NP-MRD: Showing NP-Card for 7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate (NP0271904)

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Record Information

Version

2.0

Created at

2022-09-08 18:20:24 UTC

Updated at

2022-09-08 18:20:24 UTC

NP-MRD ID

NP0271904

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate

Description

7-{1,2,9,14,18,18-Hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-6-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate belongs to the class of organic compounds known as bacteriohopanoids. These are bacterial terpenoids structurally characterized by a C30 skeleton, which is usually conjugated to a C5 (usually hydroxylated) unit linked by a carbon-carbon bond. Based on a literature review very few articles have been published on 7-{1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-6-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082220202D          

 48 53  0  0  0  0            999 V2000
    0.8400   -5.0922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8400   -5.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2690   -5.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9835   -6.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9835   -7.1547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6979   -5.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6979   -5.0922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4124   -6.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4124   -7.1547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8413   -6.3297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5558   -5.0922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6281   -5.9941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5391   -7.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.4080   -5.9211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1531   -6.7057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9601   -6.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7670   -6.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0220   -5.5781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4699   -4.9650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1696   -4.5278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1609   -4.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6630   -5.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1109   -4.5234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3040   -4.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0490   -5.4795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9628   -4.6591    0.0000 C   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
  5  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
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 13 14  2  0  0  0  0
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 17 18  1  0  0  0  0
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 19 20  1  0  0  0  0
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 16 21  1  0  0  0  0
  2 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
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 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
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 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 25 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
 35 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
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 41 44  1  0  0  0  0
 36 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 35 47  1  0  0  0  0
 30 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END

     RDKit          3D

116121  0  0  0  0  0  0  0  0999 V2000
    2.6153   -4.0150    0.4875 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6226   -3.0775   -0.1718 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4164   -2.2244   -1.1281 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5083   -1.4180   -0.4509 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1944   -0.6117   -1.5230 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7379   -1.4700   -2.4951 O   0  0  0  0  0  0  0  0  0  0  0  0
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   13.7080    1.8487   -0.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8722   -2.2731    0.8352 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -2.6100   -1.5522   -2.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2080   -3.1885   -0.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4631   -2.1490   -1.8325 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
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 48 47  1  0
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 21 16  1  0
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 48116  1  6
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 46112  1  0
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 35 94  1  0
 37 95  1  0
 37 96  1  0
 37 97  1  0
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 38 99  1  0
 38100  1  0
 39101  1  1
 40102  1  0
 40103  1  0
 41104  1  0
 41105  1  0
 43106  1  0
 43107  1  0
 43108  1  0
M  END


  Mrv1652309082220202D          

 48 53  0  0  0  0            999 V2000
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    2.9835   -6.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6979   -5.0922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4124   -6.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4124   -7.1547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1269   -5.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8413   -6.3297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5558   -5.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5558   -5.0922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2703   -6.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9847   -5.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9847   -5.0922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6992   -4.6797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4137   -5.0922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4137   -5.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6992   -6.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1256   -6.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0393   -7.1502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676   -7.3217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801   -6.6072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6651   -7.2747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6281   -5.9941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8830   -5.2095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6900   -5.0380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2421   -5.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4970   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9871   -6.4357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5391   -7.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3461   -6.8773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6011   -6.0926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4080   -5.9211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1531   -6.7057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9601   -6.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7670   -6.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0220   -5.5781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4699   -4.9650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1696   -4.5278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1609   -4.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6630   -5.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1109   -4.5234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3040   -4.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0490   -5.4795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9628   -4.6591    0.0000 C   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
  5  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
  2 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
 25 27  1  0  0  0  0
 22 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
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 25 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
 35 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
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 41 44  1  0  0  0  0
 36 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 35 47  1  0  0  0  0
 30 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0271904

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCC(O)C(O)C(O)COC(=O)CC1=CC=CC=C1)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCCC(C)(C)C3CCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C43H68O5/c1-28(14-15-32(44)38(47)33(45)27-48-37(46)26-29-12-9-8-10-13-29)30-18-23-40(4)31(30)19-24-42(6)35(40)16-17-36-41(5)22-11-21-39(2,3)34(41)20-25-43(36,42)7/h8-10,12-13,28,30-36,38,44-45,47H,11,14-27H2,1-7H3

> <INCHI_KEY>
SKTGBAZAHKIYNS-UHFFFAOYSA-N

> <FORMULA>
C43H68O5

> <MOLECULAR_WEIGHT>
665.012

> <EXACT_MASS>
664.50667529

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
116

> <JCHEM_AVERAGE_POLARIZABILITY>
81.10080664914213

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-{1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-6-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate

> <JCHEM_LOGP>
8.863422476333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.172298631519805

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.90961995650937

> <JCHEM_PKA_STRONGEST_BASIC>
-3.182464673587175

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
192.50690000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
7-{1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-6-yl}-2,3,4-trihydroxyoctyl phenylacetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       1.568  -9.505   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.568 -11.045   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.902 -11.815   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.235 -11.045   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.569 -11.815   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.569 -13.355   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.903 -11.045   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.903  -9.505   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.236 -11.815   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.236 -13.355   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.570 -11.045   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.904 -11.815   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      12.238 -11.045   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.238  -9.505   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      13.571 -11.815   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.905 -11.045   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.905  -9.505   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.239  -8.735   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.572  -9.505   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.572 -11.045   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.239 -11.815   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.234 -11.815   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.073 -13.347   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.433 -13.667   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.203 -12.333   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.108 -13.579   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.172 -11.189   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.648  -9.724   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.155  -9.404   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.185 -10.549   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.661  -9.084   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.709 -12.013   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -4.740 -13.158   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -6.246 -12.838   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -6.722 -11.373   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -8.228 -11.053   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -7.752 -12.517   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -9.259 -12.197   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -10.765 -11.877   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -11.241 -10.412   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -10.211  -9.268   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0     -11.517  -8.452   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -9.634  -7.840   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -8.704  -9.588   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -7.674  -8.444   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -6.167  -8.764   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -5.692 -10.228   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -5.531  -8.697   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22    2   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   32                                             
CONECT   26   25                                                            
CONECT   27   25   22   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32   47                                             
CONECT   31   30                                                            
CONECT   32   30   25   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   47                                                  
CONECT   36   35   37   38   44                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43   44                                             
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44   41   36   45                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   35   30   48                                             
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  106    0
END

View in JSmol

Synonyms

Value	Source
7-{1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0,.0,.0,]henicosan-6-yl}-2,3,4-trihydroxyoctyl 2-phenylacetic acid	Generator

Chemical Formula

C₄₃H₆₈O₅

Average Mass

665.0120 Da

Monoisotopic Mass

664.50668 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(CCC(O)C(O)C(O)COC(=O)CC1=CC=CC=C1)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCCC(C)(C)C3CCC12C

InChI Identifier

InChI=1S/C43H68O5/c1-28(14-15-32(44)38(47)33(45)27-48-37(46)26-29-12-9-8-10-13-29)30-18-23-40(4)31(30)19-24-42(6)35(40)16-17-36-41(5)22-11-21-39(2,3)34(41)20-25-43(36,42)7/h8-10,12-13,28,30-36,38,44-45,47H,11,14-27H2,1-7H3

InChI Key

SKTGBAZAHKIYNS-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 bacteriohopanoids. These are bacterial terpenoids structurally characterized by a C30 skeleton, which is usually conjugated to a C5 (usually hydroxylated) unit linked by a carbon-carbon bond.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Hopanoids

Direct Parent

Bacteriohopanoids

Alternative Parents

Substituents

Sesquaterpenoid
Bacteriohopane skeleton
27-hydroxysteroid
25-hydroxysteroid
24-hydroxysteroid
Steroid
Fatty alcohol ester
Fatty alcohol
Fatty acyl
Benzenoid
Monosaccharide
Monocyclic benzene moiety
Secondary alcohol
Carboxylic acid ester
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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

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

163062760

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate (NP0271904)

MOL for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)

3D MOL for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)

3D SDF for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)

3D-SDF for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)

PDB for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)

3D PDB for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)

SMILES for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)

INCHI for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)

Structure for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)

3D Structure for NP0271904 (7-{5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}-2,3,4-trihydroxyoctyl 2-phenylacetate)