NP-MRD: Showing NP-Card for (2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid (NP0220046)

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Record Information

Version

1.0

Created at

2022-09-05 21:14:43 UTC

Updated at

2022-09-05 21:14:43 UTC

NP-MRD ID

NP0220046

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid

Description

Aglaxiflorin B belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. (2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid is found in Aglaia laxiflora. Based on a literature review very few articles have been published on Aglaxiflorin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052223142D          

 50 55  0  0  1  0            999 V2000
   -3.9847    3.7591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5115    3.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6896    3.1551    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6177    2.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7615    3.9770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8677    3.2270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5191    3.9747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3946    2.5512    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5727    2.6231    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1478    3.3303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6561    3.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7280    2.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0315    2.0005    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2044    1.2514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9697    1.0042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3251    0.6167    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0451   -0.1593    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7756   -0.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1128   -0.9967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9334   -1.0812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4169   -0.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0797    0.3402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2591    0.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4772   -0.8621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0316   -1.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4100   -2.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0356   -2.9837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8597   -2.9449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3053   -3.6392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9269   -4.3723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2381   -2.2119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925   -1.5176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2961   -0.9624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3065   -0.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0982   -0.5925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2221    0.5823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4691    0.9195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6628    1.7821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2212    2.4327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6432   -0.6558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0673   -1.4416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8919   -1.4653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6344   -2.1439    0.0000 O   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  1  6  0  0  0
  3  5  1  6  0  0  0
  3  6  1  0  0  0  0
  6  7  1  4  0  0  0
  6  8  2  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 14  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
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 24 25  1  6  0  0  0
 25 26  2  0  0  0  0
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 29 30  1  0  0  0  0
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 31 32  2  0  0  0  0
 25 32  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
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 36 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 40 43  2  0  0  0  0
 34 43  1  0  0  0  0
 43 44  1  0  0  0  0
 16 44  1  0  0  0  0
 44 45  1  6  0  0  0
 44 46  1  0  0  0  0
 24 46  1  0  0  0  0
 46 47  1  1  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
M  END

     RDKit          3D

 94 99  0  0  0  0  0  0  0  0999 V2000
    8.4381    0.0311    0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0087   -0.3950    0.6558 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0788   -1.4168   -2.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9041   -0.6027    0.3027 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3267    0.4581    0.7458 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0964    1.7259    1.4611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6301    1.8228    2.7551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4953    2.9641    3.5126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8343    4.0558    3.0366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2944    3.9823    1.7574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4400    2.8228    1.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6070    0.5445   -0.0979 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2017    1.8700   -0.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7062    2.8889   -0.9178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3132    4.1266   -0.9087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4201    4.3559   -0.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3051    2.1213    0.6466 C   0  0  0  0  0  0  0  0  0  0  0  0
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 10 62  1  0
 10 63  1  0
 11 64  1  0
 11 65  1  0
 12 66  1  0
 12 67  1  0
 16 68  1  6
 17 69  1  1
 19 70  1  0
 20 71  1  0
 21 72  1  0
 22 73  1  0
 23 74  1  0
 35 82  1  0
 38 83  1  0
 38 84  1  0
 38 85  1  0
 39 86  1  0
 42 87  1  0
 42 88  1  0
 42 89  1  0
 45 90  1  0
 46 91  1  6
 49 92  1  0
 49 93  1  0
 49 94  1  0
 26 75  1  0
 27 76  1  0
 30 77  1  0
 30 78  1  0
 30 79  1  0
 31 80  1  0
 32 81  1  0
M  END


  Mrv1652309052223142D          

 50 55  0  0  1  0            999 V2000
   -3.9847    3.7591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5115    3.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6896    3.1551    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6177    2.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7615    3.9770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8677    3.2270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5191    3.9747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3946    2.5512    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5727    2.6231    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1478    3.3303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6561    3.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7280    2.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0315    2.0005    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2044    1.2514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9697    1.0042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3251    0.6167    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0451   -0.1593    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7756   -0.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1128   -0.9967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9334   -1.0812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4169   -0.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0797    0.3402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2591    0.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4772   -0.8621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0316   -1.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4100   -2.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0356   -2.9837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8597   -2.9449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3053   -3.6392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9269   -4.3723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2381   -2.2119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925   -1.5176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2961   -0.9624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0943   -0.4879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6380   -0.7218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3065   -0.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0982   -0.5925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510   -0.1563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2221    0.5823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4691    0.9195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6628    1.7821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2212    2.4327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8006    0.4360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1063    0.8817    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0805    1.7650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0098   -0.0689    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6432   -0.6558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0673   -1.4416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8919   -1.4653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6344   -2.1439    0.0000 O   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  1  6  0  0  0
  3  5  1  6  0  0  0
  3  6  1  0  0  0  0
  6  7  1  4  0  0  0
  6  8  2  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 14  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  2  0  0  0  0
 25 32  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 36 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 40 43  2  0  0  0  0
 34 43  1  0  0  0  0
 43 44  1  0  0  0  0
 16 44  1  0  0  0  0
 44 45  1  6  0  0  0
 44 46  1  0  0  0  0
 24 46  1  0  0  0  0
 46 47  1  1  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0220046

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@](C)(O)C(O)=N[C@@H]1CCCN1C(=O)[C@@H]1[C@@H](C2=CC=CC=C2)[C@@]2(OC3=CC(OC)=CC(OC)=C3[C@@]1(O)[C@H]2OC(C)=O)C1=CC=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C38H44N2O10/c1-7-36(3,44)35(43)39-29-14-11-19-40(29)33(42)32-30(23-12-9-8-10-13-23)38(24-15-17-25(46-4)18-16-24)34(49-22(2)41)37(32,45)31-27(48-6)20-26(47-5)21-28(31)50-38/h8-10,12-13,15-18,20-21,29-30,32,34,44-45H,7,11,14,19H2,1-6H3,(H,39,43)/t29-,30+,32-,34+,36+,37-,38-/m0/s1

> <INCHI_KEY>
ZNVMTRFRMHAFBX-REAKOCMFSA-N

> <FORMULA>
C38H44N2O10

> <MOLECULAR_WEIGHT>
688.774

> <EXACT_MASS>
688.299595625

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
72.03429267544479

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-N-[(2S)-1-[(1R,9R,10S,11R,12R)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0^{2,7}]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid

> <JCHEM_LOGP>
3.8809024219999992

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.214331267757169

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.2970464477473747

> <JCHEM_PKA_STRONGEST_BASIC>
0.7123217594398717

> <JCHEM_POLAR_SURFACE_AREA>
156.57999999999998

> <JCHEM_REFRACTIVITY>
181.1507

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-N-[(2S)-1-[(1R,9R,10S,11R,12R)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0^{2,7}]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid

> <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      -7.438   7.017   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.555   5.755   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.021   5.890   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.886   4.355   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.155   7.424   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -3.486   6.024   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.836   7.419   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0      -2.603   4.762   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      -1.069   4.896   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.276   6.216   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.225   5.870   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.359   4.336   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -0.059   3.734   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -0.382   2.336   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.810   1.874   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.607   1.151   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.084  -0.297   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.448  -0.455   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.077  -1.861   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.609  -2.018   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.512  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.882   0.635   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.350   0.793   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.891  -1.609   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.059  -2.905   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.765  -4.274   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.066  -5.570   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.605  -5.497   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -2.437  -6.793   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -1.730  -8.162   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.311  -4.129   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.479  -2.833   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.419  -1.796   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.909  -0.911   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.924  -1.347   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.172  -0.445   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       7.650  -1.106   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       9.055  -0.292   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.015   1.087   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       4.609   1.716   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       4.971   3.327   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       6.013   4.541   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       3.361   0.814   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.065   1.646   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       2.017   3.295   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       1.885  -0.129   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       3.067  -1.224   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       3.859  -2.691   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       5.398  -2.735   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       3.051  -4.002   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   44                                                  
CONECT   17   16   18   24                                                  
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24   17   25   33   46                                             
CONECT   25   24   26   32                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28   32                                                       
CONECT   32   31   25                                                       
CONECT   33   24   34                                                       
CONECT   34   33   35   43                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   39                                                  
CONECT   37   36   38                                                       
CONECT   38   37                                                            
CONECT   39   36   40                                                       
CONECT   40   39   41   43                                                  
CONECT   41   40   42                                                       
CONECT   42   41                                                            
CONECT   43   40   34   44                                                  
CONECT   44   43   16   45   46                                             
CONECT   45   44                                                            
CONECT   46   44   24   47                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₄₄N₂O₁₀

Average Mass

688.7740 Da

Monoisotopic Mass

688.29960 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@@](C)(O)C(O)=N[C@@H]1CCCN1C(=O)[C@@H]1[C@@H](C2=CC=CC=C2)[C@@]2(OC3=CC(OC)=CC(OC)=C3[C@@]1(O)[C@H]2OC(C)=O)C1=CC=C(OC)C=C1

InChI Identifier

InChI=1S/C38H44N2O10/c1-7-36(3,44)35(43)39-29-14-11-19-40(29)33(42)32-30(23-12-9-8-10-13-23)38(24-15-17-25(46-4)18-16-24)34(49-22(2)41)37(32,45)31-27(48-6)20-26(47-5)21-28(31)50-38/h8-10,12-13,15-18,20-21,29-30,32,34,44-45H,7,11,14,19H2,1-6H3,(H,39,43)/t29-,30+,32-,34+,36+,37-,38-/m0/s1

InChI Key

ZNVMTRFRMHAFBX-REAKOCMFSA-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
Aglaia laxiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

7-O-methylated flavonoids

Alternative Parents

Substituents

4p-methoxyflavonoid-skeleton
5-methoxyflavonoid-skeleton
7-methoxyflavonoid-skeleton
Hydroxyflavonoid
4-hydroxyflavonoid
Flavan
Stilbene
Benzopyran
1-benzopyran
Chromane
Phenol ether
N-acylpyrrolidine
Anisole
Phenoxy compound
Methoxybenzene
Alkyl aryl ether
Benzenoid
Fatty amide
N-acyl-amine
Fatty acyl
Monocyclic benzene moiety
Cyclic alcohol
Tertiary carboxylic acid amide
Tertiary alcohol
Pyrrolidine
Carboxylic acid ester
Secondary carboxylic acid amide
Carboxamide group
Oxacycle
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Carbonyl group
Organonitrogen compound
Organic oxide
Alcohol
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

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

24708887

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10652212

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid (NP0220046)

MOL for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)

3D MOL for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)

3D SDF for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)

3D-SDF for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)

PDB for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)

3D PDB for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)

SMILES for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)

INCHI for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)

Structure for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)

3D Structure for NP0220046 ((2r)-n-[(2s)-1-[(1r,9r,10s,11r,12r)-12-(acetyloxy)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-11-carbonyl]pyrrolidin-2-yl]-2-hydroxy-2-methylbutanimidic acid)