NP-MRD: Showing NP-Card for 2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate (NP0207040)

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Record Information

Version

2.0

Created at

2022-09-05 03:29:44 UTC

Updated at

2022-09-05 03:29:44 UTC

NP-MRD ID

NP0207040

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate

Description

2-[(4R,12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]Henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton. 2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate is found in Strychnos henningsii. Based on a literature review very few articles have been published on 2-[(4R,12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]Henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052205292D          

 29 34  0  0  1  0            999 V2000
    4.1325    5.9139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3399    5.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1352    4.8958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7521    4.5365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9596    3.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3718    3.1591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5765    3.3788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5792    2.3607    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3332    2.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0650    2.4081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7608    1.9648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7248    1.1406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9929    0.7597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2972    1.2031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5286    0.9109    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8896    0.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3627   -0.6164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5349   -0.3342    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5609   -0.2018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2418    0.6680    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9273    1.0388    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4717    0.3962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0012    0.3971    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2468    1.7799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6942    2.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8879    2.2232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6877    1.3831    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1187    1.2090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0861    1.7069    0.0000 C   0  0  2  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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  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
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 23 22  1  1  0  0  0
 18 23  1  0  0  0  0
 15 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  1  0  0  0
 24 29  1  0  0  0  0
 29  8  1  6  0  0  0
 15 29  1  0  0  0  0
M  END

     RDKit          3D

 55 60  0  0  0  0  0  0  0  0999 V2000
    6.0798    2.7376    1.4905 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4142    1.5943    0.8200 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1095    0.8755    0.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0703    1.3390    1.0463 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4824    0.2236    0.3728 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    0.0914    0.7187 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6208    0.9244    1.5979 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1358   -0.8294    0.2045 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2730   -1.8358   -0.7900 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4673   -2.2999   -1.3483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3805   -3.2856   -2.3126 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1763   -3.7872   -2.7054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0050   -3.3367   -2.1616 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0491   -2.3371   -1.1806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0054   -1.6620   -0.4197 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0437   -2.5933    0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2949   -1.7435    0.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0481   -0.5463   -0.5223 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3301    0.6586    0.1227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4675    1.8402   -0.1082 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0407    1.3380   -0.3398 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1172    0.5187   -1.6074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8665   -0.7357   -1.2537 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8023    0.4408    0.8490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1207    0.9706    2.0093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6308    2.2797    2.0973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3680    2.7896    1.0401 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7075    3.3454    1.4653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2658   -0.9137    0.6605 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0458    2.9788    0.9853 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4222    3.6454    1.3734 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2793    2.5415    2.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6141    0.4025   -0.7068 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0434   -0.6674    0.7484 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4374   -1.9394   -1.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2991   -3.6558   -2.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1666   -4.5562   -3.4627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9715   -3.7171   -2.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7461   -2.9545    1.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1609   -3.4608   -0.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0988   -2.3236   -0.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -1.5682    1.2834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3832    0.9655   -0.1603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4139    0.5184    1.2414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8438    2.3774   -1.0052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2978    2.1325   -0.3529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1392    0.2620   -2.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7563    1.0957   -2.3169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0640   -1.2745   -2.2092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9873    0.3904    2.9036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7951    3.6853    0.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2683    3.6461    0.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2711    2.6601    2.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4905    4.2924    2.0168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2527   -1.5376    1.5628 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 26  1  0
 26 25  1  0
 25 24  2  0
 24 29  1  0
 29  8  1  0
  8  6  1  0
  6  7  2  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  1
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 20 27  1  0
 21 24  1  0
 15 29  1  0
 23 15  1  0
 14  9  1  0
 23 18  1  0
 28 52  1  0
 28 53  1  0
 28 54  1  0
 27 51  1  6
 25 50  1  0
 29 55  1  1
  5 33  1  0
  5 34  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 16 39  1  0
 16 40  1  0
 17 41  1  0
 17 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  6
 21 46  1  6
 22 47  1  0
 22 48  1  0
 23 49  1  6
M  END


  Mrv1652309052205292D          

 29 34  0  0  1  0            999 V2000
    4.1325    5.9139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3399    5.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1352    4.8958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7521    4.5365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9596    3.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3718    3.1591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5765    3.3788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5792    2.3607    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3332    2.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0650    2.4081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7608    1.9648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7248    1.1406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9929    0.7597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2972    1.2031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5286    0.9109    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8896    0.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3627   -0.6164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5349   -0.3342    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5609   -0.2018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2418    0.6680    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9273    1.0388    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4717    0.3962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0012    0.3971    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2468    1.7799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6942    2.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8879    2.2232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6877    1.3831    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1187    1.2090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0861    1.7069    0.0000 C   0  0  2  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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  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
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 23 22  1  1  0  0  0
 18 23  1  0  0  0  0
 15 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  1  0  0  0
 24 29  1  0  0  0  0
 29  8  1  6  0  0  0
 15 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207040

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1OC=C2[C@@H]3N(C(=O)COC(C)=O)C4=CC=CC=C4[C@@]33CCN4C[C@@H]1[C@@H]2C[C@@H]34

> <INCHI_IDENTIFIER>
InChI=1S/C23H26N2O4/c1-13-16-10-24-8-7-23-18-5-3-4-6-19(18)25(21(27)12-29-14(2)26)22(23)17(11-28-13)15(16)9-20(23)24/h3-6,11,13,15-16,20,22H,7-10,12H2,1-2H3/t13-,15+,16+,20+,22+,23-/m1/s1

> <INCHI_KEY>
WUOOMFMZURUOKX-DNZVMQJPSA-N

> <FORMULA>
C23H26N2O4

> <MOLECULAR_WEIGHT>
394.471

> <EXACT_MASS>
394.189257325

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
42.19461940720785

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(4R,12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0^{4,12}.0^{4,20}.0^{5,10}.0^{13,18}]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate

> <JCHEM_LOGP>
0.7422894723333326

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.51469328010527

> <JCHEM_PKA_STRONGEST_BASIC>
10.218033870281964

> <JCHEM_POLAR_SURFACE_AREA>
59.08000000000001

> <JCHEM_REFRACTIVITY>
106.49920000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-[(4R,12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0^{4,12}.0^{4,20}.0^{5,10}.0^{13,18}]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       7.714  11.039   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.101   9.549   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.586   9.139   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.004   8.468   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.391   6.978   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.294   5.897   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.810   6.307   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       6.681   4.407   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       8.089   3.784   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.455   4.495   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.754   3.668   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.686   2.129   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.320   1.418   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.021   2.246   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.587   1.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.261   0.156   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.277  -1.151   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       4.732  -0.624   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       2.914  -0.377   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.318   1.247   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.598   1.939   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.614   0.740   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.602   0.741   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.194   3.322   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.162   4.500   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.657   4.150   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.284   2.582   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.222   2.257   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.761   3.186   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                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   29                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14   16   23   29                                             
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   27                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22   18   15                                                  
CONECT   24   21   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   20   28                                                  
CONECT   28   27                                                            
CONECT   29   24    8   15                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   68    0
END

View in JSmol

Synonyms

Value	Source
2-[(4R,12R,16R,17S,18S,20S)-16-Methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0,.0,.0,.0,]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetic acid	Generator

Chemical Formula

C₂₃H₂₆N₂O₄

Average Mass

394.4710 Da

Monoisotopic Mass

394.18926 Da

IUPAC Name

2-[(4R,12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0^{4,12}.0^{4,20}.0^{5,10}.0^{13,18}]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate

Traditional Name

2-[(4R,12R,16R,17S,18S,20S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0^{4,12}.0^{4,20}.0^{5,10}.0^{13,18}]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate

CAS Registry Number

Not Available

SMILES

C[C@H]1OC=C2[C@@H]3N(C(=O)COC(C)=O)C4=CC=CC=C4[C@@]33CCN4C[C@@H]1[C@@H]2C[C@@H]34

InChI Identifier

InChI=1S/C23H26N2O4/c1-13-16-10-24-8-7-23-18-5-3-4-6-19(18)25(21(27)12-29-14(2)26)22(23)17(11-28-13)15(16)9-20(23)24/h3-6,11,13,15-16,20,22H,7-10,12H2,1-2H3/t13-,15+,16+,20+,22+,23-/m1/s1

InChI Key

WUOOMFMZURUOKX-DNZVMQJPSA-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
Strychnos henningsii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Strychnos alkaloids

Sub Class

Not Available

Direct Parent

Strychnos alkaloids

Alternative Parents

Substituents

Strychnan skeleton
Akuammicine-skeleton
Stemmadenine-skeleton
Carbazole
Indole or derivatives
Indolizidine
Aralkylamine
Piperidine
N-alkylpyrrolidine
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Tertiary aliphatic amine
Tertiary amine
Carboxamide group
Carboxylic acid ester
Amino acid or derivatives
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Azacycle
Organic oxygen compound
Amine
Organopnictogen compound
Organic oxide
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
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	0.74	ChemAxon
pKa (Strongest Acidic)	15.51	ChemAxon
pKa (Strongest Basic)	10.22	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	59.08 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	106.5 m³·mol⁻¹	ChemAxon
Polarizability	42.19 Å³	ChemAxon
Number of Rings	6	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

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

163191358

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate (NP0207040)

MOL for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)

3D MOL for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)

3D SDF for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)

3D-SDF for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)

PDB for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)

3D PDB for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)

SMILES for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)

INCHI for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)

Structure for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)

3D Structure for NP0207040 (2-[(4r,12r,16r,17s,18s,20s)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.0⁴,¹².0⁴,²⁰.0⁵,¹⁰.0¹³,¹⁸]henicosa-5,7,9,13-tetraen-11-yl]-2-oxoethyl acetate)