NP-MRD: Showing NP-Card for (9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one (NP0186601)

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Record Information

Version

2.0

Created at

2022-09-04 02:30:54 UTC

Updated at

2022-09-04 02:30:55 UTC

NP-MRD ID

NP0186601

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one

Description

(AlphaS)-alpha-Methyl-1,7beta-tetramethylene-2-[(2S)-4alpha-methyl-5-oxotetrahydrofuran-2alpha-yl]-5beta-hydroxy-6alpha-ethyl-4,5,6,7-tetrahydro-1H-indole-4beta-acetic acid lactone belongs to the class of organic compounds known as stichoneurine-type alkaloids. These are stemona alkaloids with a structure that typically contains a 3-methyloxolan-2-one and a 5-propyloxolan-2-one moieties that are attached to the characteristic pyrrolo[1,2-a]azepine skeleton at the C3 and C9 position, respectively. (9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one is found in Stemona tuberosa. Based on a literature review very few articles have been published on (alphaS)-alpha-Methyl-1,7beta-tetramethylene-2-[(2S)-4alpha-methyl-5-oxotetrahydrofuran-2alpha-yl]-5beta-hydroxy-6alpha-ethyl-4,5,6,7-tetrahydro-1H-indole-4beta-acetic acid lactone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042204302D          

 27 31  0  0  1  0            999 V2000
    4.0829    3.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3558    2.9223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3298    2.0977    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0367    1.6724    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8258    1.9131    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2986    1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1235    1.2221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8017    0.5784    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0424   -0.2107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0218    0.8475    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3000    0.4480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1139   -0.3558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2920   -0.4272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8667   -1.1341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1886   -1.8937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5656   -2.4345    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6370   -3.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8587   -2.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0991   -2.3311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0448   -1.2055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9701    0.3325    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5931    0.8733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5586    1.6976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8927    2.1846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0968    1.9676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7702    1.2100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589    0.4823    0.0000 C   0  0  0  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  6  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  1  0  0  0
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 14 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  2  0  0  0  0
 23 22  1  6  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 21 27  1  0  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
   -4.6766   -1.4704    0.5715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1068   -0.9628   -0.7074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7430   -0.3385   -0.5474 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8741    0.8240    0.4102 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7422    1.7617   -0.2128 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9210    2.5859   -0.9662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1182    3.0663   -2.1355 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7139    2.8240   -0.1355 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0061    4.0170    0.7537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5967    1.5486    0.6700 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4034    0.7820    0.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9122    1.1929    0.1430 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6599    0.1263   -0.2554 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1115    0.1234   -0.5090 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9265    0.2988    0.7600 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3058    0.6024    0.1638 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0961    1.5135    1.0573 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9289    1.2642   -1.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7794    1.7648   -1.9165 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5363    1.2437   -1.2696 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8441   -0.9345   -0.3800 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3998   -0.5356   -0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7052   -1.2674   -0.0204 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5661   -2.5197   -0.8253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7923   -3.5900   -0.1330 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6033   -3.2178    0.2408 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2075   -2.2785   -0.7809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6084   -0.9371    0.8497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9963   -1.3937    1.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9517   -2.5432    0.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1457   -1.7293   -1.5103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7745   -0.1340   -1.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4458    0.0733   -1.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3620    0.5436    1.3652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8330    2.9952   -0.7864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4618    4.9026    0.3494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6314    3.8527    1.7860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0979    4.2130    0.8325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5217    1.7832    1.7719 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2829    2.1875    0.3285 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4736   -0.7773   -1.0152 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5169    1.1814    1.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9433   -0.6063    1.3712 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8373   -0.3576    0.0078 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1459    1.4967    0.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7456    2.5582    0.9636 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0721    1.1292    2.0850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8788   -1.5054    1.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1487   -2.2397   -1.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5795   -2.9443   -1.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7367   -4.4652   -0.8294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3512   -3.8791    0.7810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2206   -4.1255    0.3555 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5712   -2.7138    1.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8676   -2.5438   -1.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3018   -2.4457   -0.7552 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  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 21  1  0
 21 13  1  0
 13 12  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 18 20  1  0
 23  3  1  0
 20 14  1  0
 10  4  1  0
 12 11  1  0
 21 22  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  6
  4 34  1  1
  8 35  1  6
  9 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  1
 23 48  1  1
 24 49  1  0
 24 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  0
 26 54  1  0
 27 55  1  0
 27 56  1  0
 12 40  1  0
 14 41  1  6
 15 42  1  0
 15 43  1  0
 16 44  1  6
 17 45  1  0
 17 46  1  0
 17 47  1  0
M  END


  Mrv1652309042204302D          

 27 31  0  0  1  0            999 V2000
    4.0829    3.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3558    2.9223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3298    2.0977    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0367    1.6724    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8258    1.9131    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2986    1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1235    1.2221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8017    0.5784    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0424   -0.2107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0218    0.8475    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3000    0.4480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1139   -0.3558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2920   -0.4272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8667   -1.1341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1886   -1.8937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5656   -2.4345    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6370   -3.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8587   -2.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0991   -2.3311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0448   -1.2055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9701    0.3325    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5931    0.8733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5586    1.6976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8927    2.1846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0968    1.9676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7702    1.2100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589    0.4823    0.0000 C   0  0  0  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  6  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  1  0  0  0
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 14 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  2  0  0  0  0
 23 22  1  6  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 21 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0186601

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1[C@@H]2OC(=O)[C@@H](C)[C@@H]2C2=C3[C@@H]1CCCCN3C(=C2)[C@@H]1C[C@H](C)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C22H29NO4/c1-4-13-14-7-5-6-8-23-16(17-9-11(2)21(24)26-17)10-15(19(14)23)18-12(3)22(25)27-20(13)18/h10-14,17-18,20H,4-9H2,1-3H3/t11-,12-,13+,14+,17-,18+,20-/m0/s1

> <INCHI_KEY>
RFGMIDHPFYCJDM-CONZVTBHSA-N

> <FORMULA>
C22H29NO4

> <MOLECULAR_WEIGHT>
371.477

> <EXACT_MASS>
371.209658418

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
41.1956853969905

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9R,10R,11S,14S,15R)-10-ethyl-14-methyl-3-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0^{4,16}.0^{11,15}]hexadeca-1(16),2-dien-13-one

> <JCHEM_LOGP>
3.8168443099999996

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.789266330584965

> <JCHEM_POLAR_SURFACE_AREA>
57.53000000000001

> <JCHEM_REFRACTIVITY>
100.7165

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(9R,10R,11S,14S,15R)-10-ethyl-14-methyl-3-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0^{4,16}.0^{11,15}]hexadeca-1(16),2-dien-13-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       7.621   6.183   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.264   5.455   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.216   3.916   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.535   3.122   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.008   3.571   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.891   2.309   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.430   2.281   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.963   1.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.413  -0.393   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.507   1.582   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.160   0.836   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.813  -0.664   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.278  -0.797   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.484  -2.117   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.085  -3.535   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.922  -4.544   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.056  -6.079   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.603  -3.751   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.185  -4.351   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       1.950  -2.250   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0       3.678   0.621   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       4.840   1.630   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.776   3.169   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.533   4.078   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.047   3.673   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.438   2.259   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.163   0.900   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    4   11                                                  
CONECT   11   10   12   22                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   14                                                       
CONECT   21   13   22   27                                                  
CONECT   22   21   11   23                                                  
CONECT   23   22    3   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   21                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Value	Source
(AlphaS)-a-methyl-1,7b-tetramethylene-2-[(2S)-4a-methyl-5-oxotetrahydrofuran-2a-yl]-5b-hydroxy-6a-ethyl-4,5,6,7-tetrahydro-1H-indole-4b-acetate lactone	Generator
(AlphaS)-a-methyl-1,7b-tetramethylene-2-[(2S)-4a-methyl-5-oxotetrahydrofuran-2a-yl]-5b-hydroxy-6a-ethyl-4,5,6,7-tetrahydro-1H-indole-4b-acetic acid lactone	Generator
(AlphaS)-alpha-methyl-1,7beta-tetramethylene-2-[(2S)-4alpha-methyl-5-oxotetrahydrofuran-2alpha-yl]-5beta-hydroxy-6alpha-ethyl-4,5,6,7-tetrahydro-1H-indole-4beta-acetate lactone	Generator
(AlphaS)-α-methyl-1,7β-tetramethylene-2-[(2S)-4α-methyl-5-oxotetrahydrofuran-2α-yl]-5β-hydroxy-6α-ethyl-4,5,6,7-tetrahydro-1H-indole-4β-acetate lactone	Generator
(AlphaS)-α-methyl-1,7β-tetramethylene-2-[(2S)-4α-methyl-5-oxotetrahydrofuran-2α-yl]-5β-hydroxy-6α-ethyl-4,5,6,7-tetrahydro-1H-indole-4β-acetic acid lactone	Generator

Chemical Formula

C₂₂H₂₉NO₄

Average Mass

371.4770 Da

Monoisotopic Mass

371.20966 Da

IUPAC Name

(9R,10R,11S,14S,15R)-10-ethyl-14-methyl-3-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0^{4,16}.0^{11,15}]hexadeca-1(16),2-dien-13-one

Traditional Name

(9R,10R,11S,14S,15R)-10-ethyl-14-methyl-3-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0^{4,16}.0^{11,15}]hexadeca-1(16),2-dien-13-one

CAS Registry Number

Not Available

SMILES

CC[C@H]1[C@@H]2OC(=O)[C@@H](C)[C@@H]2C2=C3[C@@H]1CCCCN3C(=C2)[C@@H]1C[C@H](C)C(=O)O1

InChI Identifier

InChI=1S/C22H29NO4/c1-4-13-14-7-5-6-8-23-16(17-9-11(2)21(24)26-17)10-15(19(14)23)18-12(3)22(25)27-20(13)18/h10-14,17-18,20H,4-9H2,1-3H3/t11-,12-,13+,14+,17-,18+,20-/m0/s1

InChI Key

RFGMIDHPFYCJDM-CONZVTBHSA-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
Stemona tuberosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stichoneurine-type alkaloids. These are stemona alkaloids with a structure that typically contains a 3-methyloxolan-2-one and a 5-propyloxolan-2-one moieties that are attached to the characteristic pyrrolo[1,2-a]azepine skeleton at the C3 and C9 position, respectively.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Stemona alkaloids

Sub Class

Stemoamide-type alkaloids

Direct Parent

Stichoneurine-type alkaloids

Alternative Parents

Substituents

Stichoneurine-type alkaloid
Pyrroloazepine
Indole or derivatives
Azepine
Dicarboxylic acid or derivatives
Gamma butyrolactone
Substituted pyrrole
Heteroaromatic compound
Tetrahydrofuran
Pyrrole
Carboxylic acid ester
Lactone
Azacycle
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organopnictogen compound
Carbonyl group
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.82	ChemAxon
pKa (Strongest Basic)	-6.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	100.72 m³·mol⁻¹	ChemAxon
Polarizability	41.2 Å³	ChemAxon
Number of Rings	5	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

62937531

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12166273

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one (NP0186601)

MOL for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)

3D MOL for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)

3D SDF for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)

3D-SDF for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)

PDB for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)

3D PDB for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)

SMILES for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)

INCHI for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)

Structure for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)

3D Structure for NP0186601 ((9r,10r,11s,14s,15r)-10-ethyl-14-methyl-3-[(2s,4s)-4-methyl-5-oxooxolan-2-yl]-12-oxa-4-azatetracyclo[7.6.1.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(16),2-dien-13-one)