NP-MRD: Showing NP-Card for N-Acetyl-9-O-acetylneuraminic acid (NP0086648)

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Record Information

Version

2.0

Created at

2022-05-11 16:27:04 UTC

Updated at

2022-05-11 16:27:04 UTC

NP-MRD ID

NP0086648

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N-Acetyl-9-O-acetylneuraminic acid

Description

N-Acetyl-9-O-acetylneuraminic acid, also known as 9-O-acetylsialic acid or 9-anana, belongs to the class of organic compounds known as neuraminic acids. These are carbohydrate derivatives containing a neuraminic acid moiety. N-Acetyl-9-O-acetylneuraminic acid was first documented in 1976 (PMID: 1017796). N-Acetyl-9-O-acetylneuraminic acid is an extremely weak basic (essentially neutral) compound (based on its pKa) (PMID: 3623000) (PMID: 3700379).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 45  0  0  0  0  0  0  0  0999 V2000
   -0.9084   -3.5345   -1.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1316   -2.3930   -0.7337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4418   -2.6521    0.4551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0111   -1.0393   -1.1345 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2243    0.0563   -0.2550 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5161    0.7570   -0.7189 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5665   -0.1237   -0.8123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8276    1.8466    0.3080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6356    2.7849    0.2959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4829    3.2280   -1.0106 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8527    3.9118    1.2382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8757    5.0757    0.7917 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0283    3.6879    2.5926 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5302    2.0485    0.7350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1816    1.1023   -0.2560 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2207    0.6840   -0.0551 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5961   -0.2513   -1.0181 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5759    0.1564    1.2949 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2379    1.0232    2.3317 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0738   -0.0387    1.3921 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4964   -0.8940    0.3816 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1295   -2.2023    0.1843 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7158   -2.9347   -0.9865 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3286   -2.7373    0.9750 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8684   -3.2515   -2.7081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6578   -4.3397   -1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0846   -3.9909   -1.4034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537   -0.8729   -2.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4958   -0.3042    0.7807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2672    1.2687   -1.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9176   -0.3345    0.0830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7627    2.3378    0.0083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8644    1.3600    1.2848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3799    3.4304   -1.3900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4063    2.9845    3.0081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2453    1.6622   -1.2138 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8662    1.5792   -0.2422 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3101    0.0451   -1.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1249   -0.8449    1.4288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6067    0.5553    2.9150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3459   -0.4961    2.3910 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6033    0.9352    1.3956 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5642   -4.0216   -0.8392 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1823   -2.6159   -1.8894 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7703   -2.6475   -1.0508 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  6
  9 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
  9 11  1  0
 11 13  1  0
 11 12  2  0
 15  5  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  5 29  1  1
  6 30  1  6
  7 31  1  0
  8 32  1  0
  8 33  1  0
 10 34  1  0
 15 36  1  6
 16 37  1  6
 17 38  1  0
 18 39  1  1
 19 40  1  0
 20 41  1  0
 20 42  1  0
 23 43  1  0
 23 44  1  0
 23 45  1  0
 13 35  1  0
M  END

N-Acetyl-9-O-acetylneuraminic acid.mol
  Mrv1652305231920212D          

 24 24  0  0  0  0            999 V2000
    0.9966    1.9279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.1526    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5269    1.0094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.3276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -0.9099    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -1.3224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.3224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -2.1474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.3224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.3276    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0849    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.1526    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    1.5651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.5651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4663    2.5599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8091    2.0711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.5599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.5599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.1526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  6  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
  2 16  1  0  0  0  0
  1 17  2  0  0  0  0
  1 18  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 11 19  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 13 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086648

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)N[C@@H]1[C@@H](O)C[C@](O)(O[C@H]1[C@H](O)[C@H](O)COC(C)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H21NO10/c1-5(15)14-9-7(17)3-13(22,12(20)21)24-11(9)10(19)8(18)4-23-6(2)16/h7-11,17-19,22H,3-4H2,1-2H3,(H,14,15)(H,20,21)/t7-,8+,9+,10+,11+,13-/m0/s1

> <INCHI_KEY>
NYWZBRWKDRMPAS-GRRZBWEESA-N

> <FORMULA>
C13H21NO10

> <MOLECULAR_WEIGHT>
351.3065

> <EXACT_MASS>
351.116545897

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
31.82084761600297

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,4S,5R,6R)-6-[(1R,2R)-3-(acetyloxy)-1,2-dihydroxypropyl]-5-acetamido-2,4-dihydroxyoxane-2-carboxylic acid

> <ALOGPS_LOGP>
-2.35

> <JCHEM_LOGP>
-3.122812108666666

> <ALOGPS_LOGS>
-0.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.106531603733684

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8360819006184834

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3427502330402574

> <JCHEM_POLAR_SURFACE_AREA>
182.85

> <JCHEM_REFRACTIVITY>
72.93289999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.03e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-O-acetylsialic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-MAY-19   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: N-Acetyl-9-O-acetylneuraminic acid.mol            
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-MAY-19         0                                  
HETATM    1  C   UNK     0       1.860   3.599   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334   2.152   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.850   1.884   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.334   0.612   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.000  -0.158   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -1.698   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.334  -2.468   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334  -2.468   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.334  -4.008   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667  -1.698   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.001  -2.468   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.334   0.612   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -2.667  -0.158   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -1.334   2.152   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.667   2.922   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.000   2.922   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.870   4.778   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       3.377   3.866   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.001  -4.008   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.335  -4.778   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.667  -4.778   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.001   0.612   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -4.001   2.152   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -5.335  -0.158   0.000  0.00  0.00           C+0
CONECT    1    2   17   18                                                  
CONECT    2    1    3    4   16                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   19                                                       
CONECT   12    5   13   14                                                  
CONECT   13   12   22                                                       
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    2                                                       
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19   20   21   11                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   23   24   13                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Value	Source
9-Anana	ChEBI
9-O-Acetyl-N-acetylneuraminic acid	ChEBI
9-O-Acetylsialic acid	ChEBI
9-O-Acetyl-N-acetylneuraminate	Generator
9-O-Acetylsialate	Generator
N-Acetyl-9-O-acetylneuraminate	Generator
N,9-O-Diacetylneuraminate	HMDB
N,9-O-Diacetylneuraminic acid	HMDB
Neu5,9ac2	HMDB

Chemical Formula

C₁₃H₂₁NO₁₀

Average Mass

351.3065 Da

Monoisotopic Mass

351.11655 Da

IUPAC Name

(2S,4S,5R,6R)-6-[(1R,2R)-3-(acetyloxy)-1,2-dihydroxypropyl]-5-acetamido-2,4-dihydroxyoxane-2-carboxylic acid

Traditional Name

9-O-acetylsialic acid

CAS Registry Number

Not Available

SMILES

CC(=O)N[C@@H]1[C@@H](O)C[C@](O)(O[C@H]1[C@H](O)[C@H](O)COC(C)=O)C(O)=O

InChI Identifier

InChI=1S/C13H21NO10/c1-5(15)14-9-7(17)3-13(22,12(20)21)24-11(9)10(19)8(18)4-23-6(2)16/h7-11,17-19,22H,3-4H2,1-2H3,(H,14,15)(H,20,21)/t7-,8+,9+,10+,11+,13-/m0/s1

InChI Key

NYWZBRWKDRMPAS-GRRZBWEESA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
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Ovis aries	FooDB	FooDB
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Chemical Taxonomy

Description

Belongs to the class of organic compounds known as neuraminic acids. These are carbohydrate derivatives containing a neuraminic acid moiety.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Neuraminic acids

Alternative Parents

Substituents

Neuraminic acid
C-glucuronide
C-glycosyl compound
Glycosyl compound
Alpha-hydroxy acid
Dicarboxylic acid or derivatives
Hydroxy acid
Pyran
Oxane
Carboxylic acid ester
Hemiacetal
Secondary alcohol
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxide
Carbonyl group
Alcohol
Organonitrogen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

N-acetyl-O-acetylneuraminic acid (CHEBI:21500 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-2.4	ALOGPS
logP	-3.1	ChemAxon
logS	-0.53	ALOGPS
pKa (Strongest Acidic)	2.84	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	182.85 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	72.93 m³·mol⁻¹	ChemAxon
Polarizability	31.82 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0000794

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB022249

KNApSAcK ID

Not Available

Chemspider ID

110484

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

5759

PubChem Compound

123962

PDB ID

Not Available

ChEBI ID

21500

Good Scents ID

Not Available

References

General References

Haverkamp J, Schauer R, Wember M: Neuraminic acid derivatives newly discovered in humans: N-acetyl-9-O-L-lactoylneuraminic acid, N,9-O-Diacetylneuraminic acid and N-acetyl-2,3-dehydro-2-deoxyneuraminic acid. Hoppe Seylers Z Physiol Chem. 1976 Dec;357(12):1699-705. doi: 10.1515/bchm2.1976.357.2.1699. [PubMed:1017796 ]
Muchmore EA, Varki NM, Fukuda M, Varki A: Developmental regulation of sialic acid modifications in rat and human colon. FASEB J. 1987 Sep;1(3):229-35. doi: 10.1096/fasebj.1.3.3623000. [PubMed:3623000 ]
Rogers GN, Herrler G, Paulson JC, Klenk HD: Influenza C virus uses 9-O-acetyl-N-acetylneuraminic acid as a high affinity receptor determinant for attachment to cells. J Biol Chem. 1986 May 5;261(13):5947-51. [PubMed:3700379 ]

Showing NP-Card for N-Acetyl-9-O-acetylneuraminic acid (NP0086648)

MOL for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)

3D MOL for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)

3D SDF for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)

3D-SDF for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)

PDB for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)

3D PDB for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)

SMILES for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)

INCHI for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)

Structure for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)

3D Structure for NP0086648 (N-Acetyl-9-O-acetylneuraminic acid)