NP-MRD: Showing NP-Card for 6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate (NP0183231)

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Record Information

Version

2.0

Created at

2022-09-03 22:06:01 UTC

Updated at

2022-09-03 22:06:01 UTC

NP-MRD ID

NP0183231

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate

Description

6,9-Bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]Octadec-1(18)-en-17-yl acetate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate is found in Astragalus membranaceus. 6,9-Bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]Octadec-1(18)-en-17-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231518172D          

 56 60  0  0  0  0            999 V2000
   -0.8132   -3.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9321   -2.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6986   -2.6322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3461   -3.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126   -2.8382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2316   -2.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5841   -1.5106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9981   -1.7166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1170   -0.9003    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8835   -0.5951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5310   -1.1063    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2975   -0.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9450   -1.3123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7115   -1.0072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4165    0.0153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1829    0.3204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7689    0.5265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8879    1.3428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0024    0.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3549    0.7325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2846   -2.4261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3176   -1.6018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0039   -1.1439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4562   -1.3157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9674   -1.9632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3511   -1.2329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7907   -2.0166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1412   -1.2698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9436   -1.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1191   -0.2720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5087    0.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7229    0.0320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6842    1.0892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5938   -1.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3040   -1.1663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7674   -0.5397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8280   -0.5290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0226   -1.5716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -2.3966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3206   -2.8162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6720   -3.2330    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9622   -2.9318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561   -2.7563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6983   -3.4426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8750   -3.3892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4171   -4.0755    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7825   -4.8151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6058   -4.8685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3247   -5.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5096   -2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0175   -3.2842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7329   -1.1520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4515   -1.5573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1618   -1.1376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4598   -2.3822    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
  5  4  1  4  0  0  0
  5  6  2  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
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 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
 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
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 35 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
 34 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 27 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 46 51  1  0  0  0  0
 21 51  1  0  0  0  0
 25 51  1  0  0  0  0
 51 52  1  0  0  0  0
 38 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 54 56  1  0  0  0  0
M  END

     RDKit          3D

122126  0  0  0  0  0  0  0  0999 V2000
  -10.1962    3.3371    3.3735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8558    2.7406    3.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8483    3.2120    3.7481 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6595    1.6988    2.2751 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3802    1.0895    2.0119 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.5091   -0.3261    2.4417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5426   -1.2904    1.8382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2662   -1.0929    0.3818 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.4460   -1.6019   -0.2518 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1705   -1.9635   -0.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7805   -1.5511    0.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0709   -2.1856   -0.8515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5945   -2.0596   -1.0436 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1704   -3.4402   -1.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7474   -4.0789   -2.1963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3086   -5.5224   -2.1696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7216   -3.4607   -3.2846 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8718   -1.3484    0.0272 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3805   -2.4936    0.9986 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3261   -0.6129   -0.3642 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9803   -0.8340   -1.6903 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2589   -0.1871   -2.8473 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3553   -0.2166   -1.6552 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2933   -0.6865   -0.6166 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8323   -1.9315   -1.1957 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9142    0.3706   -1.3543 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.4504    1.0332    1.0795 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1352    2.1790    1.4350 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4740    0.8130   -0.4384 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.3544    2.0526   -1.0478 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2526   -0.0657   -0.7374 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.3239   -0.4190   -2.0694 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1748    0.8159   -0.0137 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0450    1.2439    1.0137 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6864   -0.4169    0.8720 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0893   -0.5118    2.2942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1250   -0.6371    1.0075 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9429    0.6434    1.0406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7496    0.8298   -0.1848 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1633    0.3028   -1.3756 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.5015    1.1405   -0.1339 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3667    3.5775    4.4327 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2255    4.2774    2.7635 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9799    2.6751    2.9479 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.5654   -0.6891    2.3284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0412   -2.3077    1.9421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6389   -1.4271    2.4771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2058   -1.7358   -1.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3727   -2.2921   -1.1306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2608   -2.9467    0.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5651   -2.8738   -1.5619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4848   -1.6050   -2.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1108   -5.8092   -3.1433 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4233   -5.5941   -1.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2030   -6.1230   -1.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2394   -3.0095    1.4288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3736   -2.1123    1.6811 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1511   -0.9809    0.3686 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0128   -0.5452    0.4337 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.6765    1.4661   -1.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


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M  END
> <DATABASE_ID>
NP0183231

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCC=C(C)COC1OC(CO)C(O)C(O)C1O)C1C(O)CC2(C)C3CC(OC(C)=O)C4C(C)(C)C(CCC4(O)CC3=CC(OC(C)=O)C12C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C42H66O14/c1-21(20-52-38-36(50)35(49)34(48)30(19-43)56-38)11-10-12-22(2)33-28(47)18-40(8)27-16-29(53-23(3)44)37-39(6,7)31(54-24(4)45)13-14-42(37,51)17-26(27)15-32(41(33,40)9)55-25(5)46/h11,15,22,27-38,43,47-51H,10,12-14,16-20H2,1-9H3

> <INCHI_KEY>
WWRVOMJIBFKDOV-UHFFFAOYSA-N

> <FORMULA>
C42H66O14

> <MOLECULAR_WEIGHT>
794.976

> <EXACT_MASS>
794.445256805

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
122

> <JCHEM_AVERAGE_POLARIZABILITY>
87.48806426524483

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate

> <ALOGPS_LOGP>
2.71

> <JCHEM_LOGP>
1.2005376203333358

> <ALOGPS_LOGS>
-4.15

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.167217575985543

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.206605655148179

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8426012165765977

> <JCHEM_POLAR_SURFACE_AREA>
218.73999999999995

> <JCHEM_REFRACTIVITY>
202.70950000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.64e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      -1.518  -7.007   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.740  -5.483   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.171  -4.913   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.379  -5.868   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.810  -5.298   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.032  -3.774   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.824  -2.820   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.463  -3.204   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -7.685  -1.681   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -9.116  -1.111   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0     -10.325  -2.065   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0     -11.755  -1.495   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -12.964  -2.450   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0     -14.395  -1.880   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0     -11.977   0.028   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0     -13.408   0.598   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0     -10.769   0.983   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0     -10.991   2.507   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -9.338   0.413   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -8.129   1.367   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.531  -4.529   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.593  -2.990   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.874  -2.135   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.852  -2.456   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.806  -3.665   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.522  -2.301   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.343  -3.764   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.997  -2.370   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.495  -2.012   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.822  -0.508   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.683   0.528   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.216   0.060   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.011   2.033   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.708  -2.961   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.034  -2.177   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.033  -1.007   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.012  -0.988   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.376  -2.934   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.391  -4.474   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.065  -5.257   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.724  -4.500   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       6.854  -6.035   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       5.530  -5.473   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.025  -5.145   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.170  -6.426   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       1.633  -6.326   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       0.779  -7.608   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       1.461  -8.988   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       2.997  -9.088   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       0.606 -10.269   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       0.951  -4.946   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -0.033  -6.130   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      10.701  -2.150   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      12.043  -2.907   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      13.369  -2.124   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      12.058  -4.447   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   10   20                                                  
CONECT   20   19                                                            
CONECT   21    2   22   51                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27   51                                             
CONECT   26   25                                                            
CONECT   27   25   28   44                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   29   35   41                                                  
CONECT   35   34   36   37   38                                             
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   35   39   53                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   34   42   43                                             
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   27   45                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47   51                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48                                                            
CONECT   51   46   21   25   52                                             
CONECT   52   51                                                            
CONECT   53   38   54                                                       
CONECT   54   53   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  120    0
END

View in JSmol

Synonyms

Value	Source
6,9-Bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0,.0,]octadec-1(18)-en-17-yl acetic acid	Generator
6,9-Bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetic acid	Generator

Chemical Formula

C₄₂H₆₆O₁₄

Average Mass

794.9760 Da

Monoisotopic Mass

794.44526 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(CCC=C(C)COC1OC(CO)C(O)C(O)C1O)C1C(O)CC2(C)C3CC(OC(C)=O)C4C(C)(C)C(CCC4(O)CC3=CC(OC(C)=O)C12C)OC(C)=O

InChI Identifier

InChI=1S/C42H66O14/c1-21(20-52-38-36(50)35(49)34(48)30(19-43)56-38)11-10-12-22(2)33-28(47)18-40(8)27-16-29(53-23(3)44)37-39(6,7)31(54-24(4)45)13-14-42(37,51)17-26(27)15-32(41(33,40)9)55-25(5)46/h11,15,22,27-38,43,47-51H,10,12-14,16-20H2,1-9H3

InChI Key

WWRVOMJIBFKDOV-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
Astragalus membranaceus	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
Steroid
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Tricarboxylic acid or derivatives
Fatty acyl
Monosaccharide
Oxane
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Polyol
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
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	2.71	ALOGPS
logP	1.2	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	218.74 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	202.71 m³·mol⁻¹	ChemAxon
Polarizability	87.49 Å³	ChemAxon
Number of Rings	5	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 6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate (NP0183231)

MOL for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)

3D MOL for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)

3D SDF for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)

3D-SDF for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)

PDB for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)

3D PDB for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)

SMILES for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)

INCHI for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)

Structure for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)

3D Structure for NP0183231 (6,9-bis(acetyloxy)-3,14-dihydroxy-7,7,12,16-tetramethyl-15-(6-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hept-5-en-2-yl)tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadec-1(18)-en-17-yl acetate)