q8TDX6
Q6P9A2
Q10471
Q9Y117
Q8CF93
Q6L9W6
Q6WV17
Q6WV20
P34059
Q6UE39
Q8BG28
Q9R0C5
Q9JJ05
Q8E372
Q8C102
Q09199
Q8IZ52
O45947
Q9JJ06
Q5DTK1
P0ACK3
Q9VUT6
P0AF18
P36231
P34678
Q05097
Q36736
Q8IA41
Q5XIG6
Q86SF2
P16030
P56625
Q8NCR0
Q14435
Q5RAL7
Q10473
Q9NS00
Q8N3T1
Q86SR1
Q6L8S8
Q5RFJ6
Q9DBH5
P19035
P0C8K1
Q68FH4
Q940S3
P42912
Q6WV19
Q96FL9
O88178
O32274
Q9Z0F0
Q16222
Q9NY28
Q8BJQ9
Q8C7U7
Q7SYI5
Q91YN5
A8Y236
Q00973
Q07537
Q7Z7M9
Q864U6
Q9D2N8
Q8N4A0
Q0VC84
Q7K755
Q8K1B9
Q18515
Q5F3G7
Q9CMP0
O08912
P0C6E3
Q0P9C9
P84870
O75752
Q8N428
Q96L58
Q70JA7
Q9JJ61
Q01415
Q6DJR8
Q8MVS5
Q920V1
Q6P6V1
Q6P9S7
Q8NCW6
Q8VI38
Q6WV16
P15848
Q8L0V4
P70419
P33727
Q2MGH6
O00834
Q9KIP8
Q921L8
Q9ET32
Q8NCH0
Q6GNL1
Q8MYY6
P49256
P50429
O64765
P83422
Q6IQX7
Q29121
Q925R7
Q766D5
Q10472
P42906
P83424
A9KQ75
B3EWR5
P0ACK4
Q8X7P7
Q95158
Q5TJE8
O61397
Q08BL3
Q12907
Q8DR60
Q7TT15
Q8DR77
Q6AY39
Q32KH5
P46918
P16442
P17900
Q8NCL4
Q8BGT9
O35744
P42907
Q09200
Q9HCQ5
Q32KJ6
Q8MRC9
Q8IXK2
Q80V53
Q95ZJ1
P16351
Q793U7
Q8BVG5
P36230
O88422
Q8MV48
O96024
Q8C1F4
Q10468
Q8N6G5
Q76KP1
Q8IA42
P46917
P58591
Q0P9C5
Q502B3
Q6ZQ11
Q41159
P86702
Q0P9C7
Q8HXX6
Q8IA44
Q8IA43
P86922
Q5M900
Q5EA41
Q60648
O61394
Q9A0T3
B3FN88
Q6NRQ1
P0A6T3
O08832
Q9GM01
Q49A17
P38649
Q6IS24
P0C8K0
Q8IUC8
Q6PB93
Q8I136
Q8WNQ7
Q86X52
A9KIW5
P98092
Q5R6J8
Q8CFC4
Q80VA0
P45895
Q9U2C4
A9WNA0
Q45410
P50430
P0AB74
P0ACK2
Q7K237
Q91Z92
Q571E4
ACToR Database
90-76-6
7535-00-4
BKMS React Database
233868
210442
22053
51277
3997
27112
6525
BRENDA Database
1.1.1.121
2.7.7.9
1.1.3.9
2.7.1.162
3.2.1.52
3.1.6.4
3.2.1.109
2.7.1.6
1.1.3.29
3.2.1.23
4.1.1.40
2.4.1.5
3.5.1.33
1.4.3.21
2.4.1.37
3.2.1.14
7.5.2.11
2.3.1.3
BRENDA Ligand Database
3997
27112
233868
6525
22053
210442
51277
Reaxys Registry
2042269
KEGG ID
C02262
CompTox Database
DTXSID7043871
PubMed Citation Links
28821814
28752362
19913595
28709622
28921968
17456244
MetaboLights Database
MTBLS533
MTBLS442
MTBLS301
MTBLS1861
MTBLS353
MTBLS697
Beilstein Number
2042269
SureChEMBL Database
SCHEMBL28731
SABIO-RK Database
11479
Properties
Physical Property
Melting Point
180 °C (HCl salt)
Source
Molecule Details
Wikipedia
Galactosamine
ChEBI
CHEBI:60312
The pyranose form of D-galactosamine.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
Chemspider ID
•
PubChem CID
•
CAS Number
•
CHEMBL
•
CHEBI ID
•
Wikipedia Title
•
PubChem SID
•
UniProt Database
•
ACToR Database
•
BKMS React Database
•
BRENDA Database
•
BRENDA Ligand Database
•
Reaxys Registry
•
KEGG ID
•
CompTox Database
•
PubMed Citation Links
•
MetaboLights Database
•
Beilstein Number
•
SureChEMBL Database
•
SABIO-RK Database