NP-MRD: Showing NP-Card for (3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid (NP0251111)

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Record Information

Version

2.0

Created at

2022-09-07 14:12:25 UTC

Updated at

2022-09-07 14:12:25 UTC

NP-MRD ID

NP0251111

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid

Description

Caesaljapin C belongs to the class of organic compounds known as steroid acids. Steroid acids are compounds containing a carboxyl group attached to a steroid backbone. Based on a literature review very few articles have been published on Caesaljapin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072216122D          

 30 33  0  0  1  0            999 V2000
   -1.7270   -3.7504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9142   -3.6091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6302   -2.8345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1589   -2.2012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -2.6932    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1807   -3.5182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -1.9173    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9098   -1.7721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582   -0.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0022   -0.8509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266   -2.2077    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0584   -1.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8008   -1.2171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -2.3529    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8705   -1.7222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -1.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -1.3611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -1.8241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -2.6166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -2.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -3.2741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7114   -4.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -3.1289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0872   -3.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -3.6143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -2.8384    0.0000 C   0  0  1  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  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 20 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 30 29  1  1  0  0  0
 14 30  1  0  0  0  0
  5 30  1  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
    4.7223    1.7568    2.0590 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9698    1.2197    0.9880 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5589    1.1780    1.0454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0731    1.6398    2.0840 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7748    0.6180   -0.0721 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1793    1.5585   -1.2501 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3919   -0.7062   -0.5231 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7591   -0.6434   -0.2393 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7775   -0.6973   -1.1520 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2195   -0.6257   -0.7936 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4840   -0.8135   -2.3586 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6818   -1.8858    0.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2724   -1.8259   -0.5305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3907   -0.6907    0.2692 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4659   -1.1630    1.6378 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1053   -0.6756    2.6554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2388   -2.2791    1.9327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7991   -0.4882   -0.3193 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5098   -1.7286   -0.6424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9792   -1.6162   -0.5813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8820   -2.5485   -0.7718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0758   -2.0729   -0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9878   -0.7360   -0.3326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6407   -0.4617   -0.3026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8729    0.7661   -0.0410 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7606    1.6493   -1.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4991    0.4772    0.5610 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7790    1.7779    0.7376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2944    1.6493    0.9189 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3193    0.6040    0.0327 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5233    2.4537    1.6747 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1673    0.9514    2.6770 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0472    2.3907    2.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7797    1.0453   -2.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7215    2.5444   -1.1002 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2808    1.5854   -1.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2853   -0.8077   -1.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7284   -1.4874   -1.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3483   -0.7364    0.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6736    0.3087   -1.1601 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5482   -1.8315    1.1613 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1353   -2.7943   -0.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3577   -1.4726   -1.5630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2492   -2.7731   -0.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9797   -2.2361    2.6239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5843    0.0411   -1.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2400   -2.6414   -0.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2870   -2.0159   -1.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0297   -2.5820   -0.7277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7862   -0.0114   -0.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4050    1.3488    0.7673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5847    1.4671   -1.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8143    1.5829   -1.7918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8691    2.7366   -0.9545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7028   -0.0200    1.5347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2009    2.2725    1.6299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0018    2.4279   -0.1245 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1942    2.6109    0.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1002    1.4896    1.9985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0693    0.9164   -1.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  5  3  1  1
  5  6  1  0
  5  7  1  0
  7 12  1  0
 12 13  1  0
 13 14  1  0
 14 18  1  0
 18 19  1  0
 19 20  1  0
 20 24  2  0
 24 23  1  0
 23 22  2  0
 22 21  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 14 15  1  1
 15 17  1  0
 15 16  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 30  5  1  0
 30 14  1  0
 27 18  1  0
 21 20  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  6 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  6
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 18 46  1  6
 19 47  1  0
 19 48  1  0
 23 50  1  0
 22 49  1  0
 25 51  1  1
 26 52  1  0
 26 53  1  0
 26 54  1  0
 27 55  1  1
 28 56  1  0
 28 57  1  0
 29 58  1  0
 29 59  1  0
 30 60  1  6
 17 45  1  0
 10 38  1  0
 10 39  1  0
 10 40  1  0
M  END


  Mrv1652309072216122D          

 30 33  0  0  1  0            999 V2000
   -1.7270   -3.7504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9142   -3.6091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6302   -2.8345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1589   -2.2012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -2.6932    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1807   -3.5182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -1.9173    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9098   -1.7721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582   -0.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0022   -0.8509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266   -2.2077    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0584   -1.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8008   -1.2171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -2.3529    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8705   -1.7222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -1.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -1.3611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -1.8241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -2.6166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -2.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -3.2741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7114   -4.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -3.1289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0872   -3.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -3.6143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -2.8384    0.0000 C   0  0  1  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  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 20 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 30 29  1  1  0  0  0
 14 30  1  0  0  0  0
  5 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0251111

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]1(C)[C@H](CC[C@@]2([C@H]3CC4=C(C=CO4)[C@H](C)[C@@H]3CC[C@@H]12)C(O)=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O7/c1-12-14-5-6-18-22(3,21(27)28-4)19(30-13(2)24)7-9-23(18,20(25)26)16(14)11-17-15(12)8-10-29-17/h8,10,12,14,16,18-19H,5-7,9,11H2,1-4H3,(H,25,26)/t12-,14+,16+,18+,19+,22-,23+/m1/s1

> <INCHI_KEY>
RZUPNWIKIOESCU-GILHYWDNSA-N

> <FORMULA>
C23H30O7

> <MOLECULAR_WEIGHT>
418.486

> <EXACT_MASS>
418.199153306

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
44.275208984105305

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,5S,6R,7R,10S,11R)-5-(acetyloxy)-6-(methoxycarbonyl)-6,11-dimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-2-carboxylic acid

> <JCHEM_LOGP>
3.2424644760000003

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.595445072532941

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8153111547440757

> <JCHEM_POLAR_SURFACE_AREA>
103.04

> <JCHEM_REFRACTIVITY>
105.99699999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5S,6R,7R,10S,11R)-5-(acetyloxy)-6-(methoxycarbonyl)-6,11-dimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.224  -7.001   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.706  -6.737   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.176  -5.291   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.163  -4.109   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.341  -5.027   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.337  -6.567   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.182  -3.579   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.698  -3.308   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.221  -1.859   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.229  -0.682   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -3.737  -1.588   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.810  -2.402   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.326  -2.673   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.850  -4.121   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.842  -2.944   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.228  -2.272   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       3.319  -1.495   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.366  -4.392   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.358  -3.215   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.874  -3.486   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.090  -2.541   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.365  -3.405   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.937  -4.884   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.398  -4.934   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.405  -6.112   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.928  -7.560   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.889  -5.841   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.896  -7.018   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.380  -6.747   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.857  -5.298   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   30                                             
CONECT    6    5                                                            
CONECT    7    5    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   18   30                                             
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   14   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   18   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   14    5                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₀O₇

Average Mass

418.4860 Da

Monoisotopic Mass

418.19915 Da

IUPAC Name

(1S,2S,5S,6R,7R,10S,11R)-5-(acetyloxy)-6-(methoxycarbonyl)-6,11-dimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-2-carboxylic acid

Traditional Name

(1S,2S,5S,6R,7R,10S,11R)-5-(acetyloxy)-6-(methoxycarbonyl)-6,11-dimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@]1(C)[C@H](CC[C@@]2([C@H]3CC4=C(C=CO4)[C@H](C)[C@@H]3CC[C@@H]12)C(O)=O)OC(C)=O

InChI Identifier

InChI=1S/C23H30O7/c1-12-14-5-6-18-22(3,21(27)28-4)19(30-13(2)24)7-9-23(18,20(25)26)16(14)11-17-15(12)8-10-29-17/h8,10,12,14,16,18-19H,5-7,9,11H2,1-4H3,(H,25,26)/t12-,14+,16+,18+,19+,22-,23+/m1/s1

InChI Key

RZUPNWIKIOESCU-GILHYWDNSA-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 steroid acids. Steroid acids are compounds containing a carboxyl group attached to a steroid backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid acids

Direct Parent

Steroid acids

Alternative Parents

Substituents

Diterpenoid
Steroid acid
Naphthofuran
Benzofuran
Tricarboxylic acid or derivatives
Heteroaromatic compound
Furan
Methyl ester
Carboxylic acid ester
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.24	ChemAxon
pKa (Strongest Acidic)	4.6	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	103.04 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	106 m³·mol⁻¹	ChemAxon
Polarizability	44.28 Å³	ChemAxon
Number of Rings	4	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

76795759

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102036351

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid (NP0251111)

MOL for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)

3D MOL for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)

3D SDF for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)

3D-SDF for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)

PDB for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)

3D PDB for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)

SMILES for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)

INCHI for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)

Structure for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)

3D Structure for NP0251111 ((3s,4r,4ar,6as,7r,11as,11bs)-3-(acetyloxy)-4-(methoxycarbonyl)-4,7-dimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-11b-carboxylic acid)