NP-MRD: Showing NP-Card for (18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate (NP0193702)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 11:13:59 UTC

Updated at

2022-09-04 11:13:59 UTC

NP-MRD ID

NP0193702

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate

Description

Nortrewiasine belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids. (18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate is found in Mallotus nudiflorus. Based on a literature review very few articles have been published on Nortrewiasine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042213142D          

 51 54  0  0  0  0            999 V2000
   -5.7796    5.4466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1151    4.6929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6302    4.0255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9658    3.2718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4808    2.6044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6604    2.6906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3248    3.4443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8097    4.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4742    4.8654    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.5043    3.5306    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9425    2.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3766    2.1224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1355    2.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0492    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3348    1.4194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6203    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6203    2.6569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0942    1.4194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0942    0.5944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8086    1.8319    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8086    2.6569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5231    1.4194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5231    0.5944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2376    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9521    1.4194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2376    2.6569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8029    1.4964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0108    1.2656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3474    0.8085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1709    0.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0260    0.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5358    1.2507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3616   -0.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1821   -0.2378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5176   -0.9915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8532   -1.7452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0327   -1.6589    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2122   -1.5727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7273   -2.2401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8767   -0.8190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3381   -1.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6737   -1.8314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4941   -1.9177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8230   -0.4103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4875    0.3434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9724    1.0108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6369    1.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1218    2.4319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8164    1.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3013    2.5182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0158    2.9307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  7  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 33 40  1  0  0  0  0
 35 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
 44 45  2  0  0  0  0
 46 45  1  4  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
  5 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END

     RDKit          3D

101104  0  0  0  0  0  0  0  0999 V2000
   -2.6605    6.6393    1.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6575    5.9317    0.3601 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9750    4.6867   -0.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2144    4.1205   -0.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5797    2.8623   -0.5520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6425    2.1461   -1.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3645    2.6650   -1.3938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0714    3.9168   -0.8589 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5335    4.6908   -1.0462 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.2538    2.1085   -2.0643 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3902    1.0334   -2.1205 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2608    0.0742   -3.1524 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3626    0.7273   -1.0377 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1452   -0.4912   -1.3452 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5449   -0.2847   -1.3304 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3616   -0.4097   -2.4323 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8520   -0.7254   -3.5284 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7939   -0.1660   -2.2700 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1498    1.0155   -3.1822 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1900    0.1715   -0.9369 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5685    1.3217   -0.3162 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1549   -0.5721   -0.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6596   -1.5783   -0.8212 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5837   -0.2459    1.1633 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4208   -0.2544    2.1450 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3103    1.0435    1.3080 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8021   -1.6784   -0.4682 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0841   -1.5741    0.9951 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5661   -2.8390   -1.0042 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1072   -2.6722   -1.1618 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3699   -3.7481   -0.4450 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2532   -4.6929    0.3348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6936   -3.2419    0.4891 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9741   -2.8428   -0.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8470   -2.1636    0.8223 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4378   -0.8277    0.8796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5637   -2.7398    2.1283 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0617   -3.9149    2.3073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4511   -4.7767    3.3219 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0671   -4.2881    1.3899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3043   -2.3183    0.5888 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5376   -3.6397    0.1933 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2929   -4.3634    1.0695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8900   -1.3590   -0.4000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9194   -0.5604   -0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9251    0.5187    0.8383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1884    1.5829    0.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4361    1.9133    2.1409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0064    2.5578   -0.2376 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7071    3.6990    0.2186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8161    3.9302   -0.5603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9299    6.2069    2.0236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6108    6.7135    0.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3557    7.7174    1.1930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9784    4.7039    0.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8577    1.1055   -1.6889 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1333    0.3146   -4.1045 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8001    0.7000   -0.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0985    1.5777   -0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9086   -0.7665   -2.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3596   -1.0691   -2.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0513    1.5210   -2.8080 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2831    0.6699   -4.2214 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2697    1.7168   -3.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0025    1.9351   -1.0796 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7523    0.9964    0.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2605    2.0301    0.1412 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2641   -1.0743    1.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5863   -0.8175    1.7207 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0713    0.7712    2.3831 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7501   -0.6782    3.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2805    0.8578    1.8118 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5884    1.5073    0.3244 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7795    1.7650    1.9693 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1452   -1.2367    1.1981 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4536   -0.8216    1.5132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9707   -2.5104    1.5447 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9150   -2.5442   -2.2472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1583   -4.3757   -1.2068 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3282   -4.4233    0.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0080   -4.7018    1.4189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1627   -5.7495   -0.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3870   -2.3971    1.1135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4835   -3.7508   -0.6107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7178   -2.1937   -1.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8310   -0.6730    1.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7208   -5.7362    3.0707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8209   -2.2241    1.5817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8839   -4.4695    2.0794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3347   -4.0004    1.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3894   -5.3955    0.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3770   -1.3786   -1.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8823   -0.6735   -0.7153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6574    0.4176    1.6757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1835    2.9859    2.2000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4828    1.3534    2.2076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0708    1.6129    3.0105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6122    2.2323   -1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3810    4.8106   -0.2346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5339    3.0754   -0.5183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5084    3.9750   -1.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
 43 42  1  0
 42 41  1  0
 41 44  1  0
 44 45  2  0
 45 46  1  0
 46 47  2  0
 47 48  1  0
 47 49  1  0
 49 50  1  0
 50 51  1  0
 49  5  1  0
  5  6  2  0
  6  7  1  0
  7 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 14 27  1  0
 27 28  1  1
 27 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  1
 35 37  1  0
 37 38  2  0
 38 39  1  0
 38 40  1  0
  7  8  2  0
  8  9  1  0
  8  3  1  0
  3  2  1  0
  2  1  1  0
  3  4  2  0
 35 41  1  0
  4  5  1  0
 30 27  1  0
 40 33  1  0
 43 89  1  0
 43 90  1  0
 43 91  1  0
 41 88  1  1
 44 92  1  0
 45 93  1  0
 46 94  1  0
 48 95  1  0
 48 96  1  0
 48 97  1  0
 49 98  1  6
 51 99  1  0
 51100  1  0
 51101  1  0
  6 56  1  0
 12 57  1  0
 13 58  1  0
 13 59  1  0
 14 60  1  6
 18 61  1  6
 19 62  1  0
 19 63  1  0
 19 64  1  0
 21 65  1  0
 21 66  1  0
 21 67  1  0
 24 68  1  0
 25 69  1  0
 25 70  1  0
 25 71  1  0
 26 72  1  0
 26 73  1  0
 26 74  1  0
 28 75  1  0
 28 76  1  0
 28 77  1  0
 30 78  1  6
 31 79  1  6
 32 80  1  0
 32 81  1  0
 32 82  1  0
 33 83  1  1
 34 84  1  0
 34 85  1  0
 36 86  1  0
 39 87  1  0
  1 52  1  0
  1 53  1  0
  1 54  1  0
  4 55  1  0
M  END


  Mrv1652309042213142D          

 51 54  0  0  0  0            999 V2000
   -5.7796    5.4466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1151    4.6929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6302    4.0255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9658    3.2718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4808    2.6044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6604    2.6906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3248    3.4443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8097    4.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4742    4.8654    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.5043    3.5306    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9425    2.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3766    2.1224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1355    2.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0492    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3348    1.4194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6203    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6203    2.6569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0942    1.4194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0942    0.5944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8086    1.8319    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8086    2.6569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5231    1.4194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5231    0.5944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2376    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9521    1.4194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2376    2.6569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8029    1.4964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0108    1.2656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3474    0.8085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1709    0.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0260    0.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5358    1.2507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3616   -0.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1821   -0.2378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5176   -0.9915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8532   -1.7452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0327   -1.6589    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2122   -1.5727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7273   -2.2401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8767   -0.8190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3381   -1.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6737   -1.8314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4941   -1.9177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8230   -0.4103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4875    0.3434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9724    1.0108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6369    1.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1218    2.4319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8164    1.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3013    2.5182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0158    2.9307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  7  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 33 40  1  0  0  0  0
 35 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
 44 45  2  0  0  0  0
 46 45  1  4  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
  5 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0193702

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1\C=C\C=C(C)C(OC)C2=CC(N=C(O)CC(OC(=O)C(C)N(C)C(=O)C(C)C)C3(C)OC3C(C)C3CC1(O)N=C(O)O3)=C(Cl)C(OC)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C36H50ClN3O11/c1-18(2)32(42)40(7)21(5)33(43)50-27-16-28(41)38-23-14-22(15-24(46-8)29(23)37)30(48-10)19(3)12-11-13-26(47-9)36(45)17-25(49-34(44)39-36)20(4)31-35(27,6)51-31/h11-15,18,20-21,25-27,30-31,45H,16-17H2,1-10H3,(H,38,41)(H,39,44)/b13-11+,19-12?

> <INCHI_KEY>
PZDXJLHGUHZVRF-AOWAQQDZSA-N

> <FORMULA>
C36H50ClN3O11

> <MOLECULAR_WEIGHT>
736.26

> <EXACT_MASS>
735.3133871

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
75.4981192526754

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(18E)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1^{10,14}.0^{3,5}]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(N,2-dimethylpropanamido)propanoate

> <JCHEM_LOGP>
5.487938993333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.659516514685061

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6005165204253817

> <JCHEM_PKA_STRONGEST_BASIC>
-0.07516475176188231

> <JCHEM_POLAR_SURFACE_AREA>
181.46999999999997

> <JCHEM_REFRACTIVITY>
189.89729999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(18E)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1^{10,14}.0^{3,5}]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(N,2-dimethylpropanamido)propanoate

> <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     -10.789  10.167   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -11.415   8.760   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0     -10.510   7.514   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -11.136   6.107   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.231   4.862   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.699   5.023   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.073   6.429   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.978   7.675   0.000  0.00  0.00           C+0
HETATM    9 Cl   UNK     0      -8.352   9.082   0.000  0.00  0.00          Cl+0
HETATM   10  N   UNK     0      -6.541   6.590   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -5.493   5.271   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -6.303   3.962   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.986   4.951   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.825   3.420   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.492   2.650   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.158   3.420   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.158   4.960   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.176   2.650   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.176   1.110   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       1.509   3.420   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       1.509   4.960   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.843   2.650   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.843   1.110   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.177   3.420   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.511   2.650   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.177   4.960   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.232   2.793   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.754   2.362   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -4.382   1.509   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -5.919   1.415   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.515   1.124   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -8.467   2.335   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -8.142  -0.283   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -9.673  -0.444   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -10.300  -1.851   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0     -10.926  -3.258   0.000  0.00  0.00           O+0
HETATM   37  N   UNK     0      -9.394  -3.097   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0      -7.863  -2.936   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -6.958  -4.182   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -7.236  -1.529   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0     -11.831  -2.012   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0     -12.458  -3.419   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0     -13.989  -3.580   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -12.736  -0.766   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -12.110   0.641   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -13.015   1.887   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -12.389   3.294   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0     -13.294   4.540   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0     -10.857   3.455   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0     -11.762   4.701   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0     -13.096   5.471   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   49                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   14   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   27   31                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   40                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37   41                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   33                                                       
CONECT   41   35   42   44                                                  
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   41   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47    5   50                                                  
CONECT   50   49   51                                                       
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  108    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₅₀ClN₃O₁₁

Average Mass

736.2600 Da

Monoisotopic Mass

735.31339 Da

IUPAC Name

(18E)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1^{10,14}.0^{3,5}]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(N,2-dimethylpropanamido)propanoate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1\C=C\C=C(C)C(OC)C2=CC(N=C(O)CC(OC(=O)C(C)N(C)C(=O)C(C)C)C3(C)OC3C(C)C3CC1(O)N=C(O)O3)=C(Cl)C(OC)=C2

InChI Identifier

InChI=1S/C36H50ClN3O11/c1-18(2)32(42)40(7)21(5)33(43)50-27-16-28(41)38-23-14-22(15-24(46-8)29(23)37)30(48-10)19(3)12-11-13-26(47-9)36(45)17-25(49-34(44)39-36)20(4)31-35(27,6)51-31/h11-15,18,20-21,25-27,30-31,45H,16-17H2,1-10H3,(H,38,41)(H,39,44)/b13-11+,19-12?

InChI Key

PZDXJLHGUHZVRF-AOWAQQDZSA-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
Trewia nudiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acid esters

Alternative Parents

Substituents

Alpha-amino acid ester
Alanine or derivatives
Anisole
Alkyl aryl ether
Benzenoid
Aryl halide
Aryl chloride
Cyclic carboximidic acid
Tertiary carboxylic acid amide
Carboxylic acid ester
Carboxamide group
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Alkanolamine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Carbonyl group
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	5.49	ChemAxon
pKa (Strongest Acidic)	3.6	ChemAxon
pKa (Strongest Basic)	-0.075	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	181.47 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	189.9 m³·mol⁻¹	ChemAxon
Polarizability	75.5 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

54612244

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate (NP0193702)

MOL for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D MOL for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D SDF for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D-SDF for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

PDB for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D PDB for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

SMILES for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

INCHI for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

Structure for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D Structure for NP0193702 ((18e)-11-chloro-8,21,23-trihydroxy-12,15,20-trimethoxy-2,5,16-trimethyl-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-8,10,12,14(26),16,18,22-heptaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)