NP-MRD: Showing NP-Card for 19-O-Acetylchaetoglobosin A (NP0050196)

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Record Information

Version

2.0

Created at

2022-04-27 20:30:32 UTC

Updated at

2022-04-27 20:30:32 UTC

NP-MRD ID

NP0050196

Secondary Accession Numbers

None

Natural Product Identification

Common Name

19-O-Acetylchaetoglobosin A

Description

19-O-Acetylchaetoglobosin A is found in Chaetomium globosum.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652304272222302D          

 42 47  0  0  1  0            999 V2000
    2.9949   -5.2944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8810   -4.4773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5317   -3.9701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2963   -4.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4101   -5.0972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7594   -5.6043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2505   -3.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4259   -3.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1976   -4.0151    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7126   -2.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3518   -1.7692    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5395   -1.6250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4257   -0.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6977   -0.4197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1676   -0.4471    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5970   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0390   -1.7396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8149   -1.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0003   -1.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3401   -0.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2982   -1.2024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0147    0.0652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0172    0.8896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4287    1.6047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1253    2.0466    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9475    2.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7070    1.7920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2297    1.1538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3959    0.3457    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1967    0.5443    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7691   -0.0498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5407   -0.8426    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7400   -1.0412    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1131   -1.4367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9974    0.7430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5618   -0.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8629    2.8288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7755    1.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8228   -0.1011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3708    0.5156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1789    0.3494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1107    1.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  3  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  7 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15 13  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 29 28  1  1  0  0  0
 15 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 11  1  1  0  0  0
 15 33  1  0  0  0  0
 32 34  1  1  0  0  0
 31 35  1  0  0  0  0
 30 35  1  6  0  0  0
 31 36  1  1  0  0  0
 25 37  1  1  0  0  0
 23 38  1  0  0  0  0
 22 39  1  6  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
M  END


  Mrv1652304272222302D          

 42 47  0  0  1  0            999 V2000
    2.9949   -5.2944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8810   -4.4773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5317   -3.9701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2963   -4.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4101   -5.0972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7594   -5.6043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2505   -3.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4259   -3.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1976   -4.0151    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7126   -2.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3518   -1.7692    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5395   -1.6250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4257   -0.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6977   -0.4197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1676   -0.4471    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5970   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0390   -1.7396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8149   -1.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0003   -1.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3401   -0.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2982   -1.2024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0147    0.0652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0172    0.8896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4287    1.6047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1253    2.0466    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9475    2.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7070    1.7920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2297    1.1538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3959    0.3457    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1967    0.5443    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7691   -0.0498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5407   -0.8426    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7400   -1.0412    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1131   -1.4367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9974    0.7430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5618   -0.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8629    2.8288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7755    1.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8228   -0.1011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3708    0.5156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1789    0.3494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1107    1.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  3  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  7 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15 13  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 29 28  1  1  0  0  0
 15 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 11  1  1  0  0  0
 15 33  1  0  0  0  0
 32 34  1  1  0  0  0
 31 35  1  0  0  0  0
 30 35  1  6  0  0  0
 31 36  1  1  0  0  0
 25 37  1  1  0  0  0
 23 38  1  0  0  0  0
 22 39  1  6  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0050196

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]2[C@H](CC3=CNC4=CC=CC=C34)NC(=O)[C@]22[C@@H](\C=C/C[C@H](C)\C=C(C)/[C@@H](OC(C)=O)C(=O)\C=C/C2=O)[C@@H]2O[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C34H38N2O6/c1-18-9-8-11-24-31-33(5,42-31)20(3)29-26(16-22-17-35-25-12-7-6-10-23(22)25)36-32(40)34(24,29)28(39)14-13-27(38)30(19(2)15-18)41-21(4)37/h6-8,10-15,17-18,20,24,26,29-31,35H,9,16H2,1-5H3,(H,36,40)/b11-8-,14-13-,19-15-/t18-,20-,24-,26-,29-,30+,31-,33+,34-/m0/s1

> <INCHI_KEY>
AZLAYOMQTNEYFJ-DZTIUTMXSA-N

> <FORMULA>
C34H38N2O6

> <MOLECULAR_WEIGHT>
570.686

> <EXACT_MASS>
570.272986952

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
62.03378246363176

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3E,6R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-19-[(1H-indol-3-yl)methyl]-7,9,16,17-tetramethyl-2,5,21-trioxo-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11-trien-6-yl acetate

> <ALOGPS_LOGP>
4.08

> <JCHEM_LOGP>
4.773006316333332

> <ALOGPS_LOGS>
-5.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.28911049081314

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.68611597105265

> <JCHEM_PKA_STRONGEST_BASIC>
-2.56009003081008

> <JCHEM_POLAR_SURFACE_AREA>
117.86000000000001

> <JCHEM_REFRACTIVITY>
159.99630000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.28e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3E,6R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-19-(1H-indol-3-ylmethyl)-7,9,16,17-tetramethyl-2,5,21-trioxo-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11-trien-6-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-APR-22         0                                  
HETATM    1  C   UNK     0       5.590  -9.883   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.378  -8.358   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.593  -7.411   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.020  -7.989   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.232  -9.515   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.018 -10.461   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.068  -5.963   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.528  -6.015   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       4.102  -7.495   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       6.930  -4.687   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.257  -3.302   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       4.740  -3.033   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       4.528  -1.508   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.169  -0.783   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.913  -0.835   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.848  -1.947   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.673  -3.247   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.388  -2.437   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.867  -2.192   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.635  -1.269   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.557  -2.244   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.027   0.122   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.032   1.661   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.800   2.995   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.101   3.820   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.635   3.947   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.053   3.345   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.029   2.154   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.339   0.645   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.834   1.016   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.902  -0.093   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.476  -1.573   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.981  -1.944   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.545  -2.682   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       9.328   1.387   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      10.382  -0.519   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.611   5.280   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -1.448   2.087   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -1.536  -0.189   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -2.559   0.963   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -4.067   0.652   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -2.073   2.424   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3    9                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    3    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8    2                                                       
CONECT   10    7   11                                                       
CONECT   11   10   12   33                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   29   33                                             
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   39                                                  
CONECT   23   22   24   38                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   37                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   15   30                                                  
CONECT   30   29   31   35                                                  
CONECT   31   30   32   35   36                                             
CONECT   32   31   33   34                                                  
CONECT   33   32   11   15                                                  
CONECT   34   32                                                            
CONECT   35   31   30                                                       
CONECT   36   31                                                            
CONECT   37   25                                                            
CONECT   38   23                                                            
CONECT   39   22   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₃₈N₂O₆

Average Mass

570.6860 Da

Monoisotopic Mass

570.27299 Da

IUPAC Name

(1S,3E,6R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-19-[(1H-indol-3-yl)methyl]-7,9,16,17-tetramethyl-2,5,21-trioxo-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11-trien-6-yl acetate

Traditional Name

(1S,3E,6R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-19-(1H-indol-3-ylmethyl)-7,9,16,17-tetramethyl-2,5,21-trioxo-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11-trien-6-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]2[C@H](CC3=CNC4=CC=CC=C34)NC(=O)[C@]22[C@@H](\C=C/C[C@H](C)\C=C(C)/[C@@H](OC(C)=O)C(=O)\C=C/C2=O)[C@@H]2O[C@]12C

InChI Identifier

InChI=1S/C34H38N2O6/c1-18-9-8-11-24-31-33(5,42-31)20(3)29-26(16-22-17-35-25-12-7-6-10-23(22)25)36-32(40)34(24,29)28(39)14-13-27(38)30(19(2)15-18)41-21(4)37/h6-8,10-15,17-18,20,24,26,29-31,35H,9,16H2,1-5H3,(H,36,40)/b11-8-,14-13-,19-15-/t18-,20-,24-,26-,29-,30+,31-,33+,34-/m0/s1

InChI Key

AZLAYOMQTNEYFJ-DZTIUTMXSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Chaetomium globosum	Fungi	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	4.08	ALOGPS
logP	4.77	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	13.69	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	117.86 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	160 m³·mol⁻¹	ChemAxon
Polarizability	62.03 Å³	ChemAxon
Number of Rings	6	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

Not Available

References

General References

Not Available

Showing NP-Card for 19-O-Acetylchaetoglobosin A (NP0050196)

MOL for NP0050196 (19-O-Acetylchaetoglobosin A)

3D MOL for NP0050196 (19-O-Acetylchaetoglobosin A)

3D SDF for NP0050196 (19-O-Acetylchaetoglobosin A)

3D-SDF for NP0050196 (19-O-Acetylchaetoglobosin A)

PDB for NP0050196 (19-O-Acetylchaetoglobosin A)

3D PDB for NP0050196 (19-O-Acetylchaetoglobosin A)

SMILES for NP0050196 (19-O-Acetylchaetoglobosin A)

INCHI for NP0050196 (19-O-Acetylchaetoglobosin A)

Structure for NP0050196 (19-O-Acetylchaetoglobosin A)

3D Structure for NP0050196 (19-O-Acetylchaetoglobosin A)