NP-MRD: Showing NP-Card for 3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde (NP0202461)

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Record Information

Version

2.0

Created at

2022-09-04 21:41:02 UTC

Updated at

2022-09-04 21:41:02 UTC

NP-MRD ID

NP0202461

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde

Description

6,6,10,11-Tetramethyl-14-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-2-carbaldehyde belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde is found in Gymnema sylvestre. 6,6,10,11-Tetramethyl-14-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-2-carbaldehyde is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241518282D          

 64 70  0  0  0  0            999 V2000
    7.8992   -0.4075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2479    0.0988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4837   -0.2121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8323    0.2943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9452    1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939    1.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6425    2.1242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8002    2.2692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6175    2.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1238    2.8077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9411    2.6948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4474    3.3462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2647    3.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7710    3.8847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4601    4.6488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9665    5.3002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7837    5.1873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2901    5.8386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0946    4.4231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9119    4.3103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5883    3.7718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8992    3.0076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2520    1.9307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0692    1.8178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7456    1.2793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0565    0.5152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9284    1.3922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4220    0.7409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4850   -0.5835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1814   -0.6920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2793   -0.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7182   -1.1380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069    1.3336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.1221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4416    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2537    0.6076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5976    1.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8779    0.3171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5052    2.0142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0370    2.6449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6931    2.1594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4128    2.9353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1613    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3492    1.6739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3607    0.9161    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
  6  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
 11 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
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  9 27  1  0  0  0  0
 27 28  1  0  0  0  0
  6 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
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 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
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 36 37  1  0  0  0  0
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 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 37 49  1  0  0  0  0
 42 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
 46 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 55 58  1  0  0  0  0
 58 59  1  0  0  0  0
 58 60  1  0  0  0  0
 60 61  1  0  0  0  0
 60 62  1  0  0  0  0
 53 62  1  0  0  0  0
 62 63  1  0  0  0  0
  2 64  1  0  0  0  0
M  END

     RDKit          3D

142148  0  0  0  0  0  0  0  0999 V2000
    6.2182    5.6855   -1.7860 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0382    4.7875   -2.0908 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2509    5.1043   -3.3067 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7707    3.7888   -1.2859 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6167    2.8929   -1.5643 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0325    1.4807   -1.7430 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8938    0.4892   -2.0596 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2237    0.9691   -3.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2490   -0.7130   -2.1773 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4790   -1.9255   -2.3069 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0847   -2.6410   -1.2384 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3175   -3.1285   -1.4982 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0649   -3.1586   -0.1439 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0974   -1.8374    0.3062 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9203   -1.1749    2.4610 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.8211   -0.4337    3.7693 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2243    0.7285    4.4545 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4782    0.5271   -1.6910 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004241518282D          

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M  END
> <DATABASE_ID>
NP0202461

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC(C)(OC1OC(COC2OCC(O)C(O)C2O)C(O)C(O)C1O)C1CCC2(C)C1CCC1C2(C)CCC2C(C)(C)C(CCC12C=O)OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C47H78O17/c1-23(2)9-8-15-46(7,64-42-39(58)36(55)34(53)28(62-42)21-60-40-37(56)32(51)26(50)20-59-40)25-12-16-44(5)24(25)10-11-30-45(44,6)17-13-29-43(3,4)31(14-18-47(29,30)22-49)63-41-38(57)35(54)33(52)27(19-48)61-41/h9,22,24-42,48,50-58H,8,10-21H2,1-7H3

> <INCHI_KEY>
HQHTWUILTRHXDO-UHFFFAOYSA-N

> <FORMULA>
C47H78O17

> <MOLECULAR_WEIGHT>
915.124

> <EXACT_MASS>
914.523901052

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
142

> <JCHEM_AVERAGE_POLARIZABILITY>
99.55618779261624

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6,6,10,11-tetramethyl-14-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-2-carbaldehyde

> <ALOGPS_LOGP>
1.50

> <JCHEM_LOGP>
1.1916069536666674

> <ALOGPS_LOGS>
-3.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.20254607607116

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.75752280480825

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6483775368396385

> <JCHEM_POLAR_SURFACE_AREA>
274.74999999999994

> <JCHEM_REFRACTIVITY>
227.71260000000012

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.57e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,6,10,11-tetramethyl-14-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-2-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      14.745  -0.761   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.529   0.184   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.103  -0.396   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.887   0.549   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.098   2.075   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.882   3.020   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.666   3.965   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.827   4.236   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      12.353   4.025   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      13.298   5.241   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      14.823   5.030   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.769   6.246   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      17.294   6.036   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      18.239   7.251   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      17.659   8.678   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      18.604   9.894   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      20.130   9.683   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      21.075  10.899   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      20.710   8.257   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      22.235   8.046   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      19.765   7.041   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      20.345   5.614   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      15.404   3.604   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      16.929   3.393   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      14.458   2.388   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      15.039   0.962   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      12.933   2.599   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.988   1.383   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.937   1.804   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.365   0.325   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.090  -0.539   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.874   0.406   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.505  -1.089   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.398   1.854   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.405   3.032   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.889   2.761   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.366   1.312   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.358   0.135   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.939  -1.292   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       4.835  -1.314   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.319  -1.585   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -0.521  -1.452   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.341  -2.124   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -0.182   0.499   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       0.341   1.947   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       1.857   2.218   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       2.850   1.041   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       3.373   2.489   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       2.380   3.667   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0      -1.698   0.228   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      -2.691   1.405   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      -4.207   1.134   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      -5.200   2.311   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      -6.716   2.040   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      -7.239   0.592   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      -4.676   3.760   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      -5.669   4.937   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0      -3.160   4.031   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0      -2.637   5.479   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0      -2.168   2.854   0.000  0.00  0.00           C+0
HETATM   63  O   UNK     0      -0.652   3.125   0.000  0.00  0.00           O+0
HETATM   64  C   UNK     0      13.740   1.710   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   64                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   29                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   27                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   23                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   14   22                                                  
CONECT   22   21                                                            
CONECT   23   11   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    9   28                                                  
CONECT   28   27                                                            
CONECT   29    6   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   38                                             
CONECT   33   32                                                            
CONECT   34   32   29   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   49                                                  
CONECT   38   37   32   39   40                                             
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   49                                                  
CONECT   43   42   44   45   46                                             
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   43   47   52                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   37   42   50                                             
CONECT   50   49   51                                                       
CONECT   51   50                                                            
CONECT   52   46   53                                                       
CONECT   53   52   54   62                                                  
CONECT   54   53   55                                                       
CONECT   55   54   56   58                                                  
CONECT   56   55   57                                                       
CONECT   57   56                                                            
CONECT   58   55   59   60                                                  
CONECT   59   58                                                            
CONECT   60   58   61   62                                                  
CONECT   61   60                                                            
CONECT   62   60   53   63                                                  
CONECT   63   62                                                            
CONECT   64    2                                                            
MASTER        0    0    0    0    0    0    0    0   64    0  140    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₇H₇₈O₁₇

Average Mass

915.1240 Da

Monoisotopic Mass

914.52390 Da

IUPAC Name

6,6,10,11-tetramethyl-14-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-2-carbaldehyde

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)(OC1OC(COC2OCC(O)C(O)C2O)C(O)C(O)C1O)C1CCC2(C)C1CCC1C2(C)CCC2C(C)(C)C(CCC12C=O)OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C47H78O17/c1-23(2)9-8-15-46(7,64-42-39(58)36(55)34(53)28(62-42)21-60-40-37(56)32(51)26(50)20-59-40)25-12-16-44(5)24(25)10-11-30-45(44,6)17-13-29-43(3,4)31(14-18-47(29,30)22-49)63-41-38(57)35(54)33(52)27(19-48)61-41/h9,22,24-42,48,50-58H,8,10-21H2,1-7H3

InChI Key

HQHTWUILTRHXDO-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
Gymnema sylvestre	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
19-oxosteroid
Oxosteroid
Steroid
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Disaccharide
O-glycosyl compound
Glycosyl compound
Fatty acyl
Oxane
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Polyol
Acetal
Hydrocarbon derivative
Organooxygen compound
Primary alcohol
Organic oxygen compound
Carbonyl group
Organic oxide
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	1.5	ALOGPS
logP	1.19	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	11.76	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	274.75 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	227.71 m³·mol⁻¹	ChemAxon
Polarizability	99.56 Å³	ChemAxon
Number of Rings	7	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde (NP0202461)

MOL for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D MOL for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D SDF for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D-SDF for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

PDB for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D PDB for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

SMILES for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

INCHI for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

Structure for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D Structure for NP0202461 (3a,3b,6,6-tetramethyl-1-{6-methyl-2-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl)oxy]hept-5-en-2-yl}-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)