NP-MRD: Showing NP-Card for Carbazomycin B (NP0022175)

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Record Information

Version

1.0

Created at

2021-01-06 07:24:08 UTC

Updated at

2021-07-15 17:38:20 UTC

NP-MRD ID

NP0022175

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Carbazomycin B

Provided By

NPAtlas

Description

Carbazomycin B is found in Streptomyces abikoensis, Streptomyces ehimensis, Streptomyces luteoverticillatus and Streptomyces sp.. It was first documented in 1980 (PMID: 7440417). Based on a literature review very few articles have been published on 3-methoxy-1,2-dimethyl-9H-carbazol-4-ol (PMID: 31168648) (PMID: 25296703) (PMID: 33841348).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105213D          

 33 35  0  0  0  0            999 V2000
   -2.7820    2.9871    0.4062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4544    2.1054   -0.6691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6039    1.0203   -0.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0780   -0.1929   -0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5696   -0.3680    0.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2180   -1.2407    0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7424   -2.5623    0.6911 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1531   -1.0525    0.1121 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1874   -1.9007    0.3001 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3321   -1.2685    0.0347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542   -1.6497    0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6217   -0.7336   -0.2763 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3201    0.5565   -0.6454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9806    0.9347   -0.6718 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0012    0.0430   -0.3390 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6122    0.1926   -0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2237    1.2636   -0.5613 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1801    2.5005   -0.9606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8594    3.2366    0.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2426    3.9698    0.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5481    2.5474    1.3918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0028    0.6162    0.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7552   -1.0636    0.9684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0117   -0.7871   -0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8900   -3.2000    1.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2975   -3.0363   -0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4205   -2.4843    1.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1429   -2.8981    0.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9425   -2.6618    0.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6782   -1.0424   -0.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.2655   -0.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8098    1.9379   -0.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9763    2.9652   -1.1527 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
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  9 10  1  0  0  0  0
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 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17  3  1  0  0  0  0
 16  8  1  0  0  0  0
 15 10  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  5 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  7 27  1  0  0  0  0
  9 28  1  0  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 14 32  1  0  0  0  0
 18 33  1  0  0  0  0
M  END

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -2.7820    2.9871    0.4062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4544    2.1054   -0.6691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6039    1.0203   -0.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0780   -0.1929   -0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5696   -0.3680    0.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2180   -1.2407    0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7424   -2.5623    0.6911 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1531   -1.0525    0.1121 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1874   -1.9007    0.3001 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3321   -1.2685    0.0347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542   -1.6497    0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6217   -0.7336   -0.2763 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3201    0.5565   -0.6454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9806    0.9347   -0.6718 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0012    0.0430   -0.3390 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6122    0.1926   -0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2237    1.2636   -0.5613 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1801    2.5005   -0.9606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8594    3.2366    0.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2426    3.9698    0.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5481    2.5474    1.3918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0028    0.6162    0.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7552   -1.0636    0.9684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0117   -0.7871   -0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8900   -3.2000    1.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2975   -3.0363   -0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4205   -2.4843    1.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1429   -2.8981    0.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9425   -2.6618    0.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6782   -1.0424   -0.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.2655   -0.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8098    1.9379   -0.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9763    2.9652   -1.1527 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17  3  1  0
 16  8  1  0
 15 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  5 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  9 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 18 33  1  0
M  END


  Mrv1652306242105213D          

 33 35  0  0  0  0            999 V2000
   -2.7820    2.9871    0.4062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4544    2.1054   -0.6691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6039    1.0203   -0.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0780   -0.1929   -0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5696   -0.3680    0.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2180   -1.2407    0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7424   -2.5623    0.6911 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1531   -1.0525    0.1121 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1874   -1.9007    0.3001 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3321   -1.2685    0.0347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542   -1.6497    0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6217   -0.7336   -0.2763 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3201    0.5565   -0.6454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9806    0.9347   -0.6718 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0012    0.0430   -0.3390 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6122    0.1926   -0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2237    1.2636   -0.5613 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1801    2.5005   -0.9606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8594    3.2366    0.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2426    3.9698    0.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5481    2.5474    1.3918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0028    0.6162    0.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7552   -1.0636    0.9684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0117   -0.7871   -0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8900   -3.2000    1.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2975   -3.0363   -0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4205   -2.4843    1.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1429   -2.8981    0.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9425   -2.6618    0.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6782   -1.0424   -0.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.2655   -0.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8098    1.9379   -0.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9763    2.9652   -1.1527 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17  3  1  0  0  0  0
 16  8  1  0  0  0  0
 15 10  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  5 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  7 27  1  0  0  0  0
  9 28  1  0  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 14 32  1  0  0  0  0
 18 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0022175

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C3=C([H])C([H])=C([H])C([H])=C3N([H])C2=C(C(=C1OC([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H15NO2/c1-8-9(2)15(18-3)14(17)12-10-6-4-5-7-11(10)16-13(8)12/h4-7,16-17H,1-3H3

> <INCHI_KEY>
OBMFXFPFPDTBHG-UHFFFAOYSA-N

> <FORMULA>
C15H15NO2

> <MOLECULAR_WEIGHT>
241.29

> <EXACT_MASS>
241.110278727

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
27.14894462102177

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-methoxy-1,2-dimethyl-9H-carbazol-4-ol

> <ALOGPS_LOGP>
3.39

> <JCHEM_LOGP>
3.656491880666667

> <ALOGPS_LOGS>
-3.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.67924425527507

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.914902329477849

> <JCHEM_PKA_STRONGEST_BASIC>
-4.910015256326936

> <JCHEM_POLAR_SURFACE_AREA>
45.25

> <JCHEM_REFRACTIVITY>
71.9987

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.60e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-methoxy-1,2-dimethyl-9H-carbazol-4-ol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -2.7820    2.9871    0.4062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4544    2.1054   -0.6691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6039    1.0203   -0.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0780   -0.1929   -0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5696   -0.3680    0.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2180   -1.2407    0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7424   -2.5623    0.6911 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1531   -1.0525    0.1121 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1874   -1.9007    0.3001 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3321   -1.2685    0.0347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542   -1.6497    0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6217   -0.7336   -0.2763 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3201    0.5565   -0.6454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9806    0.9347   -0.6718 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0012    0.0430   -0.3390 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6122    0.1926   -0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2237    1.2636   -0.5613 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1801    2.5005   -0.9606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8594    3.2366    0.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2426    3.9698    0.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5481    2.5474    1.3918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0028    0.6162    0.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7552   -1.0636    0.9684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0117   -0.7871   -0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8900   -3.2000    1.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2975   -3.0363   -0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4205   -2.4843    1.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1429   -2.8981    0.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9425   -2.6618    0.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6782   -1.0424   -0.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.2655   -0.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8098    1.9379   -0.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9763    2.9652   -1.1527 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17  3  1  0
 16  8  1  0
 15 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  5 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  9 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 18 33  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.782   2.987   0.406  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.454   2.105  -0.669  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.604   1.020  -0.398  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.078  -0.193  -0.001  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.570  -0.368   0.149  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.218  -1.241   0.259  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.742  -2.562   0.691  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.153  -1.052   0.112  0.00  0.00           C+0
HETATM    9  N   UNK     0       1.187  -1.901   0.300  0.00  0.00           N+0
HETATM   10  C   UNK     0       2.332  -1.268   0.035  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.654  -1.650   0.063  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.622  -0.734  -0.276  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.320   0.557  -0.645  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.981   0.935  -0.672  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.001   0.043  -0.339  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.612   0.193  -0.293  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.224   1.264  -0.561  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.180   2.501  -0.961  0.00  0.00           O+0
HETATM   19  H   UNK     0      -3.859   3.237   0.393  0.00  0.00           H+0
HETATM   20  H   UNK     0      -2.243   3.970   0.267  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.548   2.547   1.392  0.00  0.00           H+0
HETATM   22  H   UNK     0      -4.003   0.616   0.425  0.00  0.00           H+0
HETATM   23  H   UNK     0      -3.755  -1.064   0.968  0.00  0.00           H+0
HETATM   24  H   UNK     0      -4.012  -0.787  -0.766  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.890  -3.200   1.012  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.297  -3.036  -0.136  0.00  0.00           H+0
HETATM   27  H   UNK     0      -2.421  -2.484   1.570  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.143  -2.898   0.604  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.942  -2.662   0.349  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.678  -1.042  -0.252  0.00  0.00           H+0
HETATM   31  H   UNK     0       5.107   1.266  -0.911  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.810   1.938  -0.963  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.976   2.965  -1.153  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4   22   23   24                                             
CONECT    6    4    7    8                                                  
CONECT    7    6   25   26   27                                             
CONECT    8    6    9   16                                                  
CONECT    9    8   10   28                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12   29                                                  
CONECT   12   11   13   30                                                  
CONECT   13   12   14   31                                                  
CONECT   14   13   15   32                                                  
CONECT   15   14   16   10                                                  
CONECT   16   15   17    8                                                  
CONECT   17   16   18    3                                                  
CONECT   18   17   33                                                       
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    5                                                            
CONECT   23    5                                                            
CONECT   24    5                                                            
CONECT   25    7                                                            
CONECT   26    7                                                            
CONECT   27    7                                                            
CONECT   28    9                                                            
CONECT   29   11                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   14                                                            
CONECT   33   18                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

RDKit          3D

33 35  0  0  0  0  0  0  0  0999 V2000
   -2.7820    2.9871    0.4062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4544    2.1054   -0.6691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6039    1.0203   -0.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0780   -0.1929   -0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5696   -0.3680    0.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2180   -1.2407    0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7424   -2.5623    0.6911 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1531   -1.0525    0.1121 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1874   -1.9007    0.3001 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3321   -1.2685    0.0347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542   -1.6497    0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6217   -0.7336   -0.2763 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3201    0.5565   -0.6454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9806    0.9347   -0.6718 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0012    0.0430   -0.3390 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6122    0.1926   -0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2237    1.2636   -0.5613 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1801    2.5005   -0.9606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8594    3.2366    0.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2426    3.9698    0.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5481    2.5474    1.3918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0028    0.6162    0.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7552   -1.0636    0.9684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0117   -0.7871   -0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8900   -3.2000    1.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2975   -3.0363   -0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4205   -2.4843    1.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1429   -2.8981    0.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9425   -2.6618    0.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6782   -1.0424   -0.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.2655   -0.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8098    1.9379   -0.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9763    2.9652   -1.1527 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17  3  1  0
 16  8  1  0
 15 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  5 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  9 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 18 33  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
4-Hydroxy-3-methoxy-1,2-dimethylcarbazole	MeSH

Chemical Formula

C₁₅H₁₅NO₂

Average Mass

241.2900 Da

Monoisotopic Mass

241.11028 Da

IUPAC Name

3-methoxy-1,2-dimethyl-9H-carbazol-4-ol

Traditional Name

3-methoxy-1,2-dimethyl-9H-carbazol-4-ol

CAS Registry Number

Not Available

SMILES

COC1=C(O)C2=C(NC3=CC=CC=C23)C(C)=C1C

InChI Identifier

InChI=1S/C15H15NO2/c1-8-9(2)15(18-3)14(17)12-10-6-4-5-7-11(10)16-13(8)12/h4-7,16-17H,1-3H3

InChI Key

OBMFXFPFPDTBHG-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 abikoensis	LOTUS Database	35616633
Streptomyces ehimensis	LOTUS Database	35616633
Streptomyces luteoverticillatus	LOTUS Database	35616633
Streptomyces sp.	NPAtlas	7440417

Species Where Detected

Species Name	Source	Reference
Streptomyces ehimense	KNApSAcK Database	22123792
Streptomyces strain H 1051-MY 10	KNApSAcK Database	22123792
Streptoverticillium sp.	KNApSAcK Database	22123792

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as carbazoles. These 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
Ether
Azacycle
Organonitrogen compound
Hydrocarbon derivative
Organic nitrogen compound
Organopnictogen 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	3.39	ALOGPS
logP	3.66	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	8.91	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	45.25 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	72 m³·mol⁻¹	ChemAxon
Polarizability	27.15 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	No	ChemAxon

External Links

NPAtlas ID

NPA000188

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00018291

Chemspider ID

145689

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

166449

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Sakano K, Nakamura S: New antibiotics, carbazomycins A and B. II. Structural elucidation. J Antibiot (Tokyo). 1980 Sep;33(9):961-6. doi: 10.7164/antibiotics.33.961. [PubMed:7440417 ]
Feng Z, Chen G, Zhang J, Zhu H, Yu X, Yin Y, Zhang X: Characterization and Complete Genome Analysis of the Carbazomycin B-Producing Strain Streptomyces luteoverticillatus SZJ61. Curr Microbiol. 2019 Sep;76(9):982-987. doi: 10.1007/s00284-019-01711-x. Epub 2019 Jun 5. [PubMed:31168648 ]
Markad SB, Argade NP: Diversity oriented convergent access for collective total synthesis of bioactive multifunctional carbazole alkaloids: synthesis of carbazomycin A, carbazomycin B, hyellazole, chlorohyellazole, and clausenaline D. Org Lett. 2014 Oct 17;16(20):5470-3. doi: 10.1021/ol502721r. Epub 2014 Oct 9. [PubMed:25296703 ]
Shi T, Guo X, Zhu J, Hu L, He Z, Jiang D: Inhibitory Effects of Carbazomycin B Produced by Streptomyces roseoverticillatus 63 Against Xanthomonas oryzae pv. oryzae. Front Microbiol. 2021 Mar 24;12:616937. doi: 10.3389/fmicb.2021.616937. eCollection 2021. [PubMed:33841348 ]

Showing NP-Card for Carbazomycin B (NP0022175)

MOL for NP0022175 (Carbazomycin B)

3D MOL for NP0022175 (Carbazomycin B)

3D SDF for NP0022175 (Carbazomycin B)

3D-SDF for NP0022175 (Carbazomycin B)

PDB for NP0022175 (Carbazomycin B)

3D PDB for NP0022175 (Carbazomycin B)

SMILES for NP0022175 (Carbazomycin B)

INCHI for NP0022175 (Carbazomycin B)

Structure for NP0022175 (Carbazomycin B)

3D Structure for NP0022175 (Carbazomycin B)