NP-MRD: Showing NP-Card for istamycin c0 (NP0199997)

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Record Information

Version

2.0

Created at

2022-09-04 18:44:41 UTC

Updated at

2022-09-04 18:44:42 UTC

NP-MRD ID

NP0199997

Secondary Accession Numbers

None

Natural Product Identification

Common Name

istamycin c0

Description

Istamycin C0 belongs to the class of organic compounds known as aminocyclitol glycosides. These are organic compounds containing an amicocyclitol moiety glycosidically linked to a carbohydrate moiety. There are two major classes of aminoglycosides containing a 2-streptamine core. They are called 4,5- and 4,6-disubstituted 2-deoxystreptamines. istamycin c0 is found in Streptomyces tenjimariensis. Based on a literature review very few articles have been published on Istamycin C0.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 58 59  0  0  0  0  0  0  0  0999 V2000
    6.4147   -1.9352    0.6745 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1658   -0.6281   -0.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5022    0.3587    0.7692 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1407    0.1045    1.0985 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2256    0.1720   -0.1372 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5648    1.4412   -0.8373 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4207    2.3855   -0.9242 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1924    1.6041   -1.2886 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3181    0.9146   -2.5438 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8963    0.6173   -0.1510 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1775   -0.1387   -0.6293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3624    0.1604    0.0853 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7264   -1.1142    0.8040 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6976   -1.4614    1.7356 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0593   -0.8488    1.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0697   -0.7700    0.3652 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0384   -2.0167   -0.2651 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2184   -2.7168   -0.0644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8112    0.3328   -0.5927 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6323    1.4738   -0.2441 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0380    1.2658   -0.3354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3984    0.6897   -0.8372 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3109    2.1036   -0.7698 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9727   -0.0677    0.2618 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6046   -1.8479    1.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6226   -2.6683    0.4486 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3558   -2.3722    0.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6148   -0.8261   -0.9435 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1604   -0.2005   -0.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0606    0.8041    1.5019 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0639   -0.8975    1.5724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7980    0.8516    1.8426 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5875   -0.7119   -0.7625 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3985    2.0014   -0.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9814    1.2537   -1.8688 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6279    3.1020   -1.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2469    2.8950    0.0345 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3537    2.3320   -1.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6915    0.0825   -2.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2771    0.7227   -2.8492 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5648    1.2795    0.6925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0724    0.9231    0.8588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8933   -1.8866    0.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1301   -2.0491    2.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0556   -2.0299    1.3156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3018   -1.7486    2.0771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0185    0.0635    2.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0566   -0.6837    0.8601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1497   -3.7053   -0.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4168   -2.9038    1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1068   -2.1655   -0.4438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2397   -0.0152   -1.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3859    1.9003    0.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4166    1.7597   -1.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5279    1.7294    0.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3146    0.2106   -0.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0683    0.4610   -1.8890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2400    2.4136    0.1540 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  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 10 24  1  0
 24  5  1  0
 22 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  6
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  6
  9 39  1  0
  9 40  1  0
 10 41  1  1
 12 42  1  1
 13 43  1  6
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  1
 18 49  1  0
 18 50  1  0
 18 51  1  0
 19 52  1  6
 20 53  1  0
 21 54  1  0
 21 55  1  0
 21 56  1  0
 22 57  1  6
 23 58  1  0
M  END


  Mrv1652309042220442D          

 24 25  0  0  1  0            999 V2000
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  1  0  0  0
 10 24  1  0  0  0  0
  5 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0199997

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCNC[C@@H]1CC[C@@H](N)[C@@H](O[C@@H]2[C@@H](N)C[C@H](OC)[C@@H](NC)[C@H]2O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C16H34N4O4/c1-4-20-8-9-5-6-10(17)16(23-9)24-15-11(18)7-12(22-3)13(19-2)14(15)21/h9-16,19-21H,4-8,17-18H2,1-3H3/t9-,10+,11-,12-,13+,14+,15+,16+/m0/s1

> <INCHI_KEY>
MBIKACINXASGTE-PFCCBWJBSA-N

> <FORMULA>
C16H34N4O4

> <MOLECULAR_WEIGHT>
346.472

> <EXACT_MASS>
346.258005591

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
38.47932888463435

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3S,5S,6S)-3-amino-2-{[(2R,3R,6S)-3-amino-6-[(ethylamino)methyl]oxan-2-yl]oxy}-5-methoxy-6-(methylamino)cyclohexan-1-ol

> <JCHEM_LOGP>
-1.5869902636666664

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
4

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.475062619148488

> <JCHEM_PKA_STRONGEST_BASIC>
10.116445344082917

> <JCHEM_POLAR_SURFACE_AREA>
124.02000000000001

> <JCHEM_REFRACTIVITY>
90.35519999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3S,5S,6S)-3-amino-2-{[(2R,3R,6S)-3-amino-6-[(ethylamino)methyl]oxan-2-yl]oxy}-5-methoxy-6-(methylamino)cyclohexan-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -2.667  -0.000   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -1.334  -6.930   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       1.334  -2.310   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       6.668  -5.390   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   24                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   24                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   22                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   12   23                                                  
CONECT   23   22                                                            
CONECT   24   10    5                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₃₄N₄O₄

Average Mass

346.4720 Da

Monoisotopic Mass

346.25801 Da

IUPAC Name

(1R,2R,3S,5S,6S)-3-amino-2-{[(2R,3R,6S)-3-amino-6-[(ethylamino)methyl]oxan-2-yl]oxy}-5-methoxy-6-(methylamino)cyclohexan-1-ol

Traditional Name

(1R,2R,3S,5S,6S)-3-amino-2-{[(2R,3R,6S)-3-amino-6-[(ethylamino)methyl]oxan-2-yl]oxy}-5-methoxy-6-(methylamino)cyclohexan-1-ol

CAS Registry Number

Not Available

SMILES

CCNC[C@@H]1CC[C@@H](N)[C@@H](O[C@@H]2[C@@H](N)C[C@H](OC)[C@@H](NC)[C@H]2O)O1

InChI Identifier

InChI=1S/C16H34N4O4/c1-4-20-8-9-5-6-10(17)16(23-9)24-15-11(18)7-12(22-3)13(19-2)14(15)21/h9-16,19-21H,4-8,17-18H2,1-3H3/t9-,10+,11-,12-,13+,14+,15+,16+/m0/s1

InChI Key

MBIKACINXASGTE-PFCCBWJBSA-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
Streptomyces tenjimariensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aminocyclitol glycosides. These are organic compounds containing an amicocyclitol moiety glycosidically linked to a carbohydrate moiety. There are two major classes of aminoglycosides containing a 2-streptamine core. They are called 4,5- and 4,6-disubstituted 2-deoxystreptamines.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Aminocyclitol glycosides

Alternative Parents

Substituents

Amino cyclitol glycoside
Aminocyclitol or derivatives
Cyclohexanol
Cyclohexylamine
Cyclitol or derivatives
Oxane
Cyclic alcohol
1,2-aminoalcohol
Secondary alcohol
Ether
Secondary aliphatic amine
Dialkyl ether
Secondary amine
Organoheterocyclic compound
Oxacycle
Acetal
Organonitrogen compound
Primary aliphatic amine
Hydrocarbon derivative
Organopnictogen compound
Organic nitrogen compound
Amine
Alcohol
Primary amine
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

amino sugar (CHEBI:81445 )

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	-1.6	ChemAxon
pKa (Strongest Acidic)	13.48	ChemAxon
pKa (Strongest Basic)	10.12	ChemAxon
Physiological Charge	4	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	124.02 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	90.36 m³·mol⁻¹	ChemAxon
Polarizability	38.48 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

30791523

KEGG Compound ID

C17994

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13187055

PDB ID

Not Available

ChEBI ID

81445

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for istamycin c0 (NP0199997)

MOL for NP0199997 (istamycin c0)

3D MOL for NP0199997 (istamycin c0)

3D SDF for NP0199997 (istamycin c0)

3D-SDF for NP0199997 (istamycin c0)

PDB for NP0199997 (istamycin c0)

3D PDB for NP0199997 (istamycin c0)

SMILES for NP0199997 (istamycin c0)

INCHI for NP0199997 (istamycin c0)

Structure for NP0199997 (istamycin c0)

3D Structure for NP0199997 (istamycin c0)