NP-MRD: Showing NP-Card for 1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol (NP0164598)

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Record Information

Version

2.0

Created at

2022-09-02 23:30:38 UTC

Updated at

2022-09-02 23:30:38 UTC

NP-MRD ID

NP0164598

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol

Description

137714-93-3, Also known as neocarazostatin C, 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. 137714-93-3 Is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161502592D          

 28 30  0  0  0  0            999 V2000
   -0.3502   -4.4985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0953   -3.7139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7117   -3.5424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2637   -4.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0707   -3.9840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0088   -4.9401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9666   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3924   -2.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6695   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1175   -0.7470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3724    0.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314   -0.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0285   -1.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -1.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4056   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2125   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7646   -0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5096    0.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0617    0.6508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8067    1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8686    0.4792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9154   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1085   -2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4410   -3.0712    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736   -2.5862    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
  4  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
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  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
 21 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 16 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  7 28  1  0  0  0  0
 15 28  2  0  0  0  0
M  END

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
   -2.5220   -4.5341    0.9458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2399   -3.3616    1.7103 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9014   -2.2097    1.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8675   -1.3168    0.6160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3026   -1.6580    0.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6114   -0.1331   -0.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7228    0.7162   -0.4167 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4442    1.2794    0.6473 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8061    1.1800    0.5928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5268    1.8103   -1.4576 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2314    3.0995   -0.6793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8460    2.1424   -1.9801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2474    0.1054   -0.3751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6475    1.1115   -1.0173 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6917    0.8341   -1.0108 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7296    1.5429   -1.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0200    1.0447   -1.3997 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2693   -0.1537   -0.7435 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6277   -0.6787   -0.5966 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2483   -0.0706    0.6011 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3624    0.6367    0.4236 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9674    0.8146   -0.9185 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9802    1.2464    1.6147 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2088   -0.8608   -0.2171 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9411   -0.3385   -0.3697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2806   -0.8200    0.0435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -1.9678    0.7338 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4059   -2.8278    1.1109 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7002   -5.2607    1.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4865   -4.9861    1.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5806   -4.3144   -0.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6650   -1.0804    1.7820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3192   -2.7405    1.3004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9005   -1.6434    0.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5281    0.0845   -0.9452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2588    1.6354    1.5294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2357    0.2108    0.3508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2422    1.8730   -0.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9770    1.5947   -2.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7158    3.8213   -1.3436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5282    2.9025    0.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1438    3.5367   -0.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7704    3.0380   -2.4152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0630    1.9412   -1.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5495    2.4666   -2.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8550    1.5938   -1.8095 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2507   -0.5939   -1.5108 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5778   -1.7864   -0.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7853   -0.2204    1.5507 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2375   -0.1848   -1.3291 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2154    1.2645   -1.5904 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8822    1.4047   -0.8118 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9060    2.3587    1.6002 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5237    0.8983    2.5361 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0736    1.0292    1.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3207   -1.7936    0.3032 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2869   -3.6825    1.6113 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7 10  1  0
 10 11  1  0
 10 12  1  0
  7  6  1  0
  6  4  2  0
  4  5  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3 27  2  0
 27 28  1  0
 27 26  1  0
 26 13  2  0
 13 14  1  0
 14 15  1  0
 15 25  2  0
 25 24  1  0
 24 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  2  3
 21 22  1  0
 21 23  1  0
 18 17  1  0
 17 16  2  0
 13  6  1  0
 16 15  1  0
 25 26  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
  7 35  1  6
 10 39  1  6
 11 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
  5 32  1  0
  5 33  1  0
  5 34  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 28 57  1  0
 14 44  1  0
 24 56  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 22 50  1  0
 22 51  1  0
 22 52  1  0
 23 53  1  0
 23 54  1  0
 23 55  1  0
 17 46  1  0
 16 45  1  0
M  END


  Mrv1533004161502592D          

 28 30  0  0  0  0            999 V2000
   -0.3502   -4.4985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0953   -3.7139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7117   -3.5424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2637   -4.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0707   -3.9840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0088   -4.9401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9666   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3924   -2.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6695   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1175   -0.7470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3724    0.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314   -0.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0285   -1.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -1.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4056   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2125   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7646   -0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5096    0.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0617    0.6508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8067    1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8686    0.4792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9154   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1085   -2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4410   -3.0712    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736   -2.5862    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
  4  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
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  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
 21 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 16 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  7 28  1  0  0  0  0
 15 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0164598

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(C(C)O)C1=C(C)C(OC)=C(O)C2=C1NC1=C2C=C(CC=C(C)C)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H29NO4/c1-12(2)7-8-15-9-10-17-16(11-15)19-20(24-17)18(23(28-6)14(4)25)13(3)22(27-5)21(19)26/h7,9-11,14,23-26H,8H2,1-6H3

> <INCHI_KEY>
MOHYRIVKJGNOOE-UHFFFAOYSA-N

> <FORMULA>
C23H29NO4

> <MOLECULAR_WEIGHT>
383.488

> <EXACT_MASS>
383.209658418

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
43.97050472395757

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9H-carbazol-4-ol

> <ALOGPS_LOGP>
3.99

> <JCHEM_LOGP>
4.533654309666666

> <ALOGPS_LOGS>
-4.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.374655269649764

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.657252186522678

> <JCHEM_PKA_STRONGEST_BASIC>
-3.078934933320464

> <JCHEM_POLAR_SURFACE_AREA>
74.71000000000001

> <JCHEM_REFRACTIVITY>
113.14870000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.66e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9H-carbazol-4-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -0.654  -8.397   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.178  -6.933   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.328  -6.612   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.359  -7.757   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.865  -7.437   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.883  -9.222   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.804  -5.148   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.774  -4.003   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.732  -4.324   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.250  -2.539   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.219  -1.394   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.695   0.070   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.756  -2.219   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.232  -0.754   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.787  -3.363   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.327  -3.363   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.357  -2.219   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.863  -2.539   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.894  -1.394   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.418   0.070   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.448   1.215   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.973   2.679   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.955   0.895   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.339  -4.003   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.309  -5.148   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.802  -4.828   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       4.557  -5.733   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       3.311  -4.828   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    7                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4                                                            
CONECT    7    3    8   28                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   28                                                  
CONECT   16   15   17   26                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   18   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   16   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27    7   15                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
Neocarazostatin C	MeSH

Chemical Formula

C₂₃H₂₉NO₄

Average Mass

383.4880 Da

Monoisotopic Mass

383.20966 Da

IUPAC Name

1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9H-carbazol-4-ol

Traditional Name

1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9H-carbazol-4-ol

CAS Registry Number

Not Available

SMILES

COC(C(C)O)C1=C(C)C(OC)=C(O)C2=C1NC1=C2C=C(CC=C(C)C)C=C1

InChI Identifier

InChI=1S/C23H29NO4/c1-12(2)7-8-15-9-10-17-16(11-15)19-20(24-17)18(23(28-6)14(4)25)13(3)22(27-5)21(19)26/h7,9-11,14,23-26H,8H2,1-6H3

InChI Key

MOHYRIVKJGNOOE-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, 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

Not Available

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
Anisole
Alkyl aryl ether
Benzenoid
Heteroaromatic compound
Pyrrole
Secondary alcohol
Dialkyl ether
Ether
Azacycle
Hydrocarbon derivative
Organic nitrogen compound
Alcohol
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Organic oxygen 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	3.99	ALOGPS
logP	4.53	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	8.66	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	74.71 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	113.15 m³·mol⁻¹	ChemAxon
Polarizability	43.97 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

195851

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol (NP0164598)

MOL for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)

3D MOL for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)

3D SDF for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)

3D-SDF for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)

PDB for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)

3D PDB for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)

SMILES for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)

INCHI for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)

Structure for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)

3D Structure for NP0164598 (1-(2-hydroxy-1-methoxypropyl)-3-methoxy-2-methyl-6-(3-methylbut-2-en-1-yl)-9h-carbazol-4-ol)