NP-MRD: Showing NP-Card for (1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate (NP0229646)

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Record Information

Version

2.0

Created at

2022-09-06 09:48:24 UTC

Updated at

2022-09-06 09:48:24 UTC

NP-MRD ID

NP0229646

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate

Description

3-O-acetylgreenwayodendrin belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. (1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate is found in Greenwayodendron suaveolens. Based on a literature review very few articles have been published on 3-O-acetylgreenwayodendrin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062211482D          

 28 32  0  0  1  0            999 V2000
    7.9122    1.7737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1094    1.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5433    2.1835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8728    0.7930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0701    0.6028    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8335   -0.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0307   -0.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4646    0.2222    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2280   -0.5681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7012    1.0126    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1350    1.6126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3323    1.4224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0957    0.6320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4699    1.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6618    0.0320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2661   -0.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4553   -0.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7097   -0.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1435   -0.2922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3187   -0.3114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1103    0.3933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2854    1.1172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1102    1.1364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5392    0.4317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3500    0.2790    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5039    1.2028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3418    2.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0839    1.7896    0.0000 C   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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  1  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  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 17 25  1  0  0  0  0
 13 25  1  0  0  0  0
 10 26  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 61 65  0  0  0  0  0  0  0  0999 V2000
    6.7145   -0.5589   -1.2996 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4472    0.2194   -1.3139 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4130    1.4270   -1.7246 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2321   -0.3015   -0.8896 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0366    0.4545   -0.9107 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0251   -0.1333   -1.8722 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2821   -1.2904   -1.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5208   -0.9657   -0.0322 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7716   -2.0645    0.9425 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0215    0.4030    0.4410 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2558    0.8803    1.6439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1824    1.1256    1.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7344   -0.1696    0.7291 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9556   -1.0710    1.9077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8867   -0.7237   -0.3597 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7513   -1.8187   -0.8664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0451   -1.0565   -0.8848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2587   -0.9736   -1.5123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9761    0.0608   -0.9544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2442    0.5866   -1.1965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6870    1.6517   -0.4499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8968    2.1898    0.5173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6519    1.6742    0.7555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1769    0.6014    0.0204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0123   -0.0876    0.0486 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4766    0.5483    0.5051 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2232   -0.3402    1.4367 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7474    1.9866    0.9790 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1354   -0.5637   -0.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4516    0.0135   -1.9121 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5019   -1.5590   -1.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2944    1.4576   -1.3094 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.5088   -2.7406 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3105    0.6028   -2.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5707   -1.6584   -2.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0401   -2.1038   -1.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5137   -2.8252    0.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1057   -1.7664    1.9317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1817   -2.6708    0.9990 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6894    1.1052   -0.3901 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3531    0.2561    2.5277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7052    1.8730    1.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7410    1.5429    2.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1228    1.8835    0.3820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4072   -2.0559    1.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1074   -1.1519    2.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7701   -0.5709    2.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8974    0.0719   -1.1709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4517   -2.1406   -1.8666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8820   -2.6821   -0.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6434   -1.5913   -2.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8268    0.1312   -1.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6812    2.0311   -0.6706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2580    3.0391    1.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0193    2.0869    1.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8281   -0.1888    2.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2792    0.0679    1.4888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3324   -1.3781    1.1298 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7690    2.2408    0.6303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7481    2.0628    2.0707 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0487    2.6954    0.4809 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  1
  8 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 13  1  0
 13 14  1  1
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10 26  1  0
 26 27  1  0
 26 28  1  0
 26  5  1  0
 10  8  1  0
 13 15  1  0
 25 17  1  0
 24 19  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  5 32  1  6
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  9 37  1  0
  9 38  1  0
  9 39  1  0
 15 48  1  6
 16 49  1  0
 16 50  1  0
 18 51  1  0
 20 52  1  0
 21 53  1  0
 22 54  1  0
 23 55  1  0
 14 45  1  0
 14 46  1  0
 14 47  1  0
 12 43  1  0
 12 44  1  0
 11 41  1  0
 11 42  1  0
 10 40  1  6
 27 56  1  0
 27 57  1  0
 27 58  1  0
 28 59  1  0
 28 60  1  0
 28 61  1  0
M  END


  Mrv1652309062211482D          

 28 32  0  0  1  0            999 V2000
    7.9122    1.7737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1094    1.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5433    2.1835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8728    0.7930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0701    0.6028    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8335   -0.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0307   -0.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4646    0.2222    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2280   -0.5681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7012    1.0126    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1350    1.6126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3323    1.4224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0957    0.6320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4699    1.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6618    0.0320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2661   -0.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4553   -0.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7097   -0.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1435   -0.2922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3187   -0.3114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1103    0.3933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2854    1.1172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1102    1.1364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5392    0.4317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3500    0.2790    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5039    1.2028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3418    2.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0839    1.7896    0.0000 C   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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  1  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  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 17 25  1  0  0  0  0
 13 25  1  0  0  0  0
 10 26  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0229646

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC4=CC5=CC=CC=C5N4[C@]3(C)CC[C@H]2C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H33NO2/c1-16(27)28-22-11-12-24(4)20(23(22,2)3)10-13-25(5)21(24)15-18-14-17-8-6-7-9-19(17)26(18)25/h6-9,14,20-22H,10-13,15H2,1-5H3/t20-,21+,22-,24-,25+/m0/s1

> <INCHI_KEY>
DRMMGUOJBQDCMO-LJDQNPOQSA-N

> <FORMULA>
C25H33NO2

> <MOLECULAR_WEIGHT>
379.544

> <EXACT_MASS>
379.251129307

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
45.52736397823436

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,12R,13S,16S,18R)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0^{2,10}.0^{3,8}.0^{13,18}]icosa-3,5,7,9-tetraen-16-yl acetate

> <JCHEM_LOGP>
5.206601686

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.003778164551771

> <JCHEM_POLAR_SURFACE_AREA>
31.23

> <JCHEM_REFRACTIVITY>
111.4975

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,12R,13S,16S,18R)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0^{2,10}.0^{3,8}.0^{13,18}]icosa-3,5,7,9-tetraen-16-yl acetate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      14.769   3.311   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.271   2.956   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      12.214   4.076   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      12.829   1.480   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.331   1.125   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.889  -0.350   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.391  -0.705   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.334   0.415   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.892  -1.060   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.776   1.890   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.719   3.010   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.220   2.655   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.779   1.180   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.610   2.183   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.835   0.060   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.097  -1.292   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.583  -1.007   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.191  -1.666   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.135  -0.545   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.595  -0.581   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.206   0.734   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.533   2.085   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.072   2.121   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.873   0.806   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       4.387   0.521   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      10.274   2.245   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.971   3.755   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.357   3.341   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   26                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   15                                             
CONECT    9    8                                                            
CONECT   10    8   11   26                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   25                                             
CONECT   14   13                                                            
CONECT   15   13    8   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19   25                                                  
CONECT   25   24   17   13                                                  
CONECT   26   10    5   27   28                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₃NO₂

Average Mass

379.5440 Da

Monoisotopic Mass

379.25113 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC4=CC5=CC=CC=C5N4[C@]3(C)CC[C@H]2C1(C)C

InChI Identifier

InChI=1S/C25H33NO2/c1-16(27)28-22-11-12-24(4)20(23(22,2)3)10-13-25(5)21(24)15-18-14-17-8-6-7-9-19(17)26(18)25/h6-9,14,20-22H,10-13,15H2,1-5H3/t20-,21+,22-,24-,25+/m0/s1

InChI Key

DRMMGUOJBQDCMO-LJDQNPOQSA-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

Species Name	Source	Reference
Greenwayodendron suaveolens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

Indoles

Alternative Parents

Substituents

Indole
Pyrrolizine
Benzenoid
Heteroaromatic compound
Pyrrole
Carboxylic acid ester
Azacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Carbonyl group
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

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

24675656

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46891355

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate (NP0229646)

MOL for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)

3D MOL for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)

3D SDF for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)

3D-SDF for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)

PDB for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)

3D PDB for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)

SMILES for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)

INCHI for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)

Structure for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)

3D Structure for NP0229646 ((1r,12r,13s,16s,18r)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.0²,¹⁰.0³,⁸.0¹³,¹⁸]icosa-3,5,7,9-tetraen-16-yl acetate)