NP-MRD: Showing NP-Card for 1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one (NP0247464)

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Record Information

Version

2.0

Created at

2022-09-07 09:19:31 UTC

Updated at

2022-09-07 09:19:31 UTC

NP-MRD ID

NP0247464

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one

Description

1-[6',6'-Bis(hydroxymethyl)-2',3,11',15'-tetramethyl-5'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}spiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan]-1'(10')-en-5-yl]propan-1-one belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one is found in Muscari armeniacum. 1-[6',6'-Bis(hydroxymethyl)-2',3,11',15'-tetramethyl-5'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}spiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan]-1'(10')-en-5-yl]propan-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201500372D          

 45 50  0  0  0  0            999 V2000
    8.0826   -0.4408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2584   -0.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8778    0.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3215    1.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0536    0.3640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5397   -0.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8445    0.0953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0789   -0.4470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8035    0.8322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8400    1.6564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0674    1.9457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5535    1.3004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1729    2.0324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7300    1.2505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3614    0.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8164   -0.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6399   -0.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0084    0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5328   -0.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5380    0.4624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1694   -0.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4515    1.8887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2750    1.9387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5987    1.0522    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
  3  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 17 18  1  0  0  0  0
  9 18  1  0  0  0  0
 12 18  1  0  0  0  0
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 31 33  1  0  0  0  0
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 33 35  1  0  0  0  0
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 24 37  1  0  0  0  0
 37 38  1  0  0  0  0
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 43 44  1  0  0  0  0
 14 44  1  0  0  0  0
  9 45  1  0  0  0  0
  5 45  1  0  0  0  0
M  END

     RDKit          3D

101106  0  0  0  0  0  0  0  0999 V2000
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 45  5  1  0
 18  9  1  0
 42 20  1  0
 18 12  1  0
 35 26  1  0
 44 14  1  0
  1 46  1  0
  1 47  1  0
  1 48  1  0
  2 49  1  0
  2 50  1  0
  5 51  1  1
  6 52  1  0
  6 53  1  0
  7 54  1  1
  8 55  1  0
  8 56  1  0
  8 57  1  0
 10 58  1  0
 10 59  1  0
 11 60  1  0
 11 61  1  0
 13 62  1  0
 13 63  1  0
 13 64  1  0
 16 65  1  0
 16 66  1  0
 17 67  1  0
 17 68  1  0
 19 69  1  0
 19 70  1  0
 19 71  1  0
 21 72  1  0
 21 73  1  0
 21 74  1  0
 22 75  1  0
 22 76  1  0
 23 77  1  0
 23 78  1  0
 24 79  1  1
 26 80  1  1
 28 81  1  6
 29 82  1  0
 29 83  1  0
 30 84  1  0
 31 85  1  1
 32 86  1  0
 33 87  1  1
 34 88  1  0
 35 89  1  6
 36 90  1  0
 38 91  1  0
 38 92  1  0
 39 93  1  0
 40 94  1  0
 40 95  1  0
 41 96  1  0
 42 97  1  1
 43 98  1  0
 43 99  1  0
 44100  1  0
 44101  1  0
M  END


  Mrv1533004201500372D          

 45 50  0  0  0  0            999 V2000
    8.0826   -0.4408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2584   -0.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8778    0.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3215    1.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0536    0.3640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5397   -0.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8445    0.0953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0789   -0.4470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8035    0.8322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8400    1.6564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0674    1.9457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5535    1.3004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1729    2.0324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7300    1.2505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3614    0.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8164   -0.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6399   -0.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0084    0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5328   -0.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5380    0.4624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9929   -0.2258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1694   -0.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3460   -0.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1090    0.3626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9325    0.3127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3010   -0.4255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8460   -1.1137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2146   -1.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7596   -2.5400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0639   -2.4901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0381   -1.9017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4066   -2.6398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4930   -1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3165   -1.2634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1245   -0.4754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5795    0.2128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2595    1.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5314    1.3354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7236    2.1378    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3533    1.9203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3096    2.4114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0830    1.1506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4515    1.8887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2750    1.9387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5987    1.0522    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
  3  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  9 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 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
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 26 35  1  0  0  0  0
 35 36  1  0  0  0  0
 24 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 40  1  0  0  0  0
 40 41  1  0  0  0  0
 37 42  1  0  0  0  0
 20 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 14 44  1  0  0  0  0
  9 45  1  0  0  0  0
  5 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0247464

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC23C)C2(C)CCC(OC3OC(CO)C(O)C(O)C3O)C(CO)(CO)C2CC4)O1

> <INCHI_IDENTIFIER>
InChI=1S/C35H56O10/c1-6-22(39)23-15-19(2)35(45-23)14-13-32(4)21-7-8-25-31(3,20(21)9-12-33(32,35)5)11-10-26(34(25,17-37)18-38)44-30-29(42)28(41)27(40)24(16-36)43-30/h19,23-30,36-38,40-42H,6-18H2,1-5H3

> <INCHI_KEY>
XSKQDKQMKQAAST-UHFFFAOYSA-N

> <FORMULA>
C35H56O10

> <MOLECULAR_WEIGHT>
636.823

> <EXACT_MASS>
636.387348003

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
71.56856544007182

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[6',6'-bis(hydroxymethyl)-2',3,11',15'-tetramethyl-5'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}spiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-en-5-yl]propan-1-one

> <ALOGPS_LOGP>
2.05

> <JCHEM_LOGP>
1.5229288383333306

> <ALOGPS_LOGS>
-3.69

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.18648899001866

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.208967470307714

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8204146681997777

> <JCHEM_POLAR_SURFACE_AREA>
166.14

> <JCHEM_REFRACTIVITY>
165.18340000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.31e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[6',6'-bis(hydroxymethyl)-2',3,11',15'-tetramethyl-5'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}spiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-en-5-yl]propan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      15.087  -0.823   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.549  -0.755   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.839   0.612   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      13.667   1.910   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.300   0.680   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.341  -0.525   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.043   0.178   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.614  -0.834   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.967   1.553   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.035   3.092   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.592   3.632   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.633   2.427   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.923   3.794   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.096   2.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.408   0.956   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.257  -0.328   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.794  -0.235   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.482   1.143   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.461  -0.046   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.871   0.863   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.720  -0.421   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.183  -0.515   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.646  -0.608   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.203   0.677   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.741   0.584   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -2.429  -0.794   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.579  -2.079   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -2.267  -3.457   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.418  -4.741   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.119  -4.648   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -3.804  -3.550   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -4.492  -4.928   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -4.654  -2.265   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -6.191  -2.358   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -3.966  -0.887   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -4.815   0.397   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       0.484   2.055   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -0.992   2.493   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -1.351   3.990   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       0.660   3.585   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -0.578   4.501   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       2.022   2.148   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.709   3.526   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.247   3.619   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      10.451   1.964   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   45                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   18   45                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   18                                             
CONECT   13   12                                                            
CONECT   14   12   15   44                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    9   12   19                                             
CONECT   19   18                                                            
CONECT   20   15   21   22   42                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   37                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   35                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   26   36                                                  
CONECT   36   35                                                            
CONECT   37   24   38   40   42                                             
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   37   41                                                       
CONECT   41   40                                                            
CONECT   42   37   20   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43   14                                                       
CONECT   45    9    5                                                       
MASTER        0    0    0    0    0    0    0    0   45    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₆O₁₀

Average Mass

636.8230 Da

Monoisotopic Mass

636.38735 Da

IUPAC Name

1-[6',6'-bis(hydroxymethyl)-2',3,11',15'-tetramethyl-5'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}spiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-en-5-yl]propan-1-one

Traditional Name

CAS Registry Number

Not Available

SMILES

CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC23C)C2(C)CCC(OC3OC(CO)C(O)C(O)C3O)C(CO)(CO)C2CC4)O1

InChI Identifier

InChI=1S/C35H56O10/c1-6-22(39)23-15-19(2)35(45-23)14-13-32(4)21-7-8-25-31(3,20(21)9-12-33(32,35)5)11-10-26(34(25,17-37)18-38)44-30-29(42)28(41)27(40)24(16-36)43-30/h19,23-30,36-38,40-42H,6-18H2,1-5H3

InChI Key

XSKQDKQMKQAAST-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

Species Name	Source	Reference
Muscari armeniacum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Steroidal glycoside
Steroid
Glycosyl compound
O-glycosyl compound
Oxane
Monosaccharide
Tetrahydrofuran
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Dialkyl ether
Ether
Polyol
Acetal
Hydrocarbon derivative
Alcohol
Organooxygen compound
Primary alcohol
Organic oxygen compound
Carbonyl group
Organic oxide
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	2.05	ALOGPS
logP	1.52	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	166.14 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	165.18 m³·mol⁻¹	ChemAxon
Polarizability	71.57 Å³	ChemAxon
Number of Rings	6	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

14263467

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one (NP0247464)

MOL for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)

3D MOL for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)

3D SDF for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)

3D-SDF for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)

PDB for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)

3D PDB for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)

SMILES for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)

INCHI for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)

Structure for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)

3D Structure for NP0247464 (1-[6,6-bis(hydroxymethyl)-3',3a,9a,11a-tetramethyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3,4,5,5a,7,8,9,10,11-decahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxolan]-5'-yl]propan-1-one)