NP-MRD: Showing NP-Card for 6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione (NP0240227)

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Record Information

Version

2.0

Created at

2022-09-06 23:59:47 UTC

Updated at

2022-09-06 23:59:47 UTC

NP-MRD ID

NP0240227

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione

Description

6,7,34,35-Tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]Pentatriacontane-10,13-dione belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. 6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione is found in Pleopsidium gobiense. 6,7,34,35-Tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]Pentatriacontane-10,13-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004151517272D          

 47 50  0  0  0  0            999 V2000
    0.3117   -0.5637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1366   -0.5760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2565    0.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5836    0.9976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0955    1.6446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7574    2.1370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5242    2.4413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3437    2.5368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1599    2.4169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9174    2.0899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5643    1.5779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0567    0.9160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3610    0.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4565   -0.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3366   -1.4865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0096   -2.2439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7831   -2.5309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7492   -3.3552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3961   -3.8671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9548   -3.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6678   -4.3512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4977   -2.8909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8357   -3.3833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2375   -4.1038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0689   -3.6876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2495   -3.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5538   -4.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3700   -4.6698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8823   -3.6771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5553   -4.4345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3899   -3.0152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4295   -3.1107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9219   -2.4487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7170   -2.2578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5364   -2.1623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2321   -1.3955    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  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
 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
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 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 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
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 26 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 42 45  1  0  0  0  0
 45 46  1  0  0  0  0
 37 46  1  0  0  0  0
 46 47  1  0  0  0  0
  2 47  1  0  0  0  0
M  END

     RDKit          3D

103106  0  0  0  0  0  0  0  0999 V2000
   -1.7515    3.6880    1.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0701    2.8516    0.5436 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4119    3.1109    0.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7135    4.6016    0.4182 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836    4.8290   -0.5132 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9765    5.6228    0.1950 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3517    5.1653   -0.2420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7760    4.0187    0.6707 C   0  0  0  0  0  0  0  0  0  0  0  0
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 26 25  1  0
 25 23  1  0
 23 24  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 23 22  1  0
 37 38  1  0
 26 35  1  0
 21 80  1  0
 21 81  1  0
 21 82  1  0
 20 79  1  1
 22 83  1  6
 16 78  1  1
 15 76  1  0
 15 77  1  0
 14 74  1  0
 14 75  1  0
 13 72  1  0
 13 73  1  0
 12 70  1  0
 12 71  1  0
 11 68  1  0
 11 69  1  0
 10 66  1  0
 10 67  1  0
  9 64  1  0
  9 65  1  0
  8 62  1  0
  8 63  1  0
  7 60  1  0
  7 61  1  0
  6 58  1  0
  6 59  1  0
  5 56  1  0
  5 57  1  0
  4 54  1  0
  4 55  1  0
  3 52  1  0
  3 53  1  0
  2 51  1  6
  1 48  1  0
  1 49  1  0
  1 50  1  0
 38 95  1  1
 41 96  1  1
 42 97  1  0
 42 98  1  0
 43 99  1  0
 44100  1  6
 45101  1  0
 46102  1  6
 47103  1  0
 37 94  1  6
 35 93  1  1
 31 89  1  6
 32 90  1  0
 32 91  1  0
 33 92  1  0
 29 87  1  1
 30 88  1  0
 27 85  1  1
 28 86  1  0
 26 84  1  1
M  END


  Mrv1533004151517272D          

 47 50  0  0  0  0            999 V2000
    0.3117   -0.5637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1366   -0.5760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2565    0.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5836    0.9976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0955    1.6446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7574    2.1370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5242    2.4413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3437    2.5368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1599    2.4169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9174    2.0899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5643    1.5779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0567    0.9160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3610    0.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4565   -0.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3366   -1.4865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0096   -2.2439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7831   -2.5309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7492   -3.3552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3961   -3.8671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9548   -3.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6678   -4.3512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4977   -2.8909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8357   -3.3833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2375   -4.1038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0689   -3.6876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2495   -3.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5538   -4.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3700   -4.6698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0418   -5.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3461   -5.9637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2256   -5.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7137   -5.7240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0180   -6.4908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9213   -4.3102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4332   -3.6632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6758   -3.3362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0288   -2.8242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7018   -3.5817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1942   -4.2436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8823   -3.6771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5553   -4.4345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3899   -3.0152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4295   -3.1107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9219   -2.4487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7170   -2.2578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5364   -2.1623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2321   -1.3955    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  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
 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
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 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
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 26 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 42 45  1  0  0  0  0
 45 46  1  0  0  0  0
 37 46  1  0  0  0  0
 46 47  1  0  0  0  0
  2 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240227

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CCCCCCCCCCCCCC(C)OC3OC(CO)C(O)C(O)C3OC3OC(CO)C(O)C(O)C3OC2=O)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H56O14/c1-18-14-12-10-8-6-4-3-5-7-9-11-13-15-20-23(19(2)30(40)43-20)31(41)46-28-26(38)24(36)22(17-35)45-33(28)47-29-27(39)25(37)21(16-34)44-32(29)42-18/h18-29,32-39H,3-17H2,1-2H3

> <INCHI_KEY>
NFJPUMMCMMCPKZ-UHFFFAOYSA-N

> <FORMULA>
C33H56O14

> <MOLECULAR_WEIGHT>
676.797

> <EXACT_MASS>
676.367006483

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
71.9261318242773

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione

> <ALOGPS_LOGP>
2.05

> <JCHEM_LOGP>
2.447807198333333

> <ALOGPS_LOGS>
-2.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.962192113170858

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.399764856881301

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083765629662

> <JCHEM_POLAR_SURFACE_AREA>
210.89999999999998

> <JCHEM_REFRACTIVITY>
162.8052

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.54e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0       0.582  -1.052   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.122  -1.075   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.345   0.448   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.956   1.862   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.912   3.070   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.147   3.989   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.579   4.557   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.108   4.735   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.632   4.512   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.046   3.901   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.253   2.945   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.173   1.710   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.741   0.278   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.919  -1.251   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.695  -2.775   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.085  -4.189   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      14.528  -4.724   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      14.465  -6.263   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      15.673  -7.219   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      12.982  -6.678   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.447  -8.122   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.129  -5.396   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.893  -6.316   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.643  -7.661   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       9.462  -6.884   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.932  -7.062   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.500  -8.493   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.024  -8.717   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       7.545  -9.701   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.113 -11.132   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.021  -9.477   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.065 -10.685   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.634 -12.116   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       5.453  -8.046   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       6.409  -6.838   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       4.995  -6.228   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       3.787  -5.272   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.177  -6.686   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       4.096  -7.921   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       1.647  -6.864   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       1.037  -8.278   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       0.728  -5.628   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -0.802  -5.807   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -1.721  -4.571   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       1.338  -4.215   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       2.868  -4.036   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       2.300  -2.605   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   47                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   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                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   35                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   35                                                       
CONECT   35   34   26   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   46                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   45                                                  
CONECT   43   42   44                                                       
CONECT   44   43                                                            
CONECT   45   42   46                                                       
CONECT   46   45   37   47                                                  
CONECT   47   46    2                                                       
MASTER        0    0    0    0    0    0    0    0   47    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₅₆O₁₄

Average Mass

676.7970 Da

Monoisotopic Mass

676.36701 Da

IUPAC Name

6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione

Traditional Name

6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione

CAS Registry Number

Not Available

SMILES

CC1C2C(CCCCCCCCCCCCCC(C)OC3OC(CO)C(O)C(O)C3OC3OC(CO)C(O)C(O)C3OC2=O)OC1=O

InChI Identifier

InChI=1S/C33H56O14/c1-18-14-12-10-8-6-4-3-5-7-9-11-13-15-20-23(19(2)30(40)43-20)31(41)46-28-26(38)24(36)22(17-35)45-33(28)47-29-27(39)25(37)21(16-34)44-32(29)42-18/h18-29,32-39H,3-17H2,1-2H3

InChI Key

NFJPUMMCMMCPKZ-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
Pleopsidium gobiense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Disaccharide
Dicarboxylic acid or derivatives
Gamma butyrolactone
Oxane
Tetrahydrofuran
Carboxylic acid ester
Lactone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Polyol
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Primary 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	2.05	ALOGPS
logP	2.45	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	12.4	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	210.9 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	162.81 m³·mol⁻¹	ChemAxon
Polarizability	71.93 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

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 6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione (NP0240227)

MOL for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)

3D MOL for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)

3D SDF for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)

3D-SDF for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)

PDB for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)

3D PDB for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)

SMILES for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)

INCHI for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)

Structure for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)

3D Structure for NP0240227 (6,7,34,35-tetrahydroxy-5,33-bis(hydroxymethyl)-12,29-dimethyl-2,4,9,14,30,32-hexaoxatetracyclo[29.4.0.0³,⁸.0¹¹,¹⁵]pentatriacontane-10,13-dione)