NP-MRD: Showing NP-Card for (2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene (NP0236894)

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Record Information

Version

2.0

Created at

2022-09-06 19:53:49 UTC

Updated at

2022-09-06 19:53:49 UTC

NP-MRD ID

NP0236894

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene

Description

NSC809592 belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms. (2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene is found in Streptomyces cacaoi. Based on a literature review very few articles have been published on NSC809592.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062221532D          

 30 34  0  0  1  0            999 V2000
    2.2576    0.1410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0242    0.6877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6790    0.2870    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3945    0.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0063    0.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8136    0.3138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1510    1.0667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9713    0.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1409    0.1711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4254   -0.2397    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6689   -0.6086    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8486   -0.5204    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1017   -1.3056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5482   -1.9174    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8012   -2.7026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7416   -1.7439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4886   -0.9587    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6820   -0.7852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1285   -1.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3219   -1.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0689   -0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6224    0.1735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693    0.9587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9228    1.5705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7294    1.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4449    1.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0566    1.2543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7890    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9824    0.6118    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0421   -0.3469    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
  5 11  2  0  0  0  0
 12 11  1  1  0  0  0
  3 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 25 29  1  0  0  0  0
 30 28  1  1  0  0  0
 17 30  1  0  0  0  0
 12 30  1  0  0  0  0
M  END

     RDKit          3D

 65 69  0  0  0  0  0  0  0  0999 V2000
   -1.2624   -4.0629    0.1060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4194   -2.7639    0.5549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1940   -2.0574   -0.3100 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5148   -1.5930    0.3134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1499   -0.2403    0.7950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8875    0.5229    1.8358 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.5142    2.1187    3.2650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3855    1.0531    3.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5837   -0.7623   -0.7867 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2562   -0.4763   -1.9943 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0046    0.6982   -2.5875 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6741    1.9063   -1.9877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5016    0.9493   -2.7974 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1361    0.7442   -1.5082 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5652    0.9034   -1.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3046    2.1878   -1.3957 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3284    2.1755   -0.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5767    1.4864   -0.4489 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9185    0.1724    0.0841 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7410   -0.1834    1.5008 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0110   -1.5371    1.7334 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5613   -1.3917    1.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5413   -0.9906    2.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4461   -0.7837    1.3883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7989   -1.0557    0.0590 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0927   -1.4330    0.0336 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340   -0.7678   -1.0601 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2568   -4.5641    0.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6455   -4.6973    0.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4889   -2.7244   -1.1438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3154   -1.5114   -0.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7916   -2.2194    1.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7600    2.3751    1.9814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5350    3.0646    3.8260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2364    1.0102    4.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5017   -0.8063    2.3878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4053    0.6208   -3.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5554    1.6455   -1.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0747    2.5996   -2.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0066    2.5222   -1.3697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4300    2.0159   -3.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1403    0.3170   -3.6310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4881    1.2945   -0.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1221    0.1840   -1.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6350    0.7144   -0.1404 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6928    3.0840   -1.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9120    2.2565   -2.3251 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4750    3.2332    0.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7739    1.7380    0.6313 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4119    2.1996   -0.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7581    1.4165   -1.5747 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0603    0.0773   -0.1037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5681   -0.6090   -0.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6973   -0.2996    2.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1895    0.6058    2.0982 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0181   -1.7116    2.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6234   -2.2883    1.3367 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5993   -0.8661    3.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5476   -0.4558    1.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6526   -1.7697   -0.8803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0109   -1.2733   -2.0127 H   0  0  0  0  0  0  0  0  0  0  0  0
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  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 12  3  1  0
 30 12  1  0
 10  6  1  0
 30 17  1  0
 29 25  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  6
  4 35  1  0
  4 36  1  0
 14 41  1  6
 15 42  1  0
 15 43  1  0
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 16 45  1  0
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 17 47  1  1
 18 48  1  0
 18 49  1  0
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 26 62  1  0
 27 63  1  0
 29 64  1  0
 30 65  1  6
  7 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
M  END


  Mrv1652309062221532D          

 30 34  0  0  1  0            999 V2000
    2.2576    0.1410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0242    0.6877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6790    0.2870    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3945    0.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0063    0.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8136    0.3138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1510    1.0667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9713    0.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1409    0.1711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4254   -0.2397    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6689   -0.6086    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8486   -0.5204    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    1.1285   -1.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3219   -1.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0689   -0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6224    0.1735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693    0.9587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9228    1.5705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7294    1.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4449    1.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0566    1.2543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7890    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9824    0.6118    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0421   -0.3469    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
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  5 11  2  0  0  0  0
 12 11  1  1  0  0  0
  3 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
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 17 18  1  0  0  0  0
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M  END
> <DATABASE_ID>
NP0236894

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1CC(=N[C@]11O[C@@H](C)C[C@@H]2CCCCCCCC3=CC=C(N3)[C@@H]12)C1=CC=CN1

> <INCHI_IDENTIFIER>
InChI=1S/C25H35N3O2/c1-17-15-18-9-6-4-3-5-7-10-19-12-13-21(27-19)24(18)25(30-17)23(29-2)16-22(28-25)20-11-8-14-26-20/h8,11-14,17-18,23-24,26-27H,3-7,9-10,15-16H2,1-2H3/t17-,18-,23-,24-,25-/m0/s1

> <INCHI_KEY>
JPTGQNMDWMSVSF-OJDBHETBSA-N

> <FORMULA>
C25H35N3O2

> <MOLECULAR_WEIGHT>
409.574

> <EXACT_MASS>
409.272927379

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
46.64812932446985

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,2'S,3S,5'S,7'S)-3-methoxy-5'-methyl-5-(1H-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0^{2,7}]octadecane]-1'(17'),15'-diene

> <JCHEM_LOGP>
5.3115347239999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.275093217262526

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.655183022458655

> <JCHEM_PKA_STRONGEST_BASIC>
0.6688927804195948

> <JCHEM_POLAR_SURFACE_AREA>
62.4

> <JCHEM_REFRACTIVITY>
119.22980000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,2'S,3S,5'S,7'S)-3-methoxy-5'-methyl-5-(1H-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0^{2,7}]octadecane]-1'(17'),15'-diene

> <JCHEM_VEBER_RULE>
0

$$$$

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       4.214   0.263   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.645   1.284   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.868   0.536   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.203   1.302   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.345   0.269   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.852   0.586   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.482   1.991   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.013   1.827   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.330   0.319   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      11.994  -0.447   0.000  0.00  0.00           N+0
HETATM   11  N   UNK     0       8.715  -1.136   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       7.184  -0.971   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.656  -2.437   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.623  -3.579   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.096  -5.045   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.118  -3.255   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.645  -1.790   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.140  -1.466   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.107  -2.608   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.601  -2.284   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.129  -0.818   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.162   0.324   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.689   1.790   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.723   2.932   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.228   2.608   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.564   3.375   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.706   2.341   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.206   0.818   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       3.701   1.142   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       5.679  -0.648   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   12                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6                                                       
CONECT   11    5   12                                                       
CONECT   12   11    3   13   30                                             
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   30                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28   25                                                       
CONECT   30   28   17   12                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₅N₃O₂

Average Mass

409.5740 Da

Monoisotopic Mass

409.27293 Da

IUPAC Name

(2R,2'S,3S,5'S,7'S)-3-methoxy-5'-methyl-5-(1H-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0^{2,7}]octadecane]-1'(17'),15'-diene

Traditional Name

(2R,2'S,3S,5'S,7'S)-3-methoxy-5'-methyl-5-(1H-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0^{2,7}]octadecane]-1'(17'),15'-diene

CAS Registry Number

Not Available

SMILES

CO[C@H]1CC(=N[C@]11O[C@@H](C)C[C@@H]2CCCCCCCC3=CC=C(N3)[C@@H]12)C1=CC=CN1

InChI Identifier

InChI=1S/C25H35N3O2/c1-17-15-18-9-6-4-3-5-7-10-19-12-13-21(27-19)24(18)25(30-17)23(29-2)16-22(28-25)20-11-8-14-26-20/h8,11-14,17-18,23-24,26-27H,3-7,9-10,15-16H2,1-2H3/t17-,18-,23-,24-,25-/m0/s1

InChI Key

JPTGQNMDWMSVSF-OJDBHETBSA-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
Streptomyces cacaoi	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxanes

Sub Class

Not Available

Direct Parent

Oxanes

Alternative Parents

Substituents

Oxane
Substituted pyrrole
Pyrrole
Pyrroline
Heteroaromatic compound
Ketimine
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Dialkyl ether
Ether
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Imine
Hydrocarbon derivative
Organopnictogen 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	5.31	ChemAxon
pKa (Strongest Acidic)	15.66	ChemAxon
pKa (Strongest Basic)	0.67	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.4 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	119.23 m³·mol⁻¹	ChemAxon
Polarizability	46.65 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

71115947

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162395783

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene (NP0236894)

MOL for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)

3D MOL for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)

3D SDF for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)

3D-SDF for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)

PDB for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)

3D PDB for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)

SMILES for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)

INCHI for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)

Structure for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)

3D Structure for NP0236894 ((2r,2's,3s,5's,7's)-3-methoxy-5'-methyl-5-(1h-pyrrol-2-yl)-3,4-dihydro-4'-oxa-18'-azaspiro[pyrrole-2,3'-tricyclo[13.2.1.0²,⁷]octadecane]-1'(17'),15'-diene)