NP-MRD: Showing NP-Card for 2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0263480)

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Record Information

Version

2.0

Created at

2022-09-08 06:40:24 UTC

Updated at

2022-09-08 06:40:25 UTC

NP-MRD ID

NP0263480

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

2-{[3,5-Dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]Tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated. 2-{[3,5-Dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]Tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191518252D          

 55 62  0  0  0  0            999 V2000
   -0.9503   -1.9228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3707   -1.3358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4276   -1.5442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0072   -0.9572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7983   -0.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4185    0.4168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3042    0.3050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2111    0.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5884    0.2512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2035    1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3246    1.1382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2426   -0.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6803   -1.2726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4993   -1.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8575   -0.4418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6811   -0.3946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3102   -1.1315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1338   -1.0843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9575   -1.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3284   -0.3003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1521   -0.2531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5230    0.4838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0703    1.1735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4413    1.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9886    2.6001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3595    3.3370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2649    1.9576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6359    2.6945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7176    1.2679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5413    1.3151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9940    0.6254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6230   -0.1115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0757   -0.8012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7048   -1.5381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8811   -1.5853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8994   -0.7540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3521   -1.4437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2703   -0.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0940    0.0301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8176    0.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1886    1.4095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3467    0.5310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7994   -0.1587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8757    0.3895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6336    0.7155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6862    1.1924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0521    0.3423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5994    1.0320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7757    0.9848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4048    0.2479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9734    0.9511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4170   -0.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8116   -1.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0382   -1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5893   -0.5403    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
  4  5  1  0  0  0  0
  5  6  1  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
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 31 40  1  0  0  0  0
 40 41  1  0  0  0  0
 29 42  1  0  0  0  0
 22 42  1  0  0  0  0
 42 43  1  0  0  0  0
 20 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 44 47  1  0  0  0  0
 16 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
  9 50  1  0  0  0  0
 15 50  1  0  0  0  0
 50 51  1  0  0  0  0
 12 52  1  0  0  0  0
  7 52  1  0  0  0  0
 52 53  2  0  0  0  0
  4 53  1  0  0  0  0
 53 54  1  0  0  0  0
  2 55  1  0  0  0  0
M  END

     RDKit          3D

121128  0  0  0  0  0  0  0  0999 V2000
  -11.3963    2.4866    0.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4426    2.4540   -0.9016 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7035    3.4013   -2.0466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3927    1.6411   -0.9403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1041    0.7093    0.1515 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.1247   -0.7537   -0.2821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0590   -1.1462   -1.0121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8336   -0.7303   -0.7196 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8868   -1.7950   -0.1093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7162   -0.8620   -0.1221 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7559   -0.4737   -1.5697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1176   -0.3374   -1.8322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2788    0.2852    0.7411 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4509    1.4638    0.3893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0206    1.1858    0.7058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4907   -0.1207    0.2476 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1022   -0.4215    0.6901 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8621   -0.5357    2.1418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2387    0.7574    0.2056 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2065    0.5647    0.4691 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7758   -0.7923    0.2557 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8032   -0.7066   -0.6622 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0599   -0.9324   -0.2119 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5320   -2.1048   -0.7877 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4549   -1.9334   -1.7865 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6791   -3.1417   -2.6300 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1371   -4.2382   -1.8964 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7619   -1.4941   -1.1624 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4780   -0.8227   -2.1635 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4367    0.5527   -0.1317 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1971    0.5940    1.0080 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0685    1.8273    1.6346 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.2256    3.6169    0.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6290    4.7253   -0.4294 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4518    2.6407   -0.1884 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8402    2.4124   -1.4351 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3590    1.4830    0.0838 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.5136    1.9002    0.7863 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6676    0.3446    0.7823 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.2517    0.2296    2.0633 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0579    0.1433   -0.3424 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8956    1.1532    0.6372 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8246   -1.9046   -0.0187 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2461   -2.4685   -1.3950 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0671   -3.1061    0.9166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6077   -1.5811   -0.1291 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4456   -2.7852    0.2119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8559   -2.4910   -0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.7903    3.5196   -2.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.8982    0.8024    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0545   -0.8617   -0.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.7891   -2.6444   -0.8019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4382   -1.3786   -2.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1434    0.3576   -1.8781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0839    0.0569    1.8095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7597    2.3138    1.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6232    1.8772   -0.6251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4477    1.9841    0.1416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8355    1.3928    1.7784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4150   -0.0438   -0.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3349    0.3192    2.6527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1064   -1.4652    2.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2423   -0.3873    2.3155 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2770   -1.0583    1.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5284   -0.9405    0.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.9279    3.6425    1.5944 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5564    3.9483    1.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004191518252D          

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M  END
> <DATABASE_ID>
NP0263480

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC1COC23CC4(CO2)C(CCC2C5(C)CCC(OC6OC(CO)C(O)C(OC7OC(CO)C(O)C(O)C7O)C6O)C(C)(C)C5CCC42C)C3=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C42H66O13/c1-20(2)14-22-17-50-42-18-41(19-51-42)23(29(42)21(22)3)8-9-27-39(6)12-11-28(38(4,5)26(39)10-13-40(27,41)7)54-37-34(49)35(31(46)25(16-44)53-37)55-36-33(48)32(47)30(45)24(15-43)52-36/h14,22-28,30-37,43-49H,8-13,15-19H2,1-7H3

> <INCHI_KEY>
FFMPHFWEPCKMLS-UHFFFAOYSA-N

> <FORMULA>
C42H66O13

> <MOLECULAR_WEIGHT>
778.977

> <EXACT_MASS>
778.450342185

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
121

> <JCHEM_AVERAGE_POLARIZABILITY>
87.47525307965505

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
2.06

> <JCHEM_LOGP>
2.0421661876666644

> <ALOGPS_LOGS>
-3.87

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.458507761181835

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.940027511627463

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835653396

> <JCHEM_POLAR_SURFACE_AREA>
196.98999999999998

> <JCHEM_REFRACTIVITY>
199.0183000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.06e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -1.774  -3.589   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.692  -2.493   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.798  -2.883   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.880  -1.787   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.490  -0.296   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.648   0.778   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.301   0.569   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.994   1.268   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.698   0.469   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.980   2.314   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.339   2.125   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.053  -1.061   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.870  -2.376   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.399  -2.230   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.067  -0.825   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.605  -0.737   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.912  -2.112   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.450  -2.024   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.987  -1.936   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.680  -0.560   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      15.217  -0.472   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      15.910   0.903   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      15.065   2.191   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      15.757   3.566   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      14.912   4.854   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      15.604   6.229   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      17.295   3.654   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      17.987   5.030   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      18.140   2.367   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      19.677   2.455   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      20.522   1.167   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      19.830  -0.208   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      20.675  -1.496   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      19.982  -2.871   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      18.445  -2.959   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      22.212  -1.407   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      23.057  -2.695   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      22.905  -0.032   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      24.442   0.056   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      22.060   1.256   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      22.752   2.631   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      17.447   0.991   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      18.292  -0.296   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      12.835   0.727   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      14.249   1.336   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      12.481   2.226   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      11.297   0.639   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      10.452   1.926   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       8.915   1.838   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       8.222   0.463   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       7.417   1.775   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       4.512  -0.997   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       3.382  -2.159   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       3.805  -3.640   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      -1.100  -1.008   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   55                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   53                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   11   52                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   12   50                                             
CONECT   10    9   11                                                       
CONECT   11   10    7                                                       
CONECT   12    9   13   52                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   50                                                  
CONECT   16   15   17   18   47                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   44                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   42                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   42                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   40                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   36                                                  
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   33   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   31   41                                                  
CONECT   41   40                                                            
CONECT   42   29   22   43                                                  
CONECT   43   42                                                            
CONECT   44   20   45   46   47                                             
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47   44   16   48                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49    9   15   51                                             
CONECT   51   50                                                            
CONECT   52   12    7   53                                                  
CONECT   53   52    4   54                                                  
CONECT   54   53                                                            
CONECT   55    2                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  124    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₆₆O₁₃

Average Mass

778.9770 Da

Monoisotopic Mass

778.45034 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)=CC1COC23CC4(CO2)C(CCC2C5(C)CCC(OC6OC(CO)C(O)C(OC7OC(CO)C(O)C(O)C7O)C6O)C(C)(C)C5CCC42C)C3=C1C

InChI Identifier

InChI=1S/C42H66O13/c1-20(2)14-22-17-50-42-18-41(19-51-42)23(29(42)21(22)3)8-9-27-39(6)12-11-28(38(4,5)26(39)10-13-40(27,41)7)54-37-34(49)35(31(46)25(16-44)53-37)55-36-33(48)32(47)30(45)24(15-43)52-36/h14,22-28,30-37,43-49H,8-13,15-19H2,1-7H3

InChI Key

FFMPHFWEPCKMLS-UHFFFAOYSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Diterpene glycosides

Alternative Parents

Substituents

Diterpene glycoside
Diterpenoid
Steroid
Naphthopyran
Disaccharide
Glycosyl compound
O-glycosyl compound
Naphthalene
Ketal
Pyran
Oxane
Tetrahydrofuran
Secondary alcohol
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organooxygen compound
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	2.06	ALOGPS
logP	2.04	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	11.94	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	196.99 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	199.02 m³·mol⁻¹	ChemAxon
Polarizability	87.48 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73310398

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0263480)

MOL for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0263480 (2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-{[2,6,6,10,16-pentamethyl-17-(2-methylprop-1-en-1-yl)-19,21-dioxahexacyclo[18.2.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-15-en-7-yl]oxy}oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)