NP-MRD: Showing NP-Card for Niazimicin (NP0136984)

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Record Information

Version

2.0

Created at

2022-05-30 16:38:07 UTC

Updated at

2022-05-30 16:38:07 UTC

NP-MRD ID

NP0136984

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Niazimicin

Description

Niazimicin belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Niazimicin is found in Moringa oleifera. Niazimicin is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 48  0  0  0  0  0  0  0  0999 V2000
   -7.7597    0.6797   -0.0678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9064   -0.4408    0.4816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1201   -0.0585    1.5708 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1605    0.9343    1.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6121    2.4758    1.8252 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7680    0.6693    1.2791 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4233   -0.6922    1.0404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9958   -0.9448    0.7495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0792    0.0007    0.3565 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2518   -0.2830    0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7328   -1.5555    0.2294 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0387   -1.8891   -0.0115 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9966   -0.9897   -0.4053 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5686   -1.3614   -1.6309 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2491   -0.2724   -2.1207 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3824    0.9263   -2.3796 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4248    0.0315   -1.2397 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3355   -1.0252   -1.3434 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0535    0.1543    0.2131 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5197    1.3989    0.5200 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1024   -0.9355    0.6607 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4693   -0.5595    1.8444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1733   -2.5504    0.6292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4802   -2.2377    0.8744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1264    1.5021   -0.4130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2542    0.2606   -0.9901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5399    0.9750    0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3359   -0.8600   -0.3688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5871   -1.2551    0.8219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1020    1.4701    1.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7759   -1.2839    1.9205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0085   -1.0724    0.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4541    1.0331    0.2442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8466    0.5656   -0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6948    0.0629   -0.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6720   -0.5773   -3.1216 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4614    1.6885   -1.5630 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6805    1.4435   -3.3246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3366    0.5753   -2.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9512    0.9424   -1.5383 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2561   -0.7172   -1.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9884    0.0158    0.8163 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3152    2.0060    0.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6006   -1.9183    0.7472 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7135   -1.1930    2.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2055   -3.5764    0.7355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1848   -3.0028    1.1837 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 11 23  1  0
 23 24  2  0
 24  8  1  0
 21 13  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
  9 33  1  0
 10 34  1  0
 13 35  1  6
 15 36  1  6
 16 37  1  0
 16 38  1  0
 16 39  1  0
 17 40  1  6
 18 41  1  0
 19 42  1  1
 20 43  1  0
 21 44  1  1
 22 45  1  0
 23 46  1  0
 24 47  1  0
M  END


  Mrv1652309272007452D          

 24 25  0  0  0  0            999 V2000
10015.132810016.0993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10017.990810017.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10018.706210017.3362    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10019.419510017.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10020.132710017.3362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10020.848010017.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10021.561310017.3362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10019.419510018.5730    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
10013.706710015.2747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10012.276410016.0993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10013.706710018.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10012.276410017.7484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10017.277010017.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10016.562610017.7492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10015.848010017.3367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10015.848010016.5118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10016.562410016.0992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10017.277010016.5118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10013.705310017.7492    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10012.990710017.3368    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10012.990710016.5117    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10013.705310016.0992    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10014.419810016.5117    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10014.419810017.3368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  8  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 13  1  0  0  0  0
  1 16  1  0  0  0  0
 13  2  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 24  1  0  0  0  0
 23 24  1  0  0  0  0
 23  1  1  1  0  0  0
 22  9  1  6  0  0  0
 21 10  1  6  0  0  0
 20 12  1  1  0  0  0
 19 11  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0136984

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCOC(=S)NCC1=CC=C(O[C@@H]2O[C@@H](C)[C@H](O)[C@@H](O)[C@H]2O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H23NO6S/c1-3-21-16(24)17-8-10-4-6-11(7-5-10)23-15-14(20)13(19)12(18)9(2)22-15/h4-7,9,12-15,18-20H,3,8H2,1-2H3,(H,17,24)/t9-,12-,13+,14+,15-/m0/s1

> <INCHI_KEY>
JOSHUAQJVMGTGS-NBUQLFNLSA-N

> <FORMULA>
C16H23NO6S

> <MOLECULAR_WEIGHT>
357.42

> <EXACT_MASS>
357.124608639

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.84090928431772

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[(4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)methyl]ethoxycarbothioamide

> <ALOGPS_LOGP>
1.05

> <JCHEM_LOGP>
1.2591060816666662

> <ALOGPS_LOGS>
-2.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.213742145714512

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.691851830189178

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6122003585840474

> <JCHEM_POLAR_SURFACE_AREA>
100.41000000000001

> <JCHEM_REFRACTIVITY>
90.91989999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.06e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[(4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)methyl]ethoxycarbothioamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-20         0                                  
HETATM    1  O   UNK     0    8694.9158696.719   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0    8700.2508699.797   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0    8701.5858699.027   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0    8702.9168699.797   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0    8704.2488699.027   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0    8705.5838699.797   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    8706.9158699.027   0.000  0.00  0.00           C+0
HETATM    8  S   UNK     0    8702.9168701.336   0.000  0.00  0.00           S+0
HETATM    9  O   UNK     0    8692.2528695.179   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0    8689.5838696.719   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0    8692.2528701.336   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0    8689.5838699.797   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0    8698.9178699.029   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8697.5848699.799   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8696.2508699.028   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8696.2508697.489   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8697.5838696.719   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8698.9178697.489   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8692.2508699.799   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8690.9168699.029   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8690.9168697.488   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8692.2508696.719   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0    8693.5848697.488   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0    8693.5848699.029   0.000  0.00  0.00           O+0
CONECT    1   16   23                                                       
CONECT    2    3   13                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    4                                                            
CONECT    9   22                                                            
CONECT   10   21                                                            
CONECT   11   19                                                            
CONECT   12   20                                                            
CONECT   13   14   18    2                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17    1                                                  
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
CONECT   19   20   24   11                                                  
CONECT   20   19   21   12                                                  
CONECT   21   20   22   10                                                  
CONECT   22   21   23    9                                                  
CONECT   23   22   24    1                                                  
CONECT   24   19   23                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
Niazimicine	HMDB
O-Ethyl 4-[(alpha-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
O-Ethyl 4-[(α-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
O-Ethyl-4-[(alpha-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
O-Ethyl-4-[(α-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
(e)-O-Ethyl 4-[(alpha-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
(e)-O-Ethyl 4-[(α-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
(e)-O-Ethyl-4-[(alpha-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
(e)-O-Ethyl-4-[(α-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
(Z)-O-Ethyl 4-[(alpha-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
(Z)-O-Ethyl 4-[(α-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
(Z)-O-Ethyl-4-[(alpha-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
(Z)-O-Ethyl-4-[(α-L-rhamnosyloxy)benzyl]thiocarbamate	HMDB
Niazimicin a	HMDB
Niazimicin b	HMDB
Niazimicine a	HMDB
Niazimicine b	HMDB
Niazimicin	HMDB

Chemical Formula

C₁₆H₂₃NO₆S

Average Mass

357.4200 Da

Monoisotopic Mass

357.12461 Da

IUPAC Name

N-[(4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)methyl]ethoxycarbothioamide

Traditional Name

N-[(4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)methyl]ethoxycarbothioamide

CAS Registry Number

Not Available

SMILES

CCOC(=S)NCC1=CC=C(O[C@@H]2O[C@@H](C)[C@H](O)[C@@H](O)[C@H]2O)C=C1

InChI Identifier

InChI=1S/C16H23NO6S/c1-3-21-16(24)17-8-10-4-6-11(7-5-10)23-15-14(20)13(19)12(18)9(2)22-15/h4-7,9,12-15,18-20H,3,8H2,1-2H3,(H,17,24)/t9-,12-,13+,14+,15-/m0/s1

InChI Key

JOSHUAQJVMGTGS-NBUQLFNLSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Moringa oleifera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Hexose monosaccharide
O-glycosyl compound
Phenoxy compound
Phenol ether
Monocyclic benzene moiety
Monosaccharide
Oxane
Benzenoid
Thiocarbamic acid ester
Thiocarbamic acid derivative
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Alcohol
Hydrocarbon derivative
Organopnictogen compound
Organonitrogen compound
Organosulfur compound
Organic nitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

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	1.05	ALOGPS
logP	1.26	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	8.69	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	100.41 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	90.92 m³·mol⁻¹	ChemAxon
Polarizability	36.84 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0031944

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB008634

KNApSAcK ID

Not Available

Chemspider ID

8423236

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10247749

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Niazimicin (NP0136984)

MOL for NP0136984 (Niazimicin)

3D MOL for NP0136984 (Niazimicin)

3D SDF for NP0136984 (Niazimicin)

3D-SDF for NP0136984 (Niazimicin)

PDB for NP0136984 (Niazimicin)

3D PDB for NP0136984 (Niazimicin)

SMILES for NP0136984 (Niazimicin)

INCHI for NP0136984 (Niazimicin)

Structure for NP0136984 (Niazimicin)

3D Structure for NP0136984 (Niazimicin)