NP-MRD: Showing NP-Card for (9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene (NP0153460)

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Record Information

Version

2.0

Created at

2022-09-02 10:07:12 UTC

Updated at

2022-09-02 10:07:12 UTC

NP-MRD ID

NP0153460

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene

Description

(9S,10R)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]Nonadeca-1(19),2,4,6,12,14(18)-hexaene, also known as rubschisandrin, belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. (9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene is found in Kadsura coccinea, Kadsura interior, Schisandra chinensis and Schisandra lancifolia. Based on a literature review very few articles have been published on (9S,10R)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]Nonadeca-1(19),2,4,6,12,14(18)-hexaene.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022212072D          

 29 32  0  0  1  0            999 V2000
    4.6670    2.0963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8637    1.8108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0393    2.1129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0429    2.9379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3302    3.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6140    2.9442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6104    2.1192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0499    1.2268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9738    0.2997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3230    1.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5602    0.8155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0979    0.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8180    3.1612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4087    3.8775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4163    3.8811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8320    3.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4226    2.4522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4024    2.4485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7674    1.6730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2743    0.8446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9773    1.8415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7295    2.1803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6397    3.0004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6257    4.6734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3419    5.0828    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2210    5.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1379    4.8658    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6731    5.5381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5473    4.1495    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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
   -2.7897   -4.5652    0.5886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9905   -3.2863    0.0768 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0222   -2.2965    0.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7323   -2.5131    0.5084 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1878   -1.5317    0.4540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1863   -0.2774   -0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4409   -0.0316   -0.5828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6873    1.2058   -1.1236 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5147    1.5154   -2.4947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3535   -1.0559   -0.5082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6703   -0.8897   -0.9777 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7066   -0.4243   -0.1531 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4993    1.0015   -0.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7520    1.3563   -0.7610 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0686    2.6815   -0.8254 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1618    3.6227   -0.3816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0792    3.2268    0.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4231    1.9046    0.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5967    1.4312    0.7293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7948    1.1240    2.1007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7754    4.3792    0.5015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0108    5.5078    0.1226 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2334    5.0032   -0.3402 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8961    0.5420   -1.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2562   -0.5089   -0.1463 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2626    0.1551    1.2081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4546   -1.7455   -0.2177 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3349   -3.0030   -0.2886 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5056   -1.9972    0.9509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4004   -5.2587   -0.1837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1117   -4.5364    1.4569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7958   -4.9429    0.9290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4540   -3.4714    0.9284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7816    2.3267   -2.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1129    0.6389   -3.0277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5127    1.7965   -2.8946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3349   -0.4676    0.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6540   -0.9945   -0.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9451    0.6331   -0.4291 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0336    2.9532   -1.2279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2635    0.1350    2.1571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5911    1.8359    2.4694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8611    1.2313    2.6553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0968    6.1486    1.0111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5428    6.0286   -0.7045 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7501    1.2055   -1.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -0.0188   -2.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3208   -0.7699   -0.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2758    0.5753    1.4832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9614    1.0150    1.1425 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6637   -0.5411    1.9459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9076   -1.7462   -1.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7165   -3.8314   -0.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1723   -2.7338   -0.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7136   -3.2110    0.7313 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4160   -3.0625    1.1911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8287   -1.4683    1.8593 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  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  2  0
 10 11  1  0
 11 12  1  0
  6 13  1  0
 13 14  2  0
 14 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 14 15  1  0
 15 16  2  0
 16 23  1  0
 23 22  1  0
 22 21  1  0
 21 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 10  3  1  0
 18 13  1  0
 29  5  1  0
 17 16  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  9 34  1  0
  9 35  1  0
  9 36  1  0
 12 37  1  0
 12 38  1  0
 12 39  1  0
 24 46  1  0
 24 47  1  0
 25 48  1  6
 26 49  1  0
 26 50  1  0
 26 51  1  0
 27 52  1  6
 28 53  1  0
 28 54  1  0
 28 55  1  0
 29 56  1  0
 29 57  1  0
 15 40  1  0
 22 44  1  0
 22 45  1  0
 20 41  1  0
 20 42  1  0
 20 43  1  0
M  END


  Mrv1652309022212072D          

 29 32  0  0  1  0            999 V2000
    4.6670    2.0963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8637    1.8108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0393    2.1129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0429    2.9379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3302    3.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6140    2.9442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6104    2.1192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0499    1.2268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9738    0.2997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3230    1.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5602    0.8155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0979    0.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8180    3.1612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4087    3.8775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4163    3.8811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8320    3.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4226    2.4522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4024    2.4485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7674    1.6730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2743    0.8446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9773    1.8415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7295    2.1803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6397    3.0004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6257    4.6734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3419    5.0828    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2210    5.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1379    4.8658    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6731    5.5381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5473    4.1495    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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0153460

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C(OC)=C1OC)C1=C(C[C@@H](C)[C@@H](C)C2)C=C2OCOC2=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C23H28O6/c1-12-7-14-9-16(24-3)20(25-4)22(26-5)18(14)19-15(8-13(12)2)10-17-21(23(19)27-6)29-11-28-17/h9-10,12-13H,7-8,11H2,1-6H3/t12-,13+/m0/s1

> <INCHI_KEY>
RTZKSTLPRTWFEV-QWHCGFSZSA-N

> <FORMULA>
C23H28O6

> <MOLECULAR_WEIGHT>
400.471

> <EXACT_MASS>
400.188588622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
43.33505236216409

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9S,10R)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0^{2,7}.0^{14,18}]nonadeca-1(19),2(7),3,5,12,14(18)-hexaene

> <ALOGPS_LOGP>
4.37

> <JCHEM_LOGP>
4.639311981666667

> <ALOGPS_LOGS>
-4.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.196413763613773

> <JCHEM_POLAR_SURFACE_AREA>
55.38000000000001

> <JCHEM_REFRACTIVITY>
109.39329999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.62e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(9S,10R)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0^{2,7}.0^{14,18}]nonadeca-1(19),2(7),3,5,12,14(18)-hexaene

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       8.712   3.913   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.212   3.380   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.673   3.944   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.680   5.484   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.350   6.260   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.013   5.496   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.006   3.956   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.960   2.290   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.818   0.559   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.336   3.180   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.779   1.522   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.783   0.253   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.527   5.901   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.763   7.238   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.777   7.245   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.553   5.914   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.789   4.577   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.751   4.571   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.432   3.123   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.512   1.577   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.824   3.437   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -3.228   4.070   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.061   5.601   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.168   8.724   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.505   9.488   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.279  11.076   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.991   9.083   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.990  10.338   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.755   7.746   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7    3   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13    6   14   18                                                  
CONECT   14   13   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   21                                                  
CONECT   18   17   13   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   17   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   16                                                       
CONECT   24   14   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27    5                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Value	Source
Rubschisandrin	Kegg
(-)-gamma-Schizandrin	Kegg
(-)-g-Schizandrin	Generator
(-)-Γ-schizandrin	Generator

Chemical Formula

C₂₃H₂₈O₆

Average Mass

400.4710 Da

Monoisotopic Mass

400.18859 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C(OC)=C1OC)C1=C(C[C@@H](C)[C@@H](C)C2)C=C2OCOC2=C1OC

InChI Identifier

InChI=1S/C23H28O6/c1-12-7-14-9-16(24-3)20(25-4)22(26-5)18(14)19-15(8-13(12)2)10-17-21(23(19)27-6)29-11-28-17/h9-10,12-13H,7-8,11H2,1-6H3/t12-,13+/m0/s1

InChI Key

RTZKSTLPRTWFEV-QWHCGFSZSA-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
Kadsura coccinea	LOTUS Database	35616633
Kadsura interior	LOTUS Database	35616633
Schisandra chinensis	LOTUS Database	35616633
Schisandra lancifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Dibenzocyclooctane lignan
Benzodioxole
Anisole
Alkyl aryl ether
Benzenoid
Oxacycle
Organoheterocyclic compound
Ether
Acetal
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

tannin (CHEBI:5517 )
Lignans (C10621 )

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

C00002606

Chemspider ID

152036

KEGG Compound ID

C10621

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

174277

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene (NP0153460)

MOL for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)

3D MOL for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)

3D SDF for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)

3D-SDF for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)

PDB for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)

3D PDB for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)

SMILES for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)

INCHI for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)

Structure for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)

3D Structure for NP0153460 ((9s,10r)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2(7),3,5,13,18-hexaene)