NP-MRD: Showing NP-Card for methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate (NP0194412)

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Record Information

Version

2.0

Created at

2022-09-04 12:03:49 UTC

Updated at

2022-09-04 12:03:50 UTC

NP-MRD ID

NP0194412

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate

Description

Cassamide belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate is found in Erythrophleum fordii. methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate was first documented in 2006 (PMID: 16557459). Based on a literature review very few articles have been published on Cassamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042214032D          

 30 32  0  0  1  0            999 V2000
   -7.8710    4.6045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0585    4.4613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5282    5.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8104    5.8685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9979    4.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  0  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
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    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
    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    4.5375    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  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 12 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 30 29  1  1  0  0  0
  5 30  1  0  0  0  0
 10 30  1  0  0  0  0
M  END

     RDKit          3D

 67 69  0  0  0  0  0  0  0  0999 V2000
   -5.3821    2.1295   -2.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5150    1.9812   -0.9782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6245    0.8792   -0.1475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5319    0.0494   -0.4301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7775    0.6183    1.0101 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9067    1.8193    1.9546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3004   -0.5644    1.8124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9376   -1.8772    1.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4913   -2.0137    0.8621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9959   -0.8552   -0.0051 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6583   -0.9713   -1.3344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5153   -0.9226   -0.1133 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0821   -2.1992   -0.5744 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5858   -2.0919   -0.2207 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1000   -0.8424   -0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3386   -0.4380   -0.6136 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2799   -1.1857    0.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8944   -2.2535    0.7278 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6111   -0.7524    0.4254 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4724   -1.5624    1.2627 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1465    0.4529   -0.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071    1.6517    0.7783 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4277    2.8071    0.2142 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2216   -0.0313   -1.6729 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8924    1.1998   -2.2266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0985    0.1998   -1.0749 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3115    1.4343   -0.3095 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5233    2.2824   -0.0906 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6769    1.6477    0.2386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3292    0.4108    0.7548 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7178    1.1810   -2.5122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2673    2.7566   -1.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8245    2.6735   -2.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7610    2.7710    1.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0651    1.7187    2.6740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8681    1.7863    2.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0525   -0.4833    2.8887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4260   -0.4822    1.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1525   -2.6621    1.9854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6257   -2.1389    0.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3546   -2.9861    0.3375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9132   -2.0823    1.8092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9382   -1.5239   -2.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8776   -0.0331   -1.8519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5568   -1.6511   -1.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1053   -0.6552    0.9039 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0482   -2.3284   -1.6632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2824   -3.0598    0.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6336   -2.0507    0.8929 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1320   -2.9551   -0.6201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7036    0.5006   -1.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8691   -2.1094    2.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2219   -0.8857    1.7426 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9821   -2.2919    0.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7000    0.6636   -1.1356 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2641    0.3181   -0.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3997    1.4313    1.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8231    1.8030    0.9196 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8356    3.0794   -0.5270 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0475   -0.6826   -2.5961 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1953    1.6557   -2.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581    0.8269   -2.8460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    1.8858   -1.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8642    0.2393   -1.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5891    2.3606    1.0840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2400    2.1696   -0.5606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8694    0.2387    1.7793 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  6
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 15 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  0
 30  5  1  0
 30 10  1  0
 26 12  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  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
 11 43  1  0
 11 44  1  0
 11 45  1  0
 12 46  1  1
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 16 51  1  0
 20 52  1  0
 20 53  1  0
 20 54  1  0
 21 55  1  0
 21 56  1  0
 22 57  1  0
 22 58  1  0
 23 59  1  0
 24 60  1  6
 25 61  1  0
 25 62  1  0
 25 63  1  0
 26 64  1  6
 29 65  1  0
 29 66  1  0
 30 67  1  1
M  END


  Mrv1652309042214032D          

 30 32  0  0  1  0            999 V2000
   -7.8710    4.6045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0585    4.4613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5282    5.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8104    5.8685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9979    4.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  0  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
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    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
    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    4.5375    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  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 12 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 30 29  1  1  0  0  0
  5 30  1  0  0  0  0
 10 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0194412

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]1(C)CCC[C@]2(C)[C@H]3CC\C(=C/C(=O)N(C)CCO)[C@H](C)[C@@H]3C(=O)C[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C24H37NO5/c1-15-16(13-20(28)25(4)11-12-26)7-8-17-21(15)18(27)14-19-23(17,2)9-6-10-24(19,3)22(29)30-5/h13,15,17,19,21,26H,6-12,14H2,1-5H3/b16-13+/t15-,17-,19+,21-,23+,24-/m0/s1

> <INCHI_KEY>
HXLYBWISMCTBNI-YGFGEUBNSA-N

> <FORMULA>
C24H37NO5

> <MOLECULAR_WEIGHT>
419.562

> <EXACT_MASS>
419.267173295

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
47.17459611596507

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,4aR,4bS,7E,8R,8aS,10aR)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-tetradecahydrophenanthrene-1-carboxylate

> <JCHEM_LOGP>
2.5705989413333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.073231502611087

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.574125258075966

> <JCHEM_PKA_STRONGEST_BASIC>
-0.018297531677682888

> <JCHEM_POLAR_SURFACE_AREA>
83.91

> <JCHEM_REFRACTIVITY>
115.35059999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,4aR,4bS,7E,8R,8aS,10aR)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0     -14.693   8.595   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -13.176   8.328   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0     -12.186   9.507   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0     -12.713  10.955   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0     -10.669   9.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -11.196   7.793   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.669  10.780   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -9.336  11.550   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.002  10.780   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -8.002   9.240   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.668  10.010   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.668   8.470   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.335   9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001   8.470   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.334   8.470   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0      -0.000   6.160   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.001   6.930   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -5.335   6.160   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.668   6.930   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -8.002   6.160   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -8.002   4.620   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -9.336   6.930   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -9.336   8.470   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                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   30                                             
CONECT   11   10                                                            
CONECT   12   10   13   26                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   15   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   12   27                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29    5   10                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₇NO₅

Average Mass

419.5620 Da

Monoisotopic Mass

419.26717 Da

IUPAC Name

methyl (1S,4aR,4bS,7E,8R,8aS,10aR)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-tetradecahydrophenanthrene-1-carboxylate

Traditional Name

methyl (1S,4aR,4bS,7E,8R,8aS,10aR)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@]1(C)CCC[C@]2(C)[C@H]3CC\C(=C/C(=O)N(C)CCO)[C@H](C)[C@@H]3C(=O)C[C@@H]12

InChI Identifier

InChI=1S/C24H37NO5/c1-15-16(13-20(28)25(4)11-12-26)7-8-17-21(15)18(27)14-19-23(17,2)9-6-10-24(19,3)22(29)30-5/h13,15,17,19,21,26H,6-12,14H2,1-5H3/b16-13+/t15-,17-,19+,21-,23+,24-/m0/s1

InChI Key

HXLYBWISMCTBNI-YGFGEUBNSA-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
Erythrophleum fordii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Cassane diterpenoid
Diterpenoid
Hydrophenanthrene
Phenanthrene
Methyl ester
Tertiary carboxylic acid amide
Carboxamide group
Carboxylic acid ester
Ketone
Alkanolamine
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Primary alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Organooxygen compound
Alcohol
Organonitrogen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.57	ChemAxon
pKa (Strongest Acidic)	15.57	ChemAxon
pKa (Strongest Basic)	-0.018	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	83.91 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	115.35 m³·mol⁻¹	ChemAxon
Polarizability	47.17 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9822163

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11647424

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Qu J, Hu YC, Yu SS, Chen XG, Li Y: New cassaine diterpenoid amides with cytotoxic activities from the bark of Erythrophleum fordii. Planta Med. 2006 Apr;72(5):442-9. doi: 10.1055/s-2005-916264. [PubMed:16557459 ]
LOTUS database [Link]

Showing NP-Card for methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate (NP0194412)

MOL for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)

3D MOL for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)

3D SDF for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)

3D-SDF for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)

PDB for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)

3D PDB for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)

SMILES for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)

INCHI for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)

Structure for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)

3D Structure for NP0194412 (methyl (1s,4ar,4bs,7e,8r,8as,10ar)-7-{[(2-hydroxyethyl)(methyl)carbamoyl]methylidene}-1,4a,8-trimethyl-9-oxo-decahydrophenanthrene-1-carboxylate)