NP-MRD: Showing NP-Card for (2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one (NP0209488)

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Record Information

Version

2.0

Created at

2022-09-05 06:54:51 UTC

Updated at

2022-09-05 06:54:52 UTC

NP-MRD ID

NP0209488

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one

Description

Isoptaquiloside belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. (2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one is found in Pteridium aquilinum and Pteridium caudatum. (2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one was first documented in 2003 (PMID: 12696937). Based on a literature review very few articles have been published on Isoptaquiloside.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052208542D          

 28 31  0  0  1  0            999 V2000
    1.9347    1.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5169    0.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3142    0.8926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5293    1.6891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9471    2.2736    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1498    2.0617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5676    2.6462    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7702    2.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1880    3.0187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7827    3.4426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2005    4.0272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5800    3.6546    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7951    4.4511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1622    3.0701    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9595    3.2820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8964    0.3081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7203    0.3497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0145   -0.4211    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8109   -0.6362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3723   -0.9391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4138   -1.7630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6813   -0.4884    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8840   -0.7003    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2312   -1.4487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2072   -1.1722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3018   -0.1158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7173   -0.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5053    0.0993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  1  0  0  0
  3 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 22 20  1  6  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  1  0  0  0
 23 26  1  0  0  0  0
  2 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
    0.6953    2.1688    0.3774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5683    1.4550    0.0598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5802    0.3925   -0.7704 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6294    0.0242   -1.2861 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5327   -0.9083   -0.7609 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9995   -0.6125    0.5081 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3729   -0.7658    0.6293 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7859   -0.5253    2.0700 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1645   -0.6782    2.1965 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0882    0.1910   -0.2727 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4760    0.1089   -0.0467 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7631   -0.1522   -1.6875 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4905    1.0359   -2.3632 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6450   -1.1289   -1.7576 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0848   -2.4711   -1.7583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8833   -0.2074   -0.9963 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9030   -1.6122   -1.5114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3751   -1.9694   -1.2297 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5319   -3.3904   -0.8092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7714   -1.0931   -0.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9174   -1.0049    0.3020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5330   -0.4532    0.3553 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6846    0.7755    1.1757 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1095    1.2181    1.3404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2027    0.4887    2.4580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8202    1.9253    0.6634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3987    3.2405    0.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7016    3.0548    1.6823 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5694    3.2710    0.3126 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4956    1.9367   -0.3807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0719    1.8321    1.3456 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0025   -1.8810   -0.6791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7205   -1.7950    0.3838 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3282   -1.3219    2.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4808    0.4740    2.4376 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5465    0.1301    2.6236 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7501    1.2139   -0.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8627    0.8854   -0.5385 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6773   -0.6395   -2.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9008    0.9652   -3.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1657   -1.0042   -2.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0285   -2.5591   -1.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5482    0.3859   -1.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6465   -1.7287   -2.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3311   -2.3305   -0.8709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9154   -1.7305   -2.1638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7927   -3.5021    0.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4304   -3.8049   -1.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6367   -4.0156   -0.9681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9026   -1.2387    0.8532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0883    2.1880    1.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5837    0.4937    2.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6630    1.3164    0.4072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3794   -0.4466    2.7078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8733    3.8644   -0.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4810    3.3859    0.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7148    3.4998    1.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3601    3.0493    2.5696 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 22  1  0
 22 20  1  0
 20 21  2  0
 22 23  1  0
 23 24  1  0
 23 25  1  1
 23 26  1  0
 26 27  1  0
 27 28  1  0
 26  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 20 18  1  0
 28 26  1  0
 14  5  1  0
  3 16  1  0
 19 47  1  0
 19 48  1  0
 19 49  1  0
 18 46  1  6
 17 44  1  0
 17 45  1  0
 16 43  1  6
 22 50  1  1
 24 51  1  0
 24 52  1  0
 24 53  1  0
 25 54  1  0
 27 55  1  0
 27 56  1  0
 28 57  1  0
 28 58  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  5 32  1  1
  7 33  1  6
  8 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  1
 11 38  1  0
 12 39  1  6
 13 40  1  0
 14 41  1  6
 15 42  1  0
M  END


  Mrv1652309052208542D          

 28 31  0  0  1  0            999 V2000
    1.9347    1.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5169    0.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3142    0.8926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5293    1.6891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9471    2.2736    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1498    2.0617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5676    2.6462    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7702    2.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1880    3.0187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7827    3.4426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2005    4.0272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5800    3.6546    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7951    4.4511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1622    3.0701    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9595    3.2820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8964    0.3081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7203    0.3497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0145   -0.4211    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8109   -0.6362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3723   -0.9391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4138   -1.7630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6813   -0.4884    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8840   -0.7003    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2312   -1.4487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2072   -1.1722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3018   -0.1158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7173   -0.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5053    0.0993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  1  0  0  0
  3 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 22 20  1  6  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  1  0  0  0
 23 26  1  0  0  0  0
  2 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0209488

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC2[C@H](C1=O)[C@@](C)(O)C1(CC1)C(C)=C2O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O8/c1-8-6-10-12(13(8)22)19(3,26)20(4-5-20)9(2)17(10)28-18-16(25)15(24)14(23)11(7-21)27-18/h8,10-12,14-16,18,21,23-26H,4-7H2,1-3H3/t8-,10?,11-,12-,14-,15+,16-,18+,19-/m1/s1

> <INCHI_KEY>
NUQBCPSNXCIWAM-RPZIKLKPSA-N

> <FORMULA>
C20H30O8

> <MOLECULAR_WEIGHT>
398.452

> <EXACT_MASS>
398.194067926

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.847485772236304

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2'R,3'aS,4'R)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3',3'a,4',7'a-hexahydrospiro[cyclopropane-1,5'-indene]-3'-one

> <JCHEM_LOGP>
-0.997453718999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.14920647791567

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.1950709049785

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092151233301

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
97.74619999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2'R,3'aS,4'R)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-indene]-3'-one

> <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       3.611   2.362   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.698   1.271   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.186   1.666   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.588   3.153   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.501   4.244   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.013   3.848   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.926   4.940   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.438   4.544   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.351   5.635   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.328   6.426   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.241   7.517   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.816   6.822   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.217   8.309   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.903   5.731   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.391   6.126   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.273   0.575   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.811   0.653   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.360  -0.786   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.847  -1.188   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.162  -1.753   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.239  -3.291   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.872  -0.912   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.383  -1.307   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.031  -2.704   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.120  -2.188   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.297  -0.216   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.206  -1.303   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.810   0.185   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   26                                                  
CONECT    3    2    4   16                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   14                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    5   15                                                  
CONECT   15   14                                                            
CONECT   16    3   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   16   23                                                  
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23    2   27   28                                             
CONECT   27   26   28                                                       
CONECT   28   27   26                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₈

Average Mass

398.4520 Da

Monoisotopic Mass

398.19407 Da

IUPAC Name

(2'R,3'aS,4'R)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3',3'a,4',7'a-hexahydrospiro[cyclopropane-1,5'-indene]-3'-one

Traditional Name

(2'R,3'aS,4'R)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-indene]-3'-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC2[C@H](C1=O)[C@@](C)(O)C1(CC1)C(C)=C2O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C20H30O8/c1-8-6-10-12(13(8)22)19(3,26)20(4-5-20)9(2)17(10)28-18-16(25)15(24)14(23)11(7-21)27-18/h8,10-12,14-16,18,21,23-26H,4-7H2,1-3H3/t8-,10?,11-,12-,14-,15+,16-,18+,19-/m1/s1

InChI Key

NUQBCPSNXCIWAM-RPZIKLKPSA-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
Pteridium aquilinum	LOTUS Database	35616633
Pteridium caudatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Hexose monosaccharide
O-glycosyl compound
Monosaccharide
Oxane
Tertiary alcohol
Secondary alcohol
Ketone
Polyol
Organoheterocyclic compound
Oxacycle
Acetal
Primary alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Aldehyde
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	ChemAxon
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	97.75 m³·mol⁻¹	ChemAxon
Polarizability	40.85 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

102065499

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Castillo UF, Wilkins AL, Lauren DR, Smith BL, Alonso-Amelot M: Pteroside A2--a new illudane-type sesquiterpene glucoside from pteridium caudatum L. Maxon, and the spectrometric characterization of caudatodienone. J Agric Food Chem. 2003 Apr 23;51(9):2559-64. doi: 10.1021/jf026238j. [PubMed:12696937 ]
LOTUS database [Link]

Showing NP-Card for (2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one (NP0209488)

MOL for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)

3D MOL for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)

3D SDF for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)

3D-SDF for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)

PDB for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)

3D PDB for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)

SMILES for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)

INCHI for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)

Structure for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)

3D Structure for NP0209488 ((2'r,3'as,4'r)-4'-hydroxy-2',4',6'-trimethyl-7'-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1',2',3'a,7'a-tetrahydrospiro[cyclopropane-1,5'-inden]-3'-one)