NP-MRD: Showing NP-Card for (10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one (NP0188104)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 04:22:48 UTC

Updated at

2022-09-04 04:22:48 UTC

NP-MRD ID

NP0188104

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one

Description

(5R)-5,8,8abeta,9-Tetrahydro-9beta-hydroxy-10-methoxy-5-(3,5-dimethoxy-4-hydroxyphenyl)furo[3',4':6,7]Naphtho[2,3-d]-1,3-dioxol-6(5aalphaH)-one belongs to the class of organic compounds known as podophyllotoxins. These are tetralin lignans in which the benzene moiety of the tetralin skeleton is fused to a 1,3-dioxolane and the cyclohexane is fused to a butyrolactone (pyrrolidin-2-one). (10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one is found in Linum flavum. Based on a literature review very few articles have been published on (5R)-5,8,8abeta,9-Tetrahydro-9beta-hydroxy-10-methoxy-5-(3,5-dimethoxy-4-hydroxyphenyl)furo[3',4':6,7]Naphtho[2,3-d]-1,3-dioxol-6(5aalphaH)-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042206222D          

 31 35  0  0  1  0            999 V2000
    4.7812    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -2.7604    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8532   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5983   -0.4834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2803   -2.6029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7652   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2803   -1.2680    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    2.1896    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  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  2  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 22 20  1  6  0  0  0
  6 22  1  0  0  0  0
 17 22  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  9 25  1  0  0  0  0
  5 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  2  0  0  0  0
  3 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 53 57  0  0  0  0  0  0  0  0999 V2000
   -4.5698   -1.9080    2.3855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7058   -0.7903    1.5425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7319   -0.3430    0.6844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5203   -0.9527    0.5684 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5104   -0.5354   -0.2834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2433   -1.2834   -0.3113 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7613   -0.7328    0.6409 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3561   -0.3279    1.8888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2343    0.1922    2.8188 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5691    0.3184    2.5043 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9686   -0.0966    1.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3477    0.0583    0.9659 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7800    1.2936    0.4198 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0860   -0.6117    0.3186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5877   -1.0490   -1.0318 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8344   -0.5934   -1.3355 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4973   -0.6145   -1.9715 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7084   -0.9789   -3.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3489   -0.9775   -3.8697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5102   -1.3158   -2.8200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7559   -1.3785   -2.9974 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3197   -1.5382   -1.6537 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2280    0.8623    3.6018 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2445    1.4972    4.4331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1105    0.6733    4.1301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7949    0.5767   -1.0466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0141    1.2362   -0.9674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2961    2.3547   -1.7372 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3231    2.8396   -2.6255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9751    0.7630   -0.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2142    1.4021    0.0112 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1611   -2.7650    1.7849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8839   -1.7334    3.2402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5544   -2.1609    2.8213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3460   -1.8318    1.1974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4636   -2.3104    0.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828   -0.3950    2.2142 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1518    1.9803    1.2232 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9841    1.8503   -0.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6288    1.1870   -0.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5463   -2.1776   -0.9821 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4962   -1.2872   -1.0916 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2866    0.4375   -1.7930 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3106   -0.2183   -3.9132 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0931   -1.9958   -3.4617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7586   -2.5732   -1.7488 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5783    1.3532    5.4809 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0795    2.5354    4.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0470    0.9378   -1.7179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2440    2.1374   -3.4726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5993    3.8571   -3.0079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3264    2.9204   -2.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4224    2.2121   -0.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5 26  2  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 27 30  2  0
 30 31  1  0
  5  6  1  0
  6 22  1  0
 22 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 17 15  1  0
 15 16  1  0
 15 14  1  0
 14 11  2  0
 11 12  1  0
 12 13  1  0
 11 10  1  0
 10  9  2  0
  9 25  1  0
 25 24  1  0
 24 23  1  0
  9  8  1  0
  8  7  2  0
 30  3  1  0
  7  6  1  0
 20 22  1  0
  7 14  1  0
 23 10  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
 26 49  1  0
 29 50  1  0
 29 51  1  0
 29 52  1  0
 31 53  1  0
  6 36  1  1
 22 46  1  1
 17 43  1  6
 18 44  1  0
 18 45  1  0
 15 41  1  1
 16 42  1  0
 13 38  1  0
 13 39  1  0
 13 40  1  0
 24 47  1  0
 24 48  1  0
  8 37  1  0
M  END


  Mrv1652309042206222D          

 31 35  0  0  1  0            999 V2000
    4.7812    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -2.7604    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8532   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5983   -0.4834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2803   -2.6029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7652   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2803   -1.2680    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    2.1896    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  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  2  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 22 20  1  6  0  0  0
  6 22  1  0  0  0  0
 17 22  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  9 25  1  0  0  0  0
  5 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  2  0  0  0  0
  3 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0188104

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1O)[C@H]1[C@@H]2[C@H](COC2=O)[C@@H](O)C2=C(OC)C3=C(OCO3)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H22O9/c1-26-12-4-9(5-13(27-2)19(12)24)15-10-6-14-20(31-8-30-14)21(28-3)17(10)18(23)11-7-29-22(25)16(11)15/h4-6,11,15-16,18,23-24H,7-8H2,1-3H3/t11-,15+,16-,18+/m0/s1

> <INCHI_KEY>
HCKCVXCPSCVJQG-QOQPWIFLSA-N

> <FORMULA>
C22H22O9

> <MOLECULAR_WEIGHT>
430.409

> <EXACT_MASS>
430.126382288

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
42.70026641044069

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(10R,11R,15R,16R)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0^{3,7}.0^{11,15}]hexadeca-1,3(7),8-trien-12-one

> <JCHEM_LOGP>
1.3192329476666673

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.794563193168795

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.330425634892501

> <JCHEM_PKA_STRONGEST_BASIC>
-3.326064604663591

> <JCHEM_POLAR_SURFACE_AREA>
112.91000000000003

> <JCHEM_REFRACTIVITY>
105.8859

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(10R,11R,15R,16R)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0^{3,7}.0^{11,15}]hexadeca-1,3(7),8-trien-12-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       8.925   4.087   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.925   2.547   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.591   1.777   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.591   0.237   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.591  -2.843   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.925  -2.073   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.259  -2.843   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.259  -4.383   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.925  -5.153   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.925  -6.693   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.259  -7.463   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.591  -4.383   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.258  -5.153   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.258  -6.693   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.924  -4.383   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.459  -4.859   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.554  -3.613   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.459  -2.367   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.983  -0.902   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.723  -4.859   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      12.628  -3.613   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.723  -2.367   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.924   1.777   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.590   2.547   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.590   4.087   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.258   2.547   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.258   4.087   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   30                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   26                                                  
CONECT    6    5    7   22                                                  
CONECT    7    6    8   14                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   25                                                  
CONECT   10    9   11   23                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11    7   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    6   17                                                  
CONECT   23   10   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    9                                                       
CONECT   26    5   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27    3   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Value	Source
(5R)-5,8,8Abeta,9-tetrahydro-9b-hydroxy-10-methoxy-5-(3,5-dimethoxy-4-hydroxyphenyl)furo[3',4':6,7]naphtho[2,3-D]-1,3-dioxol-6(5aalphah)-one	Generator
(5R)-5,8,8Abeta,9-tetrahydro-9β-hydroxy-10-methoxy-5-(3,5-dimethoxy-4-hydroxyphenyl)furo[3',4':6,7]naphtho[2,3-D]-1,3-dioxol-6(5aalphah)-one	Generator

Chemical Formula

C₂₂H₂₂O₉

Average Mass

430.4090 Da

Monoisotopic Mass

430.12638 Da

IUPAC Name

(10R,11R,15R,16R)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0^{3,7}.0^{11,15}]hexadeca-1,3(7),8-trien-12-one

Traditional Name

(10R,11R,15R,16R)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0^{3,7}.0^{11,15}]hexadeca-1,3(7),8-trien-12-one

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(OC)=C1O)[C@H]1[C@@H]2[C@H](COC2=O)[C@@H](O)C2=C(OC)C3=C(OCO3)C=C12

InChI Identifier

InChI=1S/C22H22O9/c1-26-12-4-9(5-13(27-2)19(12)24)15-10-6-14-20(31-8-30-14)21(28-3)17(10)18(23)11-7-29-22(25)16(11)15/h4-6,11,15-16,18,23-24H,7-8H2,1-3H3/t11-,15+,16-,18+/m0/s1

InChI Key

HCKCVXCPSCVJQG-QOQPWIFLSA-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
Linum flavum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as podophyllotoxins. These are tetralin lignans in which the benzene moiety of the tetralin skeleton is fused to a 1,3-dioxolane and the cyclohexane is fused to a butyrolactone (pyrrolidin-2-one).

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Lignan lactones

Sub Class

Podophyllotoxins

Direct Parent

Podophyllotoxins

Alternative Parents

Substituents

Podophyllotoxin
1-aryltetralin lignan
Linear furanonaphthodioxole
Naphthofuran
Methoxyphenol
M-dimethoxybenzene
Dimethoxybenzene
Tetralin
Benzodioxole
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Phenol
Benzenoid
Gamma butyrolactone
Monocyclic benzene moiety
Tetrahydrofuran
Lactone
Carboxylic acid ester
Secondary alcohol
Acetal
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Ether
Monocarboxylic acid or derivatives
Alcohol
Carbonyl group
Organic oxygen compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.32	ChemAxon
pKa (Strongest Acidic)	9.33	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	112.91 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	105.89 m³·mol⁻¹	ChemAxon
Polarizability	42.7 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

15108761

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one (NP0188104)

MOL for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)

3D MOL for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)

3D SDF for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)

3D-SDF for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)

PDB for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)

3D PDB for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)

SMILES for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)

INCHI for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)

Structure for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)

3D Structure for NP0188104 ((10r,11r,15r,16r)-16-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-2-methoxy-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one)