NP-MRD: Showing NP-Card for (2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate (NP0319136)

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Record Information

Version

2.0

Created at

2022-09-11 20:01:07 UTC

Updated at

2022-09-11 20:01:08 UTC

NP-MRD ID

NP0319136

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate

Description

(2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate is found in Isodon lophanthoides.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112222012D          

 30 32  0  0  1  0            999 V2000
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3882   -1.0180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3276   -1.0180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 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
 15 17  2  0  0  0  0
 10 18  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  2  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 28 25  1  6  0  0  0
 20 28  1  0  0  0  0
 28 29  1  0  0  0  0
  3 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END

     RDKit          3D

 62 64  0  0  0  0  0  0  0  0999 V2000
   -0.2850   -2.9403    2.5803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5894   -2.3953    1.3633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9179   -1.0433    1.3935 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0167   -0.2587    0.5062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3713    0.8321   -0.1645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5290    1.5951   -1.0105 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2182    2.6314   -1.6521 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9066    1.1389   -1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8088    1.8303   -1.9330 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276    0.0482   -0.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7472   -0.3757   -0.6680 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8226   -1.7397   -1.3299 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4668   -0.3650    0.6562 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8114   -0.7616    0.5153 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7609   -0.1378   -0.2396 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1362   -0.7201   -0.2589 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4535    0.8869   -0.8817 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3959   -0.6845    0.3430 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7930   -1.7199    0.9528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7762    1.2611   -0.0422 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8920    1.9210    1.3295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2288    2.3164   -0.9967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6966    2.5925   -0.9342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5725    1.5184   -0.4155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9812    0.1425   -0.5948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1526   -0.1580   -2.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9433   -0.8260    0.0722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5824   -0.0128   -0.1574 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3820   -0.8894    1.0506 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0392   -0.4229    2.1787 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5365   -2.5222    3.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2150   -2.8765    3.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1747   -4.0485    2.4192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7375   -0.7650    2.4733 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9899    1.4379   -2.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2566    0.3255   -1.3368 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8014   -1.5918   -2.4227 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7898   -2.1811   -1.0508 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9443   -2.3468   -1.0654 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9302   -0.9767    1.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5117    0.7066    1.0179 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4390   -1.0805    0.7493 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1569   -1.5597   -0.9741 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8912    0.0205   -0.6073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5259    2.9938    1.2675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2650    1.4790    2.1014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8970    2.0037    1.7150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9656    2.1824   -2.0337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7372    3.2662   -0.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0822    2.8877   -1.9596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9371    3.5211   -0.3276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5331    1.4936   -1.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9623    1.6849    0.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4746    0.4655   -2.7032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9274   -1.2286   -2.2278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2175    0.0770   -2.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9330   -0.7289   -0.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6375   -1.8832   -0.0980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1177   -0.5870    1.1397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0721   -0.5948   -0.9915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8060   -1.8886    0.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7796   -0.9495    2.9586 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 29  1  0
 29 30  1  0
 29 28  1  0
 28 25  1  0
 25 26  1  0
 25 27  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  1  1
 20  5  1  0
  5  4  2  0
  4 18  1  0
 18 19  2  0
 18 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 10  8  2  0
  8  9  1  0
  8  6  1  0
  6  7  2  0
  4  3  1  0
 20 28  1  0
  6  5  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  1
 29 61  1  6
 30 62  1  0
 28 60  1  6
 26 54  1  0
 26 55  1  0
 26 56  1  0
 27 57  1  0
 27 58  1  0
 27 59  1  0
 24 52  1  0
 24 53  1  0
 23 50  1  0
 23 51  1  0
 22 48  1  0
 22 49  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
 11 36  1  6
 12 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
  9 35  1  0
M  END


  Mrv1652309112222012D          

 30 32  0  0  1  0            999 V2000
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3882   -1.0180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3276   -1.0180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 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
 15 17  2  0  0  0  0
 10 18  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  2  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 28 25  1  6  0  0  0
 20 28  1  0  0  0  0
 28 29  1  0  0  0  0
  3 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0319136

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1[C@@H](O)[C@H]2C(C)(C)CCC[C@]2(C)C2=C1C(=O)C([C@H](C)COC(C)=O)=C(O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O7/c1-11(10-30-12(2)24)13-16(25)14-15(18(27)17(13)26)23(5)9-7-8-22(3,4)21(23)19(28)20(14)29-6/h11,19-21,26,28H,7-10H2,1-6H3/t11-,19-,20+,21+,23-/m1/s1

> <INCHI_KEY>
BFNZTROYCRMMRA-HCDGCQJGSA-N

> <FORMULA>
C23H32O7

> <MOLECULAR_WEIGHT>
420.502

> <EXACT_MASS>
420.21480337

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.81600403308202

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-[(4bS,8aS,9S,10S)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-1,4,4b,5,6,7,8,8a,9,10-decahydrophenanthren-2-yl]propyl acetate

> <JCHEM_LOGP>
2.2334358263333325

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.837804302178103

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.860591419874458

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3142244156284493

> <JCHEM_POLAR_SURFACE_AREA>
110.13000000000001

> <JCHEM_REFRACTIVITY>
111.16709999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(4bS,8aS,9S,10S)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.001  -8.470   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.001  -8.470   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335  -6.160   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.668  -3.850   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.325  -1.900   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.345  -1.900   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -2.667  -1.540   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5   18                                                  
CONECT    5    4    6   20                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   18                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   10    4   19                                                  
CONECT   19   18                                                            
CONECT   20    5   21   22   28                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   20   29                                                  
CONECT   29   28    3   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₇

Average Mass

420.5020 Da

Monoisotopic Mass

420.21480 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CO[C@@H]1[C@@H](O)[C@H]2C(C)(C)CCC[C@]2(C)C2=C1C(=O)C([C@H](C)COC(C)=O)=C(O)C2=O

InChI Identifier

InChI=1S/C23H32O7/c1-11(10-30-12(2)24)13-16(25)14-15(18(27)17(13)26)23(5)9-7-8-22(3,4)21(23)19(28)20(14)29-6/h11,19-21,26,28H,7-10H2,1-6H3/t11-,19-,20+,21+,23-/m1/s1

InChI Key

BFNZTROYCRMMRA-HCDGCQJGSA-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
Isodon lophanthoides	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate (NP0319136)

MOL for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)

3D MOL for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)

3D SDF for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)

3D-SDF for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)

PDB for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)

3D PDB for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)

SMILES for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)

INCHI for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)

Structure for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)

3D Structure for NP0319136 ((2s)-2-[(4bs,8as,9s,10s)-3,9-dihydroxy-10-methoxy-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate)