NP-MRD: Showing NP-Card for Oxopropaline G (NP0022839)

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Record Information

Version

2.0

Created at

2021-01-06 08:00:19 UTC

Updated at

2021-07-15 17:40:08 UTC

NP-MRD ID

NP0022839

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Oxopropaline G

Provided By

NPAtlas

Description

Oxopropaline G is found in Streptomyces. Based on a literature review very few articles have been published on 3-hydroxy-1-{4-methyl-9H-pyrido[3,4-b]indol-1-yl}propan-1-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105373D          

 33 35  0  0  0  0            999 V2000
   -2.3165    2.5958   -1.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0756    1.7965   -0.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1540    2.3016   -1.1994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2867    1.6208   -1.0063 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2757    0.3973   -0.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5288   -0.3158   -0.2053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5782   -1.4278    0.3390 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8048    0.2901   -0.6675 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9728   -0.5935   -0.3787 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0647   -0.8126    1.0048 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0868   -0.1736    0.0348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2062   -1.3372    0.6481 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5344   -1.4010    0.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3587   -2.3476    1.4219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -2.1151    1.4792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2566   -0.9546    0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4416    0.0005    0.3971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0969   -0.2326    0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0805    0.5667   -0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0251    2.1320   -1.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8143    2.9153   -0.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0074    3.5584   -1.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1689    3.2793   -1.6854 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7670    0.4448   -1.7818 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9085    1.2848   -0.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8970   -0.0994   -0.7176 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8951   -1.5542   -0.8867 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7206   -1.7016    1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4763   -2.0781    0.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9576   -3.2728    1.8291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4067   -2.8423    1.9272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3481   -0.7945    1.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9454    0.8705    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  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  2  1  0  0  0  0
 19 11  2  0  0  0  0
 18 13  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  3 23  1  0  0  0  0
  8 24  1  0  0  0  0
  8 25  1  0  0  0  0
  9 26  1  0  0  0  0
  9 27  1  0  0  0  0
 10 28  1  0  0  0  0
 12 29  1  0  0  0  0
 14 30  1  0  0  0  0
 15 31  1  0  0  0  0
 16 32  1  0  0  0  0
 17 33  1  0  0  0  0
M  END

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -2.3165    2.5958   -1.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0756    1.7965   -0.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1540    2.3016   -1.1994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2867    1.6208   -1.0063 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2757    0.3973   -0.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5288   -0.3158   -0.2053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5782   -1.4278    0.3390 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8048    0.2901   -0.6675 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9728   -0.5935   -0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0647   -0.8126    1.0048 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0868   -0.1736    0.0348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2062   -1.3372    0.6481 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5344   -1.4010    0.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3587   -2.3476    1.4219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -2.1151    1.4792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2566   -0.9546    0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4416    0.0005    0.3971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0969   -0.2326    0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0805    0.5667   -0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0251    2.1320   -1.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8143    2.9153   -0.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0074    3.5584   -1.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1689    3.2793   -1.6854 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7670    0.4448   -1.7818 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9085    1.2848   -0.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8970   -0.0994   -0.7176 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8951   -1.5542   -0.8867 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7206   -1.7016    1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4763   -2.0781    0.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9576   -3.2728    1.8291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4067   -2.8423    1.9272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3481   -0.7945    1.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9454    0.8705    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
  5 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19  2  1  0
 19 11  2  0
 18 13  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 16 32  1  0
 17 33  1  0
M  END


  Mrv1652306242105373D          

 33 35  0  0  0  0            999 V2000
   -2.3165    2.5958   -1.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0756    1.7965   -0.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1540    2.3016   -1.1994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2867    1.6208   -1.0063 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2757    0.3973   -0.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5288   -0.3158   -0.2053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5782   -1.4278    0.3390 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8048    0.2901   -0.6675 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9728   -0.5935   -0.3787 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0647   -0.8126    1.0048 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0868   -0.1736    0.0348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2062   -1.3372    0.6481 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5344   -1.4010    0.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3587   -2.3476    1.4219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -2.1151    1.4792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2566   -0.9546    0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4416    0.0005    0.3971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0969   -0.2326    0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0805    0.5667   -0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0251    2.1320   -1.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8143    2.9153   -0.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0074    3.5584   -1.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1689    3.2793   -1.6854 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7670    0.4448   -1.7818 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9085    1.2848   -0.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8970   -0.0994   -0.7176 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8951   -1.5542   -0.8867 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7206   -1.7016    1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4763   -2.0781    0.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9576   -3.2728    1.8291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4067   -2.8423    1.9272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3481   -0.7945    1.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9454    0.8705    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  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  2  1  0  0  0  0
 19 11  2  0  0  0  0
 18 13  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  3 23  1  0  0  0  0
  8 24  1  0  0  0  0
  8 25  1  0  0  0  0
  9 26  1  0  0  0  0
  9 27  1  0  0  0  0
 10 28  1  0  0  0  0
 12 29  1  0  0  0  0
 14 30  1  0  0  0  0
 15 31  1  0  0  0  0
 16 32  1  0  0  0  0
 17 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0022839

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])C([H])([H])C(=O)C1=NC([H])=C(C2=C1N([H])C1=C([H])C([H])=C([H])C([H])=C21)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H14N2O2/c1-9-8-16-14(12(19)6-7-18)15-13(9)10-4-2-3-5-11(10)17-15/h2-5,8,17-18H,6-7H2,1H3

> <INCHI_KEY>
LXWBBBQUPXDVAN-UHFFFAOYSA-N

> <FORMULA>
C15H14N2O2

> <MOLECULAR_WEIGHT>
254.289

> <EXACT_MASS>
254.105527699

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
27.707853739933334

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-hydroxy-1-{4-methyl-9H-pyrido[3,4-b]indol-1-yl}propan-1-one

> <ALOGPS_LOGP>
1.94

> <JCHEM_LOGP>
1.749897186333333

> <ALOGPS_LOGS>
-3.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.655290665514851

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.880265006413993

> <JCHEM_PKA_STRONGEST_BASIC>
3.403930453475113

> <JCHEM_POLAR_SURFACE_AREA>
65.97999999999999

> <JCHEM_REFRACTIVITY>
72.7889

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.94e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-1-{4-methyl-9H-pyrido[3,4-b]indol-1-yl}propan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -2.3165    2.5958   -1.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0756    1.7965   -0.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1540    2.3016   -1.1994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2867    1.6208   -1.0063 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2757    0.3973   -0.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5288   -0.3158   -0.2053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5782   -1.4278    0.3390 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8048    0.2901   -0.6675 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9728   -0.5935   -0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0647   -0.8126    1.0048 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0868   -0.1736    0.0348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2062   -1.3372    0.6481 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5344   -1.4010    0.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3587   -2.3476    1.4219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -2.1151    1.4792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2566   -0.9546    0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4416    0.0005    0.3971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0969   -0.2326    0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0805    0.5667   -0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0251    2.1320   -1.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8143    2.9153   -0.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0074    3.5584   -1.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1689    3.2793   -1.6854 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7670    0.4448   -1.7818 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9085    1.2848   -0.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8970   -0.0994   -0.7176 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8951   -1.5542   -0.8867 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7206   -1.7016    1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4763   -2.0781    0.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9576   -3.2728    1.8291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4067   -2.8423    1.9272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3481   -0.7945    1.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9454    0.8705    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
  5 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19  2  1  0
 19 11  2  0
 18 13  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 16 32  1  0
 17 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      -2.317   2.596  -1.031  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.076   1.797  -0.793  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.154   2.302  -1.199  0.00  0.00           C+0
HETATM    4  N   UNK     0       1.287   1.621  -1.006  0.00  0.00           N+0
HETATM    5  C   UNK     0       1.276   0.397  -0.399  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.529  -0.316  -0.205  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.578  -1.428   0.339  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.805   0.290  -0.668  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.973  -0.594  -0.379  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.065  -0.813   1.005  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.087  -0.174   0.035  0.00  0.00           C+0
HETATM   12  N   UNK     0      -0.206  -1.337   0.648  0.00  0.00           N+0
HETATM   13  C   UNK     0      -1.534  -1.401   0.849  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.359  -2.348   1.422  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.714  -2.115   1.479  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.257  -0.955   0.974  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.442   0.001   0.397  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.097  -0.233   0.342  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.081   0.567  -0.183  0.00  0.00           C+0
HETATM   20  H   UNK     0      -3.025   2.132  -1.712  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.814   2.915  -0.098  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.007   3.558  -1.522  0.00  0.00           H+0
HETATM   23  H   UNK     0       0.169   3.279  -1.685  0.00  0.00           H+0
HETATM   24  H   UNK     0       3.767   0.445  -1.782  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.909   1.285  -0.205  0.00  0.00           H+0
HETATM   26  H   UNK     0       5.897  -0.099  -0.718  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.895  -1.554  -0.887  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.721  -1.702   1.236  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.476  -2.078   0.928  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.958  -3.273   1.829  0.00  0.00           H+0
HETATM   31  H   UNK     0      -4.407  -2.842   1.927  0.00  0.00           H+0
HETATM   32  H   UNK     0      -5.348  -0.795   1.033  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.945   0.871   0.030  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    1    3   19                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   24   25                                             
CONECT    9    8   10   26   27                                             
CONECT   10    9   28                                                       
CONECT   11    5   12   19                                                  
CONECT   12   11   13   29                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15   30                                                  
CONECT   15   14   16   31                                                  
CONECT   16   15   17   32                                                  
CONECT   17   16   18   33                                                  
CONECT   18   17   19   13                                                  
CONECT   19   18    2   11                                                  
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    3                                                            
CONECT   24    8                                                            
CONECT   25    8                                                            
CONECT   26    9                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   12                                                            
CONECT   30   14                                                            
CONECT   31   15                                                            
CONECT   32   16                                                            
CONECT   33   17                                                            
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
   -2.3165    2.5958   -1.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0756    1.7965   -0.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1540    2.3016   -1.1994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2867    1.6208   -1.0063 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2757    0.3973   -0.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5288   -0.3158   -0.2053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5782   -1.4278    0.3390 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8048    0.2901   -0.6675 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9728   -0.5935   -0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0647   -0.8126    1.0048 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0868   -0.1736    0.0348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2062   -1.3372    0.6481 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5344   -1.4010    0.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3587   -2.3476    1.4219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -2.1151    1.4792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2566   -0.9546    0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4416    0.0005    0.3971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0969   -0.2326    0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0805    0.5667   -0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0251    2.1320   -1.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8143    2.9153   -0.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0074    3.5584   -1.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1689    3.2793   -1.6854 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7670    0.4448   -1.7818 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9085    1.2848   -0.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8970   -0.0994   -0.7176 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8951   -1.5542   -0.8867 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7206   -1.7016    1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4763   -2.0781    0.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9576   -3.2728    1.8291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4067   -2.8423    1.9272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3481   -0.7945    1.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9454    0.8705    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
  5 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19  2  1  0
 19 11  2  0
 18 13  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 16 32  1  0
 17 33  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₅H₁₄N₂O₂

Average Mass

254.2890 Da

Monoisotopic Mass

254.10553 Da

IUPAC Name

3-hydroxy-1-{4-methyl-9H-pyrido[3,4-b]indol-1-yl}propan-1-one

Traditional Name

3-hydroxy-1-{4-methyl-9H-pyrido[3,4-b]indol-1-yl}propan-1-one

CAS Registry Number

Not Available

SMILES

CC1=CN=C(C(=O)CCO)C2=C1C1=CC=CC=C1N2

InChI Identifier

InChI=1S/C15H14N2O2/c1-9-8-16-14(12(19)6-7-18)15-13(9)10-4-2-3-5-11(10)17-15/h2-5,8,17-18H,6-7H2,1H3

InChI Key

LXWBBBQUPXDVAN-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	NPAtlas	8270489

Species Where Detected

Species Name	Source	Reference
Streptomyces sp. G324	KNApSAcK Database	22123792

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as harmala alkaloids. These are compounds with a structure based on harmaline, harmine, harmalol, harman or a derivative of those parents. These parents are beta-carbolines, consisting of a pyrimidine fused to the pyrrole moiety of an indole to form a pyrido[3,4-b]indole.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Harmala alkaloids

Sub Class

Not Available

Direct Parent

Harmala alkaloids

Alternative Parents

Substituents

Harman
Beta-carboline
Pyridoindole
Indole
Indole or derivatives
Aryl ketone
Aryl alkyl ketone
Methylpyridine
Beta-hydroxy ketone
Pyridine
Benzenoid
Heteroaromatic compound
Pyrrole
Vinylogous amide
Ketone
Azacycle
Organoheterocyclic compound
Alcohol
Primary alcohol
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
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	1.94	ALOGPS
logP	1.75	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	11.88	ChemAxon
pKa (Strongest Basic)	3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	65.98 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	72.79 m³·mol⁻¹	ChemAxon
Polarizability	27.71 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

NPA000341

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00016908

Chemspider ID

139696

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Oxopropaline G (NP0022839)

MOL for NP0022839 (Oxopropaline G)

3D MOL for NP0022839 (Oxopropaline G)

3D SDF for NP0022839 (Oxopropaline G)

3D-SDF for NP0022839 (Oxopropaline G)

PDB for NP0022839 (Oxopropaline G)

3D PDB for NP0022839 (Oxopropaline G)

SMILES for NP0022839 (Oxopropaline G)

INCHI for NP0022839 (Oxopropaline G)

Structure for NP0022839 (Oxopropaline G)

3D Structure for NP0022839 (Oxopropaline G)