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Molecule
ID:1431
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₁₃O₁₀P
Molecular Mass
276.135181
Exact Mass
276.02463325
Charge
0
InChI
InChI=1S/C6H13O10P/c7-2(1-16-17(13,14)15)3(8)4(9)5(10)6(11)12/h2-5,7-10H,1H2,(H,11,12)(H2,13,14,15)/t2-,3+,4-,5-/m0/s1
InChIKey
BIRSGZKFKXLSJQ-QTBDOELSSA-N
Canonic Smiles
O[C@H]([C@H]([C@@H]([C@@H](C(=O)O)O)O)O)COP(=O)(O)O
Isomeric Smiles
O[C@@H](COP(=O)(O)O)[C@@H](O)[C@H](O)[C@H](O)C(=O)O
Calculated Properties
JChem
LogD (pH = 7.4)
-9.61
LogD (pH = 5.5)
-7.03
Log P
-3.53
Rotatable Bonds
7
H Donor
7
H Acceptors
9
Lipinski's Rule of Five
false
Acid pKa
1.49
Polar Surface Area
184.98
Polarizability
21.80
Molar Refractivity
49.14
LOG S
1.51
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Properties
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Molecular Spectra
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General Information
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Data Source
Academic Data
PubChem
446821
DrugBank
DB01655
ChEBI
CHEBI:43824
Names and Identifiers
IUPAC Traditional name
@L-guluronic acid 6-phosphate
L-guluronic acid 6-phosphate
Synonyms
L-Guluronic Acid 6-Phosphate
L-gulonic acid 6-phosphate
6-O-phosphono-L-gulonic acid
IUPAC name
(2S,3S,4R,5S)-2,3,4,5-tetrahydroxy-6-(phosphonooxy)hexanoic acid
Registration numbers
PubChem CID
446821
PubChem SID
46508101
160964890
223442564
PDBeChem Database
LG6
Protein Data Bank
1kw1
1q6o
BRENDA Ligand Database
125196
BRENDA Database
4.1.1.85
CHEBI ID
CHEBI:43824
BKMS React Database
125196
Related Proteins
PDB Bank
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1KW1
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1Q6O
Molecule Details
DrugBank
DB01655
Drug information: experimental
ChEBI
CHEBI:43824
A gulonic acid derivative that is L-gulonic acid carrying a phosphate group at position 6.
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Bioactivity
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PubChem CID
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PubChem SID
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PDBeChem Database
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Protein Data Bank
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BRENDA Ligand Database
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BRENDA Database
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CHEBI ID
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BKMS React Database