NP-MRD: Showing NP-Card for Antiostatin A4 (NP0061595)

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Record Information

Version

2.0

Created at

2022-04-28 06:21:32 UTC

Updated at

2022-04-28 06:21:32 UTC

NP-MRD ID

NP0061595

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Antiostatin A4

Description

N-(1-heptyl-3-hydroxy-2-methyl-9H-carbazol-4-yl)ethanimidic acid belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. Antiostatin A4 is found in Streptomyces cyaneus 2007-SV1. N-(1-heptyl-3-hydroxy-2-methyl-9H-carbazol-4-yl)ethanimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231522372D          

 26 28  0  0  0  0            999 V2000
    4.0444   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7589   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4733   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1878   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9023   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6167   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3312   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0457   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7601   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7601   -0.1582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4746   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1891   -0.9832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4746   -2.2207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1891   -2.6332    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.1891   -3.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9036   -3.8707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4746   -3.8707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7601   -2.6332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5886   -3.4402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0735   -4.1076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7380   -4.8613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9175   -4.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4326   -4.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7681   -3.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4326   -2.7727    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.0457   -2.2207    0.0000 C   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
  4  5  1  0  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  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 19 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  8 26  1  0  0  0  0
 18 26  2  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
    6.2100    1.0687    1.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7270    1.3416    1.2506 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9866    1.1011   -0.0489 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1701   -0.3224   -0.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4961   -0.7100   -1.7362 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9991   -0.5309   -1.7237 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3446   -1.3439   -0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1199   -1.2355   -0.5869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9198   -1.9921   -1.4100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4110   -3.0194   -2.3557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3127   -1.8123   -1.3244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1115   -2.5792   -2.1596 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8368   -0.9031   -0.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2434   -0.7495   -0.3836 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9591    0.1516   -1.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4327    0.2547   -1.0874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3307    0.8599   -2.0256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0212   -0.1555    0.3812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6554   -0.3092    0.3189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0877    0.5254    1.2099 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0185    1.2361    1.8715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9647    2.2022    2.8636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1161    2.7678    3.3645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3218    2.3452    2.8506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3805    1.3791    1.8578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2312    0.8093    1.3520 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4384   -0.0147    1.0667 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6042    1.5002    0.1503 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7831    1.5146    1.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6183    2.4165    1.4974 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3261    0.7229    2.0671 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3694    1.8023   -0.7933 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9205    1.3559    0.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2677   -0.4829   -0.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583   -0.9931    0.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6720   -1.8150   -1.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9553   -0.2215   -2.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7680    0.5730   -1.6063 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6108   -0.7980   -2.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5971   -2.4294   -0.8328 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8289   -1.1189    0.3328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2411   -3.2267   -3.0923 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4709   -2.7534   -2.9165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2561   -3.9986   -1.8436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1126   -2.4462   -2.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7514   -1.3506    0.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7183    0.8388   -0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8603   -0.7574   -0.9383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8869    0.8064   -1.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9323    0.6238    1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0143    2.5328    3.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0804    3.5365    4.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2363    2.7672    3.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3224    1.0359    1.4477 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  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 13 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 26  2  0
 26 25  1  0
 25 24  2  0
 24 23  1  0
 23 22  2  0
 19  8  1  0
 22 21  1  0
 26 18  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
 10 42  1  0
 10 43  1  0
 10 44  1  0
 12 45  1  0
 14 46  1  0
 16 47  1  0
 16 48  1  0
 16 49  1  0
 20 50  1  0
 25 54  1  0
 24 53  1  0
 23 52  1  0
 22 51  1  0
M  END


  Mrv1533004231522372D          

 26 28  0  0  0  0            999 V2000
    4.0444   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7589   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4733   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1878   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9023   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6167   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3312   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0457   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7601   -0.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7601   -0.1582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4746   -1.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1891   -0.9832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4746   -2.2207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1891   -2.6332    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.1891   -3.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9036   -3.8707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4746   -3.8707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7601   -2.6332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5886   -3.4402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0735   -4.1076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7380   -4.8613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9175   -4.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4326   -4.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7681   -3.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4326   -2.7727    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.0457   -2.2207    0.0000 C   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
  4  5  1  0  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  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 19 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  8 26  1  0  0  0  0
 18 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0061595

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC1=C(C)C(O)=C(NC(C)=O)C2=C1NC1=C2C=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H28N2O2/c1-4-5-6-7-8-11-16-14(2)22(26)21(23-15(3)25)19-17-12-9-10-13-18(17)24-20(16)19/h9-10,12-13,24,26H,4-8,11H2,1-3H3,(H,23,25)

> <INCHI_KEY>
UDYDNCMLIJAFMJ-UHFFFAOYSA-N

> <FORMULA>
C22H28N2O2

> <MOLECULAR_WEIGHT>
352.478

> <EXACT_MASS>
352.21507815

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.32692201671365

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-(1-heptyl-3-hydroxy-2-methyl-9H-carbazol-4-yl)acetamide

> <ALOGPS_LOGP>
5.44

> <JCHEM_LOGP>
5.719285503666667

> <ALOGPS_LOGS>
-5.44

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.482951523528271

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.314494512319266

> <JCHEM_PKA_STRONGEST_BASIC>
-4.556928806102304

> <JCHEM_POLAR_SURFACE_AREA>
65.12

> <JCHEM_REFRACTIVITY>
108.00450000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.29e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-(1-heptyl-3-hydroxy-2-methyl-9H-carbazol-4-yl)acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       7.550  -1.835   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.883  -2.605   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.217  -1.835   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.551  -2.605   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.884  -1.835   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.218  -2.605   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      15.552  -1.835   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.885  -2.605   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.219  -1.835   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.219  -0.295   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      19.553  -2.605   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      20.886  -1.835   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      19.553  -4.145   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      20.886  -4.915   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      20.886  -6.455   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      22.220  -7.225   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      19.553  -7.225   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.219  -4.915   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.899  -6.422   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      18.804  -7.668   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.178  -9.074   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      16.646  -9.235   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      15.741  -7.990   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      16.367  -6.583   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      15.741  -5.176   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      16.885  -4.145   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   26                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   13   19   26                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25    8   18                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
N-(1-Heptyl-3-hydroxy-2-methyl-9H-carbazol-4-yl)ethanimidate	Generator

Chemical Formula

C₂₂H₂₈N₂O₂

Average Mass

352.4780 Da

Monoisotopic Mass

352.21508 Da

IUPAC Name

N-(1-heptyl-3-hydroxy-2-methyl-9H-carbazol-4-yl)acetamide

Traditional Name

N-(1-heptyl-3-hydroxy-2-methyl-9H-carbazol-4-yl)acetamide

CAS Registry Number

Not Available

SMILES

CCCCCCCC1=C(C)C(O)=C(NC(C)=O)C2=C1NC1=C2C=CC=C1

InChI Identifier

InChI=1S/C22H28N2O2/c1-4-5-6-7-8-11-16-14(2)22(26)21(23-15(3)25)19-17-12-9-10-13-18(17)24-20(16)19/h9-10,12-13,24,26H,4-8,11H2,1-3H3,(H,23,25)

InChI Key

UDYDNCMLIJAFMJ-UHFFFAOYSA-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
Streptomyces cyaneus 2007-SV1	Bacteria	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
Hydroxyindole
Indole
N-acetylarylamine
N-arylamide
Phenol
Benzenoid
Acetamide
Pyrrole
Heteroaromatic compound
Secondary carboxylic acid amide
Carboxamide group
Azacycle
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	5.44	ALOGPS
logP	5.72	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	8.31	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	65.12 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	108 m³·mol⁻¹	ChemAxon
Polarizability	42.33 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14805051

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Antiostatin A4 (NP0061595)

MOL for NP0061595 (Antiostatin A4)

3D MOL for NP0061595 (Antiostatin A4)

3D SDF for NP0061595 (Antiostatin A4)

3D-SDF for NP0061595 (Antiostatin A4)

PDB for NP0061595 (Antiostatin A4)

3D PDB for NP0061595 (Antiostatin A4)

SMILES for NP0061595 (Antiostatin A4)

INCHI for NP0061595 (Antiostatin A4)

Structure for NP0061595 (Antiostatin A4)

3D Structure for NP0061595 (Antiostatin A4)