NP-MRD: Showing NP-Card for (1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde (NP0302424)

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Record Information

Version

2.0

Created at

2022-09-10 15:57:41 UTC

Updated at

2022-09-10 15:57:41 UTC

NP-MRD ID

NP0302424

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde

Description

(1S,2S,4R,10R,11S,14R,15R)-4,5,11-trihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-7-ene-2-carbaldehyde belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton. (1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde is found in Gomphocarpus sinaicus. Based on a literature review very few articles have been published on (1S,2S,4R,10R,11S,14R,15R)-4,5,11-trihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-7-ene-2-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102217572D          

 29 33  0  0  1  0            999 V2000
    3.5330   -3.2587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171   -2.2259    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9853   -1.5952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2655   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0777   -0.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4216   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7655   -1.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6731   -2.5662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2049   -3.1969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8610   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3292   -2.0807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0489   -2.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5807   -3.4873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1731   -1.7404    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3708   -0.9394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -1.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5619   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7912   -3.9333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1084   -4.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0816   -5.2209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4570   -3.8899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7373   -3.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
  6 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
M  END

     RDKit          3D

 59 63  0  0  0  0  0  0  0  0999 V2000
    2.6639   -1.3211   -1.1945 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9913   -0.3620   -0.2623 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0601   -1.0884    0.6907 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0391   -0.1695    1.3120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580    0.4767    0.2755 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2203    0.2459   -1.0691 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0515    0.8560   -2.1831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3884    0.2176   -2.0987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9266   -0.1914   -0.9821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2725   -0.8185   -1.0084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1678    0.0739   -0.1385 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.4206   -0.4791    0.0193 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5215    0.1872    1.2023 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3658    0.9416    2.0226 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1611    0.8504    1.1627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2471   -0.0534    0.3131 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3124   -1.3955    0.9822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1567   -2.3756    0.2621 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2138    0.6277   -1.1391 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6178    0.5628   -2.4730 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5404    1.9945   -0.6419 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9802    1.7887   -0.1431 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9286    0.4597    0.5554 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2588   -0.1778    0.7253 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4192    0.3047    0.3422 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4334   -0.6679    0.7206 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6717   -0.5560    0.5180 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8103   -1.7330    1.3385 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4489   -1.4770    1.3782 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7637   -1.1815   -1.2318 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3751   -2.3875   -0.9687 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3339   -1.2004   -2.2686 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7018   -1.4555    1.5242 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014   -1.9716    0.2354 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5404    0.5803    1.9529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5648   -0.8002    2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9180    1.5757    0.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2731   -0.8687   -1.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0951    1.9612   -2.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5733    0.5355   -3.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9351    0.0954   -3.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2913   -1.8151   -0.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6718   -0.9301   -2.0266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1975    1.0537   -0.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3563   -1.2208    0.6499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4396   -0.8065    1.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5374    1.8408    1.6528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7873    0.8876    2.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2023    1.8688    0.7705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4878   -1.4733    2.0411 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4577    1.4613   -2.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9627    2.3138    0.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5854    2.7468   -1.4369 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6942    1.7717   -0.9725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2254    2.5623    0.6263 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5451    0.6247    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6107    1.2665   -0.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0399   -1.4563    2.4182 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8859   -2.2997    0.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  1
 17 18  2  0
  6 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  1  0
 19  2  1  0
 29 24  1  0
 23  2  1  0
 16  5  1  0
 16  9  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  6 38  1  6
  7 39  1  0
  7 40  1  0
  8 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  6
 12 45  1  0
 13 46  1  1
 14 47  1  0
 15 48  1  0
 15 49  1  0
 17 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  0
 22 55  1  0
 23 56  1  1
 25 57  1  0
 29 58  1  0
 29 59  1  0
M  END


  Mrv1652309102217572D          

 29 33  0  0  1  0            999 V2000
    3.5330   -3.2587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171   -2.2259    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9853   -1.5952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2655   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0777   -0.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4216   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7655   -1.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6731   -2.5662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2049   -3.1969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8610   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3292   -2.0807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0489   -2.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5807   -3.4873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1731   -1.7404    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3708   -0.9394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -1.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5619   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7912   -3.9333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1084   -4.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0816   -5.2209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4570   -3.8899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7373   -3.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
  6 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0302424

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12CC[C@H]3[C@@H](CC=C4CC(O)[C@H](O)C[C@]34C=O)[C@@]1(O)CC[C@@H]2C1=CC(=O)OC1

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O6/c1-21-6-4-16-17(3-2-14-9-18(25)19(26)10-22(14,16)12-24)23(21,28)7-5-15(21)13-8-20(27)29-11-13/h2,8,12,15-19,25-26,28H,3-7,9-11H2,1H3/t15-,16+,17-,18?,19-,21-,22-,23+/m1/s1

> <INCHI_KEY>
FJXWBXGFWCHFFE-LHUTUEIVSA-N

> <FORMULA>
C23H30O6

> <MOLECULAR_WEIGHT>
402.487

> <EXACT_MASS>
402.204238686

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.80143751395269

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,4R,10R,11S,14R,15R)-4,5,11-trihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-2-carbaldehyde

> <JCHEM_LOGP>
0.6199478453333322

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.845023683300372

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.182633655454735

> <JCHEM_PKA_STRONGEST_BASIC>
0.3016534123529262

> <JCHEM_POLAR_SURFACE_AREA>
104.06000000000002

> <JCHEM_REFRACTIVITY>
106.64389999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4R,10R,11S,14R,15R)-4,5,11-trihydroxy-15-methyl-14-(5-oxo-2H-furan-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-2-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       6.595  -6.083   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      16.362  -3.071   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      15.316  -5.967   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      12.284  -6.510   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.159  -1.754   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.782  -5.863   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.210  -7.342   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.936  -8.206   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.886  -9.746   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.720  -7.261   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.243  -5.813   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19   23                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   16                                                  
CONECT    6    5    7   19                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    9    5   17                                             
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19    6    2   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    2   24                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   24                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₀O₆

Average Mass

402.4870 Da

Monoisotopic Mass

402.20424 Da

IUPAC Name

(1S,2S,4R,10R,11S,14R,15R)-4,5,11-trihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-2-carbaldehyde

Traditional Name

(1S,2S,4R,10R,11S,14R,15R)-4,5,11-trihydroxy-15-methyl-14-(5-oxo-2H-furan-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-2-carbaldehyde

CAS Registry Number

Not Available

SMILES

C[C@]12CC[C@H]3[C@@H](CC=C4CC(O)[C@H](O)C[C@]34C=O)[C@@]1(O)CC[C@@H]2C1=CC(=O)OC1

InChI Identifier

InChI=1S/C23H30O6/c1-21-6-4-16-17(3-2-14-9-18(25)19(26)10-22(14,16)12-24)23(21,28)7-5-15(21)13-8-20(27)29-11-13/h2,8,12,15-19,25-26,28H,3-7,9-11H2,1H3/t15-,16+,17-,18?,19-,21-,22-,23+/m1/s1

InChI Key

FJXWBXGFWCHFFE-LHUTUEIVSA-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
Gomphocarpus sinaicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Steroid lactones

Alternative Parents

Substituents

Steroid lactone
19-oxosteroid
Androgen-skeleton
Androstane-skeleton
Oxosteroid
Hydroxysteroid
14-hydroxysteroid
2-hydroxysteroid
3-hydroxysteroid
3-hydroxy-delta-5-steroid
Delta-5-steroid
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Dihydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
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	0.62	ChemAxon
pKa (Strongest Acidic)	7.18	ChemAxon
pKa (Strongest Basic)	0.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	106.64 m³·mol⁻¹	ChemAxon
Polarizability	42.8 Å³	ChemAxon
Number of Rings	5	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

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

162986798

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde (NP0302424)

MOL for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D MOL for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D SDF for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D-SDF for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

PDB for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D PDB for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

SMILES for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

INCHI for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

Structure for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D Structure for NP0302424 ((1r,3as,3br,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde)