NP-MRD: Showing NP-Card for (1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate (NP0241470)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 01:33:33 UTC

Updated at

2022-09-07 01:33:33 UTC

NP-MRD ID

NP0241470

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate

Description

Epoxycytochalasin D, 19,20- belongs to the class of organic compounds known as isoindoles and derivatives. These are polycyclic compounds containing an isoindole moiety, which is structurally characterized by a cyclohexadiene fused to a pyrrole ring. (1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate was first documented in 2021 (PMID: 33585752). Based on a literature review very few articles have been published on Epoxycytochalasin D, 19,20-.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072203332D          

 38 42  0  0  1  0            999 V2000
    1.7282   -2.6333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3278   -1.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5453   -1.3300    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2768   -1.0095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7231   -0.7155    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6565   -1.7852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9290   -2.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6018   -3.1498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4086   -3.4241    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4790   -4.3081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1512   -3.0292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5425   -3.8166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5824   -2.3224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1757   -2.9858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4728   -2.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8030   -1.5105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1901   -0.7819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3656   -0.8110    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5430   -0.4498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2871   -0.0488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1904    0.3042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1919    1.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8673   -0.2242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5013   -0.2656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3978    0.5761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6220    0.9730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1685    0.8390    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    0.1588    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3611    0.4293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8595    0.8751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2906    1.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5235    2.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3254    2.4580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8943    1.8606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6613    1.0691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0999   -0.6294    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0879   -1.4734    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4196   -2.2096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  1  0  0  0
 13 16  1  0  0  0  0
 16 17  1  1  0  0  0
 18 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 30 35  1  0  0  0  0
 36 28  1  6  0  0  0
 24 36  1  0  0  0  0
 36 37  1  0  0  0  0
  2 37  1  0  0  0  0
 37 38  1  6  0  0  0
M  END

     RDKit          3D

 75 79  0  0  0  0  0  0  0  0999 V2000
    1.3013    1.0008    3.8328 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7530    0.5125    2.7549 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2949   -0.5518    2.8962 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1361   -0.2298    3.9317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0005   -0.5023    1.5253 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2186   -1.3049    1.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4049   -0.6904    1.5300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5233    0.7554    1.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6401    1.5091    0.3323 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9208    2.3594    0.2734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6199    0.7060   -0.8927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2973   -0.2854   -0.9982 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7269    1.1483   -2.0289 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8582    2.6080   -2.2943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323    0.4463   -3.1718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3260    0.7939   -1.4976 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3294    0.4031   -2.3562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0724   -0.5473   -1.7104 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6098   -1.4968   -0.7029 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1816   -2.5062   -1.3137 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1667   -3.8200   -1.4533 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7550   -4.7780   -2.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2828   -4.1955   -1.0121 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0474   -1.0501    0.5440 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6001   -2.2565    1.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0773   -3.3495    1.6958 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8636   -2.1929    1.1787 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4059   -1.0063    0.6019 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2759   -1.2474   -0.5842 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8527    0.0036   -1.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2929    0.7192   -2.1727 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8400    1.8860   -2.6562 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9896    2.3589   -2.0825 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5767    1.6721   -1.0438 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0260    0.5090   -0.5659 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2077   -0.1331    0.4024 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1626    1.0035    1.4138 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4642    1.7321    1.5752 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9820    0.6214    4.8252 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0783    1.7804    3.8501 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2297   -1.4874    3.0654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4912   -0.9978    4.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1878    0.5539    1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1759   -2.4101    1.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2967   -1.3448    1.4949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5171    0.9399    2.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8039    1.2330    2.3271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7994    2.2698    0.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7409    1.6409    0.5670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8631    3.2292    0.9358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0737    2.6049   -0.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8260    2.7566   -2.8353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8600    3.2627   -1.4275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0764    2.9120   -3.0199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7940    0.9721   -3.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0161    1.5492   -0.7845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7209   -1.0924   -2.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5341   -2.0775   -0.3766 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7571   -4.3354   -2.1511 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7727   -5.7041   -1.4973 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4322   -5.0316   -3.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2493   -3.8190    2.5086 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0965   -0.5858    1.3899 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1698   -1.8771   -0.3041 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7510   -1.7198   -1.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3843    0.3513   -2.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3838    2.4261   -3.4686 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4764    3.2643   -2.4060 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4848    2.0150   -0.5663 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4720   -0.0348    0.2408 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3012    0.3504   -0.5766 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4145    1.7633    1.1100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1938    1.2570    2.2352 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8935    2.0688    0.6074 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1970    2.7126    2.0825 H   0  0  0  0  0  0  0  0  0  0  0  0
 38 37  1  0
 37 36  1  0
 36 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 33 34  1  0
 34 35  2  0
 28 27  1  0
 27 25  2  0
 25 26  1  0
 24 25  1  1
 24  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 13 15  1  6
 13 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  2  3
  2 37  1  0
 24 36  1  0
 19 24  1  0
 35 30  1  0
 18 16  1  0
 38 73  1  0
 38 74  1  0
 38 75  1  0
 37 72  1  6
 36 71  1  6
 28 63  1  1
 29 64  1  0
 29 65  1  0
 31 66  1  0
 32 67  1  0
 33 68  1  0
 34 69  1  0
 35 70  1  0
 26 62  1  0
  5 43  1  6
  6 44  1  0
  7 45  1  0
  8 46  1  0
  8 47  1  0
  9 48  1  6
 10 49  1  0
 10 50  1  0
 10 51  1  0
 14 52  1  0
 14 53  1  0
 14 54  1  0
 15 55  1  0
 16 56  1  1
 18 57  1  6
 19 58  1  1
 22 59  1  0
 22 60  1  0
 22 61  1  0
  3 41  1  1
  4 42  1  0
  1 39  1  0
  1 40  1  0
M  END


  Mrv1652309072203332D          

 38 42  0  0  1  0            999 V2000
    1.7282   -2.6333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3278   -1.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5453   -1.3300    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2768   -1.0095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7231   -0.7155    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6565   -1.7852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9290   -2.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6018   -3.1498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4086   -3.4241    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4790   -4.3081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1512   -3.0292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5425   -3.8166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5824   -2.3224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1757   -2.9858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4728   -2.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8030   -1.5105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1901   -0.7819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3656   -0.8110    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5430   -0.4498    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2871   -0.0488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1904    0.3042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1919    1.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8673   -0.2242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5013   -0.2656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3978    0.5761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6220    0.9730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1685    0.8390    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    0.1588    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3611    0.4293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8595    0.8751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2906    1.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5235    2.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3254    2.4580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8943    1.8606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6613    1.0691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0999   -0.6294    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0879   -1.4734    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4196   -2.2096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  1  0  0  0
 13 16  1  0  0  0  0
 16 17  1  1  0  0  0
 18 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 30 35  1  0  0  0  0
 36 28  1  6  0  0  0
 24 36  1  0  0  0  0
 36 37  1  0  0  0  0
  2 37  1  0  0  0  0
 37 38  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0241470

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]2[C@H](CC3=CC=CC=C3)N=C(O)[C@@]22[C@@H](\C=C/C[C@H](C)C(=O)[C@](C)(O)[C@@H]3O[C@H]3[C@H]2OC(C)=O)[C@H](O)C1=C

> <INCHI_IDENTIFIER>
InChI=1S/C30H37NO7/c1-15-10-9-13-20-23(33)17(3)16(2)22-21(14-19-11-7-6-8-12-19)31-28(35)30(20,22)27(37-18(4)32)24-26(38-24)29(5,36)25(15)34/h6-9,11-13,15-16,20-24,26-27,33,36H,3,10,14H2,1-2,4-5H3,(H,31,35)/b13-9-/t15-,16+,20-,21-,22-,23+,24+,26+,27+,29-,30-/m0/s1

> <INCHI_KEY>
WHJRAYUHVRYTTH-XGPNHLKASA-N

> <FORMULA>
C30H37NO7

> <MOLECULAR_WEIGHT>
523.626

> <EXACT_MASS>
523.257002535

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
55.21234934756184

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3S,5R,6R,8S,10Z,12R,13S,15S,16R,17S)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0^{1,16}.0^{3,5}]nonadeca-10,18-dien-2-yl acetate

> <JCHEM_LOGP>
2.470481992004194

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.23083550705477

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.0969472893501737

> <JCHEM_PKA_STRONGEST_BASIC>
5.472023718654161

> <JCHEM_POLAR_SURFACE_AREA>
128.95000000000002

> <JCHEM_REFRACTIVITY>
140.14080000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,5R,6R,8S,10Z,12R,13S,15S,16R,17S)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0^{1,16}.0^{3,5}]nonadeca-10,18-dien-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       3.226  -4.915   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.479  -3.347   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.018  -2.483   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.517  -1.884   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.350  -1.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.226  -3.332   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.734  -4.889   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.990  -5.880   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.496  -6.392   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.627  -8.042   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.882  -5.655   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.613  -7.124   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.687  -4.335   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.795  -5.574   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.349  -4.176   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.099  -2.820   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.821  -1.460   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.282  -1.514   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.747  -0.840   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.136  -0.091   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.822   0.568   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.825   2.244   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.086  -0.418   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.802  -0.496   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.609   1.075   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.161   1.816   0.000  0.00  0.00           O+0
HETATM   27  N   UNK     0       4.048   1.566   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       4.896   0.296   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.274   0.801   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.204   1.634   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.142   2.749   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.577   4.226   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.074   4.588   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.136   3.473   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.701   1.996   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.920  -1.175   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.897  -2.750   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.517  -4.125   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   37                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   24                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13   17   18                                                  
CONECT   17   16   18                                                       
CONECT   18   17   16   19                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19    5   25   36                                             
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   36                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   30                                                       
CONECT   36   28   24   37                                                  
CONECT   37   36    2   38                                                  
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₇NO₇

Average Mass

523.6260 Da

Monoisotopic Mass

523.25700 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]2[C@H](CC3=CC=CC=C3)N=C(O)[C@@]22[C@@H](\C=C/C[C@H](C)C(=O)[C@](C)(O)[C@@H]3O[C@H]3[C@H]2OC(C)=O)[C@H](O)C1=C

InChI Identifier

InChI=1S/C30H37NO7/c1-15-10-9-13-20-23(33)17(3)16(2)22-21(14-19-11-7-6-8-12-19)31-28(35)30(20,22)27(37-18(4)32)24-26(38-24)29(5,36)25(15)34/h6-9,11-13,15-16,20-24,26-27,33,36H,3,10,14H2,1-2,4-5H3,(H,31,35)/b13-9-/t15-,16+,20-,21-,22-,23+,24+,26+,27+,29-,30-/m0/s1

InChI Key

WHJRAYUHVRYTTH-XGPNHLKASA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoindoles and derivatives. These are polycyclic compounds containing an isoindole moiety, which is structurally characterized by a cyclohexadiene fused to a pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Not Available

Direct Parent

Isoindoles and derivatives

Alternative Parents

Substituents

Isoindole or derivatives
Benzenoid
Monocyclic benzene moiety
Acyloin
Cyclic carboximidic acid
Tertiary alcohol
Pyrroline
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source

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

62995571

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131875473

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kushwaha M, Qayum A, Jain SK, Singh J, Srivastava AK, Srivastava S, Sharma N, Abrol V, Malik R, Singh SK, Vishwakarma RA, Jaglan S: Tandem MS-Based Metabolite Profiling of 19,20-Epoxycytochalasin C Reveals the Importance of a Hydroxy Group at the C7 Position for Biological Activity. ACS Omega. 2021 Jan 25;6(5):3717-3726. doi: 10.1021/acsomega.0c05307. eCollection 2021 Feb 9. [PubMed:33585752 ]
LOTUS database [Link]

Showing NP-Card for (1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate (NP0241470)

MOL for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)

3D MOL for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)

3D SDF for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)

3D-SDF for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)

PDB for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)

3D PDB for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)

SMILES for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)

INCHI for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)

Structure for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)

3D Structure for NP0241470 ((1r,2s,3s,5r,6r,8s,10z,12r,13s,15s,16r,17s)-17-benzyl-6,13,19-trihydroxy-6,8,15-trimethyl-14-methylidene-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,18-dien-2-yl acetate)