NP-MRD: Showing NP-Card for 15-acetoxy-7-oxodehydroabietic acid (NP0027163)

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Record Information

Version

2.0

Created at

2021-06-19 18:51:42 UTC

Updated at

2021-06-29 23:53:07 UTC

NP-MRD ID

NP0027163

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-acetoxy-7-oxodehydroabietic acid

Provided By

JEOL Database JEOL Logo

Description

15-acetoxy-7-oxodehydroabietic acid is found in Picea morrisonicola. 15-acetoxy-7-oxodehydroabietic acid was first documented in 2004 (Kuo, Y.-H., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192120513D          

 55 57  0  0  0  0            999 V2000
   -4.2901   -5.2040    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9558   -5.1996    1.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3870   -6.2067    1.5216 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5039   -3.9252    1.2322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2295   -3.6123    1.8607 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0850   -4.2732    1.0728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2494   -4.0562    3.3339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0570   -2.0794    1.8042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0900   -1.4613    2.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2599   -0.0714    2.2805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7025    0.7652    1.6963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8605    0.1536    1.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0312   -1.2419    1.2396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9451    0.9603    0.5640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0284    0.4414    0.3007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7021    2.4274    0.2942 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2303    2.8669    0.3817 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5549    2.2875    1.6707 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2695    2.8139    2.9469 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9000    2.8237    1.7502 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7264    2.5406    0.5065 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0704    3.1385   -0.7309 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3994    2.6900   -0.9489 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9568    3.6128   -2.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3948    1.2588   -1.4996 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5242    0.4582   -1.4635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5612    0.8994   -2.0666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0085   -4.6255    1.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6535   -6.2325    0.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1925   -4.7902   -0.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1502   -5.3650    1.0902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1198   -3.9755    0.0179 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9013   -4.0089    1.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1037   -3.6130    3.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3368   -3.7712    3.8678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3494   -5.1406    3.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8791   -2.0560    2.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.9465   -1.6664    0.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1306    2.6666   -0.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2944    2.9831    1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3002    2.4544    3.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7447    2.4878    3.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2991    3.9095    2.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8693    3.9142    1.8890 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9810    3.3610   -2.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4245   -0.0310   -2.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0  0  0  0
 13  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 22 23  1  0  0  0  0
 14 15  2  0  0  0  0
 18 11  1  0  0  0  0
  8  5  1  0  0  0  0
 17 16  1  0  0  0  0
  5  6  1  0  0  0  0
 16 14  1  0  0  0  0
  5  7  1  0  0  0  0
 14 12  1  0  0  0  0
  5  4  1  6  0  0  0
 11 12  2  0  0  0  0
  4  2  1  0  0  0  0
 23 17  1  0  0  0  0
  2  1  1  0  0  0  0
 18 20  1  0  0  0  0
  2  3  2  0  0  0  0
 18 17  1  0  0  0  0
 18 19  1  1  0  0  0
 23 24  1  0  0  0  0
 21 22  1  0  0  0  0
 23 25  1  6  0  0  0
 21 20  1  0  0  0  0
 25 26  2  0  0  0  0
 11 10  1  0  0  0  0
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 21 48  1  0  0  0  0
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 13 39  1  0  0  0  0
  9 37  1  0  0  0  0
 10 38  1  0  0  0  0
  6 31  1  0  0  0  0
  6 32  1  0  0  0  0
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  1 28  1  0  0  0  0
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 24 52  1  0  0  0  0
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 27 55  1  0  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
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   -1.2494   -4.0562    3.3339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0570   -2.0794    1.8042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0900   -1.4613    2.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2599   -0.0714    2.2805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7025    0.7652    1.6963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8605    0.1536    1.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0312   -1.2419    1.2396 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2303    2.8669    0.3817 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.3948    1.2588   -1.4996 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306192120513D          

 55 57  0  0  0  0            999 V2000
   -4.2901   -5.2040    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9558   -5.1996    1.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3870   -6.2067    1.5216 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5039   -3.9252    1.2322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2295   -3.6123    1.8607 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -2.9465   -1.6664    0.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1306    2.6666   -0.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2944    2.9831    1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2701    3.9584    0.5307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3002    2.4544    3.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7447    2.4878    3.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2991    3.9095    2.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4256    2.4410    2.6325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8693    3.9142    1.8890 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7224    2.9828    0.6292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8853    1.4652    0.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6822    2.8913   -1.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1060    4.2325   -0.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9543    4.6623   -1.7491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3476    3.5367   -2.9737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9810    3.3610   -2.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4245   -0.0310   -2.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0  0  0  0
 13  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 22 23  1  0  0  0  0
 14 15  2  0  0  0  0
 18 11  1  0  0  0  0
  8  5  1  0  0  0  0
 17 16  1  0  0  0  0
  5  6  1  0  0  0  0
 16 14  1  0  0  0  0
  5  7  1  0  0  0  0
 14 12  1  0  0  0  0
  5  4  1  6  0  0  0
 11 12  2  0  0  0  0
  4  2  1  0  0  0  0
 23 17  1  0  0  0  0
  2  1  1  0  0  0  0
 18 20  1  0  0  0  0
  2  3  2  0  0  0  0
 18 17  1  0  0  0  0
 18 19  1  1  0  0  0
 23 24  1  0  0  0  0
 21 22  1  0  0  0  0
 23 25  1  6  0  0  0
 21 20  1  0  0  0  0
 25 26  2  0  0  0  0
 11 10  1  0  0  0  0
 25 27  1  0  0  0  0
 21 48  1  0  0  0  0
 21 49  1  0  0  0  0
 22 50  1  0  0  0  0
 22 51  1  0  0  0  0
 20 46  1  0  0  0  0
 20 47  1  0  0  0  0
 17 42  1  1  0  0  0
 16 40  1  0  0  0  0
 16 41  1  0  0  0  0
 13 39  1  0  0  0  0
  9 37  1  0  0  0  0
 10 38  1  0  0  0  0
  6 31  1  0  0  0  0
  6 32  1  0  0  0  0
  6 33  1  0  0  0  0
  7 34  1  0  0  0  0
  7 35  1  0  0  0  0
  7 36  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
 19 43  1  0  0  0  0
 19 44  1  0  0  0  0
 19 45  1  0  0  0  0
 24 52  1  0  0  0  0
 24 53  1  0  0  0  0
 24 54  1  0  0  0  0
 27 55  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0027163

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)[C@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@@]2(C3=C(C([H])=C(C([H])=C3[H])C(OC(=O)C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C(=O)C([H])([H])[C@]12[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O5/c1-13(23)27-20(2,3)14-7-8-16-15(11-14)17(24)12-18-21(16,4)9-6-10-22(18,5)19(25)26/h7-8,11,18H,6,9-10,12H2,1-5H3,(H,25,26)/t18-,21+,22+/m0/s1

> <INCHI_KEY>
MVSNOMINTBGJOH-VLCRHTCISA-N

> <FORMULA>
C22H28O5

> <MOLECULAR_WEIGHT>
372.461

> <EXACT_MASS>
372.193674002

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
40.04674457462755

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4aS,10aS)-7-[2-(acetyloxy)propan-2-yl]-1,4a-dimethyl-9-oxo-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid

> <ALOGPS_LOGP>
4.06

> <JCHEM_LOGP>
3.7303075596666657

> <ALOGPS_LOGS>
-5.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
15.883655578643246

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9310981790259736

> <JCHEM_PKA_STRONGEST_BASIC>
-6.8921451650638454

> <JCHEM_POLAR_SURFACE_AREA>
80.67

> <JCHEM_REFRACTIVITY>
101.0641

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.51e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4aS,10aS)-7-[2-(acetyloxy)propan-2-yl]-1,4a-dimethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
   -4.2901   -5.2040    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9558   -5.1996    1.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3870   -6.2067    1.5216 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5039   -3.9252    1.2322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2295   -3.6123    1.8607 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0850   -4.2732    1.0728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2494   -4.0562    3.3339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0570   -2.0794    1.8042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0900   -1.4613    2.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2599   -0.0714    2.2805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7025    0.7652    1.6963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8605    0.1536    1.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0312   -1.2419    1.2396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9451    0.9603    0.5640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0284    0.4414    0.3007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7021    2.4274    0.2942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2303    2.8669    0.3817 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5549    2.2875    1.6707 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2695    2.8139    2.9469 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9000    2.8237    1.7502 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7264    2.5406    0.5065 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0704    3.1385   -0.7309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3994    2.6900   -0.9489 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9568    3.6128   -2.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3948    1.2588   -1.4996 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5242    0.4582   -1.4635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5612    0.8994   -2.0666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0085   -4.6255    1.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6535   -6.2325    0.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1925   -4.7902   -0.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1502   -5.3650    1.0902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1198   -3.9755    0.0179 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9013   -4.0089    1.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1037   -3.6130    3.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3368   -3.7712    3.8678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3494   -5.1406    3.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8791   -2.0560    2.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1692    0.3309    2.7189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9465   -1.6664    0.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1306    2.6666   -0.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2944    2.9831    1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2701    3.9584    0.5307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3002    2.4544    3.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7447    2.4878    3.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2991    3.9095    2.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4256    2.4410    2.6325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8693    3.9142    1.8890 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7224    2.9828    0.6292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8853    1.4652    0.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6822    2.8913   -1.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1060    4.2325   -0.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9543    4.6623   -1.7491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3476    3.5367   -2.9737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9810    3.3610   -2.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4245   -0.0310   -2.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0
 13  8  2  0
  8  9  1  0
  9 10  2  0
 22 23  1  0
 14 15  2  0
 18 11  1  0
  8  5  1  0
 17 16  1  0
  5  6  1  0
 16 14  1  0
  5  7  1  0
 14 12  1  0
  5  4  1  6
 11 12  2  0
  4  2  1  0
 23 17  1  0
  2  1  1  0
 18 20  1  0
  2  3  2  0
 18 17  1  0
 18 19  1  1
 23 24  1  0
 21 22  1  0
 23 25  1  6
 21 20  1  0
 25 26  2  0
 11 10  1  0
 25 27  1  0
 21 48  1  0
 21 49  1  0
 22 50  1  0
 22 51  1  0
 20 46  1  0
 20 47  1  0
 17 42  1  1
 16 40  1  0
 16 41  1  0
 13 39  1  0
  9 37  1  0
 10 38  1  0
  6 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 24 52  1  0
 24 53  1  0
 24 54  1  0
 27 55  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.290  -5.204   0.447  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.956  -5.200   1.129  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.387  -6.207   1.522  0.00  0.00           O+0
HETATM    4  O   UNK     0      -2.504  -3.925   1.232  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.230  -3.612   1.861  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.085  -4.273   1.073  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.249  -4.056   3.334  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.057  -2.079   1.804  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.090  -1.461   2.325  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.260  -0.071   2.281  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.703   0.765   1.696  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.861   0.154   1.185  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.031  -1.242   1.240  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.945   0.960   0.564  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.028   0.441   0.301  0.00  0.00           O+0
HETATM   16  C   UNK     0      -2.702   2.427   0.294  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.230   2.867   0.382  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.555   2.288   1.671  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.270   2.814   2.947  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.900   2.824   1.750  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.726   2.541   0.506  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.070   3.139  -0.731  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.399   2.690  -0.949  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.957   3.613  -2.065  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.395   1.259  -1.500  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.524   0.458  -1.464  0.00  0.00           O+0
HETATM   27  O   UNK     0      -1.561   0.899  -2.067  0.00  0.00           O+0
HETATM   28  H   UNK     0      -5.008  -4.625   1.033  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.654  -6.232   0.367  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.192  -4.790  -0.560  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.150  -5.365   1.090  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.120  -3.975   0.018  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.901  -4.009   1.468  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.104  -3.613   3.860  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.337  -3.771   3.868  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.349  -5.141   3.436  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.879  -2.056   2.783  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.169   0.331   2.719  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.946  -1.666   0.830  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.131   2.667  -0.683  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.294   2.983   1.032  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.270   3.958   0.531  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.300   2.454   3.037  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.745   2.488   3.854  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.299   3.910   2.959  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.426   2.441   2.632  0.00  0.00           H+0
HETATM   47  H   UNK     0       0.869   3.914   1.889  0.00  0.00           H+0
HETATM   48  H   UNK     0       2.722   2.983   0.629  0.00  0.00           H+0
HETATM   49  H   UNK     0       1.885   1.465   0.385  0.00  0.00           H+0
HETATM   50  H   UNK     0       1.682   2.891  -1.608  0.00  0.00           H+0
HETATM   51  H   UNK     0       1.106   4.232  -0.634  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.954   4.662  -1.749  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.348   3.537  -2.974  0.00  0.00           H+0
HETATM   54  H   UNK     0      -1.981   3.361  -2.355  0.00  0.00           H+0
HETATM   55  H   UNK     0      -1.425  -0.031  -2.346  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    4    1    3                                                  
CONECT    3    2                                                            
CONECT    4    5    2                                                       
CONECT    5    8    6    7    4                                             
CONECT    6    5   31   32   33                                             
CONECT    7    5   34   35   36                                             
CONECT    8   13    9    5                                                  
CONECT    9    8   10   37                                                  
CONECT   10    9   11   38                                                  
CONECT   11   18   12   10                                                  
CONECT   12   13   14   11                                                  
CONECT   13   12    8   39                                                  
CONECT   14   15   16   12                                                  
CONECT   15   14                                                            
CONECT   16   17   14   40   41                                             
CONECT   17   16   23   18   42                                             
CONECT   18   11   20   17   19                                             
CONECT   19   18   43   44   45                                             
CONECT   20   18   21   46   47                                             
CONECT   21   22   20   48   49                                             
CONECT   22   23   21   50   51                                             
CONECT   23   22   17   24   25                                             
CONECT   24   23   52   53   54                                             
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   55                                                       
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    6                                                            
CONECT   32    6                                                            
CONECT   33    6                                                            
CONECT   34    7                                                            
CONECT   35    7                                                            
CONECT   36    7                                                            
CONECT   37    9                                                            
CONECT   38   10                                                            
CONECT   39   13                                                            
CONECT   40   16                                                            
CONECT   41   16                                                            
CONECT   42   17                                                            
CONECT   43   19                                                            
CONECT   44   19                                                            
CONECT   45   19                                                            
CONECT   46   20                                                            
CONECT   47   20                                                            
CONECT   48   21                                                            
CONECT   49   21                                                            
CONECT   50   22                                                            
CONECT   51   22                                                            
CONECT   52   24                                                            
CONECT   53   24                                                            
CONECT   54   24                                                            
CONECT   55   27                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  114    0
END

RDKit          3D

55 57  0  0  0  0  0  0  0  0999 V2000
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   -5.0085   -4.6255    1.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1925   -4.7902   -0.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2991    3.9095    2.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4256    2.4410    2.6325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8693    3.9142    1.8890 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7224    2.9828    0.6292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8853    1.4652    0.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6822    2.8913   -1.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1060    4.2325   -0.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9543    4.6623   -1.7491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3476    3.5367   -2.9737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9810    3.3610   -2.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4245   -0.0310   -2.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
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 22 23  1  0
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 18 11  1  0
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 17 16  1  0
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  2  1  1  0
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 11 10  1  0
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 17 42  1  1
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 13 39  1  0
  9 37  1  0
 10 38  1  0
  6 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 24 52  1  0
 24 53  1  0
 24 54  1  0
 27 55  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₈O₅

Average Mass

372.4610 Da

Monoisotopic Mass

372.19367 Da

IUPAC Name

(1R,4aS,10aS)-7-[2-(acetyloxy)propan-2-yl]-1,4a-dimethyl-9-oxo-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid

Traditional Name

(1R,4aS,10aS)-7-[2-(acetyloxy)propan-2-yl]-1,4a-dimethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

[H]OC(=O)[C@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@@]2(C3=C(C([H])=C(C([H])=C3[H])C(OC(=O)C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C(=O)C([H])([H])[C@]12[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C22H28O5/c1-13(23)27-20(2,3)14-7-8-16-15(11-14)17(24)12-18-21(16,4)9-6-10-22(18,5)19(25)26/h7-8,11,18H,6,9-10,12H2,1-5H3,(H,25,26)/t18-,21+,22+/m0/s1

InChI Key

MVSNOMINTBGJOH-VLCRHTCISA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Picea morrisonicola	JEOL database	Kuo, Y.-H., et al, Chem. Pharm. Bull. 52, 861 (2004)

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
logP	4.06	ALOGPS
logP	3.73	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	3.93	ChemAxon
pKa (Strongest Basic)	-6.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	80.67 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	101.06 m³·mol⁻¹	ChemAxon
Polarizability	40.05 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Kuo, Y.-H., et al. (2004). Kuo, Y.-H., et al, Chem. Pharm. Bull. 52, 861 (2004). Chem. Pharm. Bull..

Showing NP-Card for 15-acetoxy-7-oxodehydroabietic acid (NP0027163)

MOL for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)

3D MOL for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)

3D SDF for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)

3D-SDF for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)

PDB for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)

3D PDB for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)

SMILES for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)

INCHI for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)

Structure for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)

3D Structure for NP0027163 (15-acetoxy-7-oxodehydroabietic acid)