NP-MRD: Showing NP-Card for Withastramonolide F (NP0332986)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2024-05-03 03:54:40 UTC

Updated at

2024-05-03 03:59:43 UTC

NP-MRD ID

NP0332986

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Withastramonolide F

Description

Not Available

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01152306312D          

 51 56  0  0  1  0            999 V2000
   -3.8244   -0.8429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0071   -0.7301    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5008   -1.3814    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3110   -1.5369    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7301   -2.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0473   -2.6369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3959   -2.1305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8641   -1.4998    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838   -2.2757    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1156   -2.9064    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3035   -3.0516    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8353   -3.6824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5550   -4.4583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0868   -5.0890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5086   -3.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0404   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7601   -1.7902    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4798   -1.0143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0520   -1.6450    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2283   -2.4209    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3323   -0.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1444   -0.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6762   -1.3546    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0361   -0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8526   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3844   -2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1041   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2920   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117   -0.3836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6962    0.0341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5135   -0.0787    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2026    0.6855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8917    1.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0745    1.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7636    2.3267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9463    2.4395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6354    3.2037    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1418    3.8550    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9590    3.7422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1818    3.3165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4927    4.0807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3099    4.1936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6208    4.9578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0137    4.7321    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2972    5.4962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8309    4.6192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3373    5.2705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5681    0.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7509    1.0240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8790    0.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3981    2.1010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  3  2  1  6  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  0  0  0  0
  7  8  1  1  0  0  0
  9  7  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  2  0  0  0  0
 17 16  1  0  0  0  0
 17 18  1  6  0  0  0
 19 17  1  0  0  0  0
  9 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
 23 22  1  0  0  0  0
  7 23  1  0  0  0  0
 23  3  1  0  0  0  0
 23 24  1  6  0  0  0
 16 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  2  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 37 36  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  6  0  0  0
 37 40  1  0  0  0  0
 41 40  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
 44 45  1  6  0  0  0
 44 46  1  0  0  0  0
 38 46  1  0  0  0  0
 46 47  1  0  0  0  0
 34 48  2  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
 30 50  1  0  0  0  0
 33 51  2  0  0  0  0
M  END


  Mrv2104 01152306312D          

 51 56  0  0  1  0            999 V2000
   -3.8244   -0.8429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0071   -0.7301    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5008   -1.3814    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3110   -1.5369    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7301   -2.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0473   -2.6369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3959   -2.1305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8641   -1.4998    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838   -2.2757    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1156   -2.9064    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3035   -3.0516    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8353   -3.6824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5550   -4.4583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0868   -5.0890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5086   -3.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0404   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7601   -1.7902    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4798   -1.0143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0520   -1.6450    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2283   -2.4209    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3323   -0.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1444   -0.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6762   -1.3546    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0361   -0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8526   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3844   -2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1041   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2920   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117   -0.3836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6962    0.0341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5135   -0.0787    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2026    0.6855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8917    1.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0745    1.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7636    2.3267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9463    2.4395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6354    3.2037    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1418    3.8550    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9590    3.7422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1818    3.3165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4927    4.0807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3099    4.1936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6208    4.9578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0137    4.7321    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2972    5.4962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8309    4.6192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3373    5.2705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5681    0.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7509    1.0240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8790    0.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3981    2.1010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  3  2  1  6  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  0  0  0  0
  7  8  1  1  0  0  0
  9  7  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  2  0  0  0  0
 17 16  1  0  0  0  0
 17 18  1  6  0  0  0
 19 17  1  0  0  0  0
  9 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
 23 22  1  0  0  0  0
  7 23  1  0  0  0  0
 23  3  1  0  0  0  0
 23 24  1  6  0  0  0
 16 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  2  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 37 36  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  6  0  0  0
 37 40  1  0  0  0  0
 41 40  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
 44 45  1  6  0  0  0
 44 46  1  0  0  0  0
 38 46  1  0  0  0  0
 46 47  1  0  0  0  0
 34 48  2  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
 30 50  1  0  0  0  0
 33 51  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0332986

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](OCC)C=C4C=CCC(=O)[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)[C@@]1([H])CC(C)=C(CO[C@@H]2O[C@H](CO)[C@@H](O)C(O)[C@H]2O)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C36H52O10/c1-6-43-26-15-20-8-7-9-28(38)36(20,5)24-12-13-35(4)22(10-11-23(35)29(24)26)19(3)25-14-18(2)21(33(42)45-25)17-44-34-32(41)31(40)30(39)27(16-37)46-34/h7-8,15,19,22-27,29-32,34,37,39-41H,6,9-14,16-17H2,1-5H3/t19-,22+,23-,24-,25+,26+,27+,29-,30+,31?,32+,34+,35+,36-/m0/s1

> <INCHI_KEY>
BJLILHIABIJQMX-ICQVLRJQSA-N

> <FORMULA>
C36H52O10

> <MOLECULAR_WEIGHT>
644.802

> <EXACT_MASS>
644.356047874

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
72.25836231135153

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6R)-6-[(1S)-1-[(1R,3aS,3bS,4S,9aR,9bS,11aR)-4-ethoxy-9a,11a-dimethyl-9-oxo-1H,2H,3H,3aH,3bH,4H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl]ethyl]-4-methyl-3-({[(2R,3R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-5,6-dihydro-2H-pyran-2-one

> <JCHEM_LOGP>
2.884386908999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.19892634068854

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210361822939698

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083553717509

> <JCHEM_POLAR_SURFACE_AREA>
151.98000000000002

> <JCHEM_REFRACTIVITY>
170.83260000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(6R)-6-[(1S)-1-[(1R,3aS,3bS,4S,9aR,9bS,11aR)-4-ethoxy-9a,11a-dimethyl-9-oxo-1H,2H,3H,3aH,3bH,4H,8H,9bH,10H,11H-cyclopenta[a]phenanthren-1-yl]ethyl]-4-methyl-3-({[(2R,3R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-5,6-dihydropyran-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-JAN-23         0                                  
HETATM    1  C   UNK     0      -7.139  -1.573   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.613  -1.363   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.668  -2.579   0.000  0.00  0.00           C+0
HETATM    4  H   UNK     0      -6.181  -2.869   0.000  0.00  0.00           H+0
HETATM    5  C   UNK     0      -5.096  -4.058   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.822  -4.922   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.606  -3.977   0.000  0.00  0.00           C+0
HETATM    8  H   UNK     0      -1.613  -2.800   0.000  0.00  0.00           H+0
HETATM    9  C   UNK     0      -1.090  -4.248   0.000  0.00  0.00           C+0
HETATM   10  H   UNK     0      -2.082  -5.425   0.000  0.00  0.00           H+0
HETATM   11  C   UNK     0      -0.567  -5.696   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.559  -6.874   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.036  -8.322   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.029  -9.499   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.949  -5.967   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.942  -4.790   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.419  -3.342   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.896  -1.893   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.097  -3.071   0.000  0.00  0.00           C+0
HETATM   20  H   UNK     0       0.426  -4.519   0.000  0.00  0.00           H+0
HETATM   21  C   UNK     0      -0.620  -1.622   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.136  -1.351   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.129  -2.529   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.801  -1.143   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.458  -5.061   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.451  -3.884   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.928  -2.436   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.412  -2.164   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.888  -0.716   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -5.033   0.064   0.000  0.00  0.00           C+0
HETATM   31  H   UNK     0      -6.559  -0.147   0.000  0.00  0.00           H+0
HETATM   32  O   UNK     0      -5.978   1.280   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -5.398   2.706   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -3.872   2.917   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -3.292   4.343   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -1.766   4.554   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -1.186   5.980   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -2.131   7.196   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -3.657   6.985   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       0.339   6.191   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       0.920   7.617   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.445   7.828   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       3.026   9.254   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -0.025   8.833   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       0.555  10.260   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -1.551   8.623   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -2.496   9.838   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -2.927   1.701   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -1.402   1.911   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -3.507   0.274   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -6.343   3.922   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4    5   23                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   23                                             
CONECT    8    7                                                            
CONECT    9    7   10   11   19                                             
CONECT   10    9                                                            
CONECT   11    9   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   11   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18   19   28                                             
CONECT   18   17                                                            
CONECT   19   17    9   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    7    3   24                                             
CONECT   24   23                                                            
CONECT   25   16   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   17   29                                                  
CONECT   29   28                                                            
CONECT   30    2   31   32   50                                             
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   51                                                  
CONECT   34   33   35   48                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   40                                                  
CONECT   38   37   39   46                                                  
CONECT   39   38                                                            
CONECT   40   37   41                                                       
CONECT   41   40   42   44                                                  
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   41   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   38   47                                                  
CONECT   47   46                                                            
CONECT   48   34   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   30                                                       
CONECT   51   33                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  112    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₅₂O₁₀

Average Mass

644.8020 Da

Monoisotopic Mass

644.35605 Da

IUPAC Name

(6R)-6-[(1S)-1-[(1R,3aS,3bS,4S,9aR,9bS,11aR)-4-ethoxy-9a,11a-dimethyl-9-oxo-1H,2H,3H,3aH,3bH,4H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl]ethyl]-4-methyl-3-({[(2R,3R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-5,6-dihydro-2H-pyran-2-one

Traditional Name

(6R)-6-[(1S)-1-[(1R,3aS,3bS,4S,9aR,9bS,11aR)-4-ethoxy-9a,11a-dimethyl-9-oxo-1H,2H,3H,3aH,3bH,4H,8H,9bH,10H,11H-cyclopenta[a]phenanthren-1-yl]ethyl]-4-methyl-3-({[(2R,3R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-5,6-dihydropyran-2-one

CAS Registry Number

Not Available

SMILES

[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](OCC)C=C4C=CCC(=O)[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)[C@@]1([H])CC(C)=C(CO[C@@H]2O[C@H](CO)[C@@H](O)C(O)[C@H]2O)C(=O)O1

InChI Identifier

InChI=1S/C36H52O10/c1-6-43-26-15-20-8-7-9-28(38)36(20,5)24-12-13-35(4)22(10-11-23(35)29(24)26)19(3)25-14-18(2)21(33(42)45-25)17-44-34-32(41)31(40)30(39)27(16-37)46-34/h7-8,15,19,22-27,29-32,34,37,39-41H,6,9-14,16-17H2,1-5H3/t19-,22+,23-,24-,25+,26+,27+,29-,30+,31?,32+,34+,35+,36-/m0/s1

InChI Key

BJLILHIABIJQMX-ICQVLRJQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View

Predicted Spectra

Not Available

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 600, CD₃OD, simulated)	570075670@qq.com	黑龙江中医药大学	Pan juan	2024-05-03	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
stramonium		Not Available

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2.88	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	151.98 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	170.83 m³·mol⁻¹	ChemAxon
Polarizability	72.26 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

Not Available

References

General References

Pan J, Liu Y, Li XY, Wang SY, Wu JT, Li MM, Guan W, Mohammed Algradi A, Kuang HX, Yang BY: Cytotoxic withanolides from the leaves of Datura stramonium L. Chem Biodivers. 2024 Feb;21(2):e202301655. doi: 10.1002/cbdv.202301655. Epub 2024 Jan 12. [PubMed:38084071 ]

Showing NP-Card for Withastramonolide F (NP0332986)

MOL for NP0332986 (Withastramonolide F)

3D MOL for NP0332986 (Withastramonolide F)

3D SDF for NP0332986 (Withastramonolide F)

3D-SDF for NP0332986 (Withastramonolide F)

PDB for NP0332986 (Withastramonolide F)

3D PDB for NP0332986 (Withastramonolide F)

SMILES for NP0332986 (Withastramonolide F)

INCHI for NP0332986 (Withastramonolide F)

Structure for NP0332986 (Withastramonolide F)

3D Structure for NP0332986 (Withastramonolide F)