NP-MRD: Showing NP-Card for 2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid (NP0312437)

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Record Information

Version

2.0

Created at

2022-09-11 09:13:27 UTC

Updated at

2022-09-11 09:13:27 UTC

NP-MRD ID

NP0312437

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

Description

2-(2-Hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1H-indole-5-carboximidic acid belongs to the class of organic compounds known as indolecarboxamides and derivatives. Indolecarboxamides and derivatives are compounds containing a carboxamide group attached to an indole. Based on a literature review very few articles have been published on 2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1H-indole-5-carboximidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112211132D          

 31 33  0  0  0  0            999 V2000
    0.5433    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433    0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9962   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2337   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462   -2.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2337    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8675    2.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2544    2.7371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6744    2.3566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0869    1.6421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5349    1.0290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7064    0.2220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 N   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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  4 13  1  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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  2  0  0  0  0
 17 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 15 30  1  0  0  0  0
 30 31  1  0  0  0  0
 13 31  1  0  0  0  0
M  END

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
   -3.7470   -0.6299   -4.1433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3774   -0.2422   -2.8698 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901   -0.9241   -2.3825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8479   -0.5443   -1.0093 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6924   -1.3296   -0.7152 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8172   -0.8936    0.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1268   -0.2146   -0.1101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0899   -0.5220    0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4877   -1.9196    1.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5707    0.4592    1.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5438    0.2460    2.8186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1488    1.8808    1.4398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4164    0.8976   -0.8705 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1587    1.1927   -1.6340 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9400    0.8867   -0.6763 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2925    0.6967   -0.9113 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1161    0.4245    0.1507 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5413    0.2203   -0.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0872    0.2961   -1.3350 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3361   -0.0368    0.9158 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7296   -0.2393    0.7254 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3870   -1.3087    1.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8109   -2.3875    1.8081 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8288   -1.2255    0.7873 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0159    0.2575    0.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6792    0.6604    0.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4010    1.5764   -0.7421 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6258    0.3376    1.4351 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2881    0.5287    1.6421 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4158    0.8083    0.5838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9782    1.0409    0.5253 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9435   -0.4776   -4.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8900   -1.7496   -4.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7061   -0.1862   -4.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4503   -0.7580   -3.0913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4722   -2.0357   -2.3721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2291   -1.5862   -1.5521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9650   -1.9935    0.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3454   -0.6026    1.0444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0296    0.8586   -0.3254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5943   -0.7029   -1.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0885   -2.3068    2.1830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1289   -2.6178    0.4400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5868   -2.0565    1.2722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1274    1.1730    2.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9806    0.0620    3.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1939   -0.5935    2.5567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0226    1.8998    1.4280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4751    2.5516    2.2329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5126    2.1821    0.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2343    1.5967   -1.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0650    2.2836   -1.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0615    0.5784   -2.5269 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7084    0.7581   -1.9058 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8617    1.0426   -1.9761 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2331   -2.3034    2.6178 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4632   -1.5873    1.6296 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0354   -1.8202   -0.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7992    0.4269   -0.2203 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2762    0.7057    1.5242 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2792    0.1216    2.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8337    0.4737    2.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5899    1.2699    1.3037 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  1
  4  6  1  0
  6  7  1  0
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  8  9  1  0
  8 10  2  3
 10 11  1  0
 10 12  1  0
  4 13  1  0
 13 14  1  0
 14 15  1  0
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 16 17  1  0
 17 28  2  0
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 29 30  2  0
 30 31  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 31 13  1  0
 26 21  1  0
 30 15  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
  9 42  1  0
  9 43  1  0
  9 44  1  0
 11 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 12 50  1  0
 13 51  1  6
 14 52  1  0
 14 53  1  0
 16 54  1  0
 28 61  1  0
 29 62  1  0
 31 63  1  0
 19 55  1  0
 23 56  1  0
 24 57  1  0
 24 58  1  0
 25 59  1  0
 25 60  1  0
M  END


  Mrv1652309112211132D          

 31 33  0  0  0  0            999 V2000
    0.5433    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433    0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9962   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2337   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462   -2.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2337    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8675    2.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2544    2.7371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6744    2.3566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0869    1.6421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5349    1.0290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7064    0.2220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 N   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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  4 13  1  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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  2  0  0  0  0
 17 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 15 30  1  0  0  0  0
 30 31  1  0  0  0  0
 13 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0312437

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COCC(O)(CCC(C)=C(C)C)C1CC2=CC(=CC=C2N1)C(O)=NC1=C(O)CCC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H32N2O5/c1-14(2)15(3)9-10-24(30,13-31-4)21-12-17-11-16(5-6-18(17)25-21)23(29)26-22-19(27)7-8-20(22)28/h5-6,11,21,25,27,30H,7-10,12-13H2,1-4H3,(H,26,29)

> <INCHI_KEY>
BJIBMMAMDZHYDD-UHFFFAOYSA-N

> <FORMULA>
C24H32N2O5

> <MOLECULAR_WEIGHT>
428.529

> <EXACT_MASS>
428.231122138

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
47.961438604836054

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1H-indole-5-carboximidic acid

> <JCHEM_LOGP>
2.708210504666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.418161074298203

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.089618109288916

> <JCHEM_PKA_STRONGEST_BASIC>
2.6583141849648695

> <JCHEM_POLAR_SURFACE_AREA>
111.38

> <JCHEM_REFRACTIVITY>
123.87229999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1H-indole-5-carboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       1.014   2.547   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.014   1.007   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.320   0.237   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.320  -1.303   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.320  -2.843   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.860  -1.303   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.630  -2.637   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.170  -2.637   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.940  -3.970   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.940  -1.303   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.480  -1.303   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.170   0.031   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.591   0.237   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.925  -0.533   0.000  0.00  0.00           O+0
HETATM   20  N   UNK     0       7.591   1.777   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       8.925   2.547   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.086   4.079   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.941   5.109   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.592   4.399   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.362   3.065   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.332   1.921   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.652   0.414   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       2.126  -2.549   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6   13                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    4   14   31                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   30                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   28                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21   27                                                  
CONECT   27   26                                                            
CONECT   28   17   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   15   31                                                  
CONECT   31   30   13                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
2-(2-Hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1H-indole-5-carboximidate	Generator

Chemical Formula

C₂₄H₃₂N₂O₅

Average Mass

428.5290 Da

Monoisotopic Mass

428.23112 Da

IUPAC Name

2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1H-indole-5-carboximidic acid

Traditional Name

2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1H-indole-5-carboximidic acid

CAS Registry Number

Not Available

SMILES

COCC(O)(CCC(C)=C(C)C)C1CC2=CC(=CC=C2N1)C(O)=NC1=C(O)CCC1=O

InChI Identifier

InChI=1S/C24H32N2O5/c1-14(2)15(3)9-10-24(30,13-31-4)21-12-17-11-16(5-6-18(17)25-21)23(29)26-22-19(27)7-8-20(22)28/h5-6,11,21,25,27,30H,7-10,12-13H2,1-4H3,(H,26,29)

InChI Key

BJIBMMAMDZHYDD-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 indolecarboxamides and derivatives. Indolecarboxamides and derivatives are compounds containing a carboxamide group attached to an indole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indolecarboxylic acids and derivatives

Direct Parent

Indolecarboxamides and derivatives

Alternative Parents

Substituents

Indolecarboxamide derivative
Dihydroindole
Aralkylamine
Secondary aliphatic/aromatic amine
Benzenoid
Vinylogous acid
Tertiary alcohol
Cyclic ketone
Secondary carboxylic acid amide
Ketone
Carboxamide group
Amino acid or derivatives
1,2-aminoalcohol
Azacycle
Secondary amine
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
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	2.71	ChemAxon
pKa (Strongest Acidic)	7.09	ChemAxon
pKa (Strongest Basic)	2.66	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	111.38 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	123.87 m³·mol⁻¹	ChemAxon
Polarizability	47.96 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

163049153

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid (NP0312437)

MOL for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)

3D MOL for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)

3D SDF for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)

3D-SDF for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)

PDB for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)

3D PDB for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)

SMILES for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)

INCHI for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)

Structure for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)

3D Structure for NP0312437 (2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid)