NP-MRD: Showing NP-Card for methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate (NP0323561)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 03:03:53 UTC

Updated at

2022-09-12 03:03:54 UTC

NP-MRD ID

NP0323561

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate

Description

CHEMBL4169222 belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate is found in Pterodon pubescens. Based on a literature review very few articles have been published on CHEMBL4169222.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122205032D          

 29 32  0  0  1  0            999 V2000
    3.4599   -2.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1796   -2.2057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7114   -1.5750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5235   -1.7202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0872   -1.2846    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3675   -2.0605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8357   -2.6912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1160   -3.4671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0235   -2.5460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -1.1393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7433   -1.7701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1807   -1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6302   -0.3595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0584    0.8980    0.0000 C   0  0  0  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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  2  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 13 12  1  6  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  6  0  0  0
 21 19  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 12 28  1  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END

     RDKit          3D

 61 64  0  0  0  0  0  0  0  0999 V2000
    5.3274    2.1806    0.1621 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3406    1.3893    0.8199 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1853    1.0268    0.1553 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0317    1.4092   -1.0288 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1176    0.2069    0.7751 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7046   -1.0795    1.1566 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7661   -1.3530    2.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9337   -2.7197    2.0400 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0226   -3.2271    1.2467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2918   -2.3037    0.7173 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1511   -2.3687   -0.2301 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2634   -1.1989    0.0776 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9605    0.0777   -0.1765 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0521    1.2693    0.0844 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6956    2.4875   -0.1230 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9596    3.4342    0.8442 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6516    4.7173    0.5581 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5852    3.1726    2.0180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2678    1.1504   -0.6496 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0488    2.2288   -0.2467 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8850   -0.1366   -0.1989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3282   -0.2892   -0.4730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7101   -0.6533   -1.8649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1505    0.9148   -0.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7958   -1.4310    0.4284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1152   -2.6917    0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6659   -2.6246   -0.2078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0868   -1.3120   -0.6511 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7647   -1.3025   -2.1246 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0008    2.3965   -0.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2779    1.6292    0.1132 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4243    3.1599    0.6745 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189    0.7340    1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3698   -0.6677    2.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6495   -3.3022    2.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6454   -3.3481   -0.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6083   -2.3206   -1.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0079   -1.2534    1.1566 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3491    0.2034   -1.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2057    1.2111    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7188    4.5526    0.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1684    5.1973   -0.3259 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5167    5.4122    1.4032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0816    1.2499   -1.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7998    2.5993    0.6192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7734   -0.1178    0.9313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3375   -1.6106   -2.2317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8383   -0.7599   -1.8603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5465    0.1947   -2.5930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8741    1.3312    0.9037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2054    0.5289    0.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2263    1.6688   -0.8835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4824   -1.1396    1.4606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8760   -1.5523    0.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3618   -3.4494    0.8076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6970   -3.0915   -0.8835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1564   -3.0388    0.7134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3884   -3.3697   -1.0115 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3308   -1.1735   -2.3351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9959   -2.3295   -2.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2616   -0.5184   -2.6987 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
  3  5  1  0
  5 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 14 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  6
 28 12  1  0
 12 11  1  0
 11 10  1  0
 10  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  6  5  1  0
 12 13  1  0
  9 10  1  0
 28 21  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  1
 13 39  1  6
 14 40  1  1
 17 41  1  0
 17 42  1  0
 17 43  1  0
 19 44  1  6
 20 45  1  0
 21 46  1  1
 23 47  1  0
 23 48  1  0
 23 49  1  0
 24 50  1  0
 24 51  1  0
 24 52  1  0
 25 53  1  0
 25 54  1  0
 26 55  1  0
 26 56  1  0
 27 57  1  0
 27 58  1  0
 29 59  1  0
 29 60  1  0
 29 61  1  0
 12 38  1  1
 11 36  1  0
 11 37  1  0
  7 34  1  0
  8 35  1  0
M  END


  Mrv1652309122205032D          

 29 32  0  0  1  0            999 V2000
    3.4599   -2.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1796   -2.2057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7114   -1.5750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5235   -1.7202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0872   -1.2846    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3675   -2.0605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8357   -2.6912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1160   -3.4671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0235   -2.5460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -1.1393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7433   -1.7701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1807   -1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6302   -0.3595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0584    0.8980    0.0000 C   0  0  0  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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  2  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 13 12  1  6  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  6  0  0  0
 21 19  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 12 28  1  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0323561

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@H]1[C@@H]2[C@@H](OC(C)=O)[C@H](O)[C@H]3C(C)(C)CCC[C@]3(C)[C@H]2CC2=C1C=CO2

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O6/c1-12(24)29-19-17-14(11-15-13(7-10-28-15)16(17)21(26)27-5)23(4)9-6-8-22(2,3)20(23)18(19)25/h7,10,14,16-20,25H,6,8-9,11H2,1-5H3/t14-,16+,17+,18-,19+,20-,23+/m0/s1

> <INCHI_KEY>
IEJMZROVWPJSHD-BJXFMLEZSA-N

> <FORMULA>
C23H32O6

> <MOLECULAR_WEIGHT>
404.503

> <EXACT_MASS>
404.21988875

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
44.157149567703584

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,2R,7S,8R,9R,10R,11S)-9-(acetyloxy)-8-hydroxy-2,6,6-trimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-11-carboxylate

> <JCHEM_LOGP>
2.719901087999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.30985394045795

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.886422804340246

> <JCHEM_PKA_STRONGEST_BASIC>
-2.823702791583777

> <JCHEM_POLAR_SURFACE_AREA>
85.97000000000001

> <JCHEM_REFRACTIVITY>
105.61540000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,2R,7S,8R,9R,10R,11S)-9-(acetyloxy)-8-hydroxy-2,6,6-trimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-11-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       6.458  -5.566   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.935  -4.117   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.928  -2.940   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.444  -3.211   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.405  -1.492   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.398  -0.314   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.937  -0.264   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.365   1.215   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.090   2.079   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.874   1.134   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.358   1.405   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.366   0.228   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.889  -1.221   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.896  -2.398   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.419  -3.846   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.427  -5.024   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.950  -6.472   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.911  -4.752   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.380  -2.127   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.387  -3.304   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.857  -0.678   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.341  -0.407   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.337  -1.947   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.176  -0.671   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.182   1.041   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.810   2.218   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.326   1.947   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.850   0.499   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.842   1.676   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   13                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   28                                                  
CONECT   13   12    5   14                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   28                                                  
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   12   21   29                                             
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₆

Average Mass

404.5030 Da

Monoisotopic Mass

404.21989 Da

IUPAC Name

methyl (1S,2R,7S,8R,9R,10R,11S)-9-(acetyloxy)-8-hydroxy-2,6,6-trimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-11-carboxylate

Traditional Name

methyl (1S,2R,7S,8R,9R,10R,11S)-9-(acetyloxy)-8-hydroxy-2,6,6-trimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-11-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@H]1[C@@H]2[C@@H](OC(C)=O)[C@H](O)[C@H]3C(C)(C)CCC[C@]3(C)[C@H]2CC2=C1C=CO2

InChI Identifier

InChI=1S/C23H32O6/c1-12(24)29-19-17-14(11-15-13(7-10-28-15)16(17)21(26)27-5)23(4)9-6-8-22(2,3)20(23)18(19)25/h7,10,14,16-20,25H,6,8-9,11H2,1-5H3/t14-,16+,17+,18-,19+,20-,23+/m0/s1

InChI Key

IEJMZROVWPJSHD-BJXFMLEZSA-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
Pterodon pubescens	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

Diterpenoid
Naphthofuran
Benzofuran
Dicarboxylic acid or derivatives
Heteroaromatic compound
Methyl ester
Furan
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	2.72	ChemAxon
pKa (Strongest Acidic)	13.89	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	85.97 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	105.62 m³·mol⁻¹	ChemAxon
Polarizability	44.16 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

90633296

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

145953917

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate (NP0323561)

MOL for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)

3D MOL for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)

3D SDF for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)

3D-SDF for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)

PDB for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)

3D PDB for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)

SMILES for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)

INCHI for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)

Structure for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)

3D Structure for NP0323561 (methyl (4as,5r,6r,6ar,7s,11as,11br)-6-(acetyloxy)-5-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylate)