NP-MRD: Showing NP-Card for (1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde (NP0263933)

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Record Information

Version

2.0

Created at

2022-09-08 07:16:58 UTC

Updated at

2022-09-08 07:16:58 UTC

NP-MRD ID

NP0263933

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde

Description

(1S,2R,7R,10R,11R,14S,15R,17R)-14-[(2E,4S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-17-hydroxy-6,6,10,11-tetramethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-2-carbaldehyde belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde is found in Varronia multispicata. Based on a literature review very few articles have been published on (1S,2R,7R,10R,11R,14S,15R,17R)-14-[(2E,4S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-17-hydroxy-6,6,10,11-tetramethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-2-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082209162D          

 35 39  0  0  1  0            999 V2000
    0.7294   -1.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4185   -1.9676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3987   -2.0804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9051   -1.4291    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7223   -1.5419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5942   -0.6649    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7071    0.1523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0571   -0.1585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6618    0.4026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7913   -0.5349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 20 18  1  6  0  0  0
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 33 34  1  0  0  0  0
 20 34  1  0  0  0  0
 14 34  1  0  0  0  0
 34 35  1  6  0  0  0
M  END

     RDKit          3D

 81 85  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309082209162D          

 35 39  0  0  1  0            999 V2000
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    4.4373   -1.6211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7176   -2.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5297   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8100   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6221   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2782   -3.9489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9917   -4.3631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9942   -4.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4661   -3.8037    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9343   -4.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1221   -4.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5309   -4.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  4  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 11  2  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 20 18  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  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
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 21 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 20 34  1  0  0  0  0
 14 34  1  0  0  0  0
 34 35  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0263933

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(=C/[C@H](O)[C@H]1OC1(C)C)[C@H]1CC[C@]2(C)[C@@H]1C[C@@H](O)[C@H]1[C@@]2(C)CC[C@H]2C(C)(C)C(=O)CC[C@]12C=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H46O5/c1-17(14-21(33)25-27(4,5)35-25)18-8-11-28(6)19(18)15-20(32)24-29(28,7)12-9-22-26(2,3)23(34)10-13-30(22,24)16-31/h14,16,18-22,24-25,32-33H,8-13,15H2,1-7H3/b17-14+/t18-,19-,20-,21+,22+,24+,25-,28-,29-,30-/m1/s1

> <INCHI_KEY>
VELIIAYHTAVWLG-LJOLEPTGSA-N

> <FORMULA>
C30H46O5

> <MOLECULAR_WEIGHT>
486.693

> <EXACT_MASS>
486.334524581

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
56.0896029916139

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,7R,10R,11R,14S,15R,17R)-14-[(2E,4S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-17-hydroxy-6,6,10,11-tetramethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

> <JCHEM_LOGP>
4.140438215666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.917048166681262

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.699185385697302

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8477672127639284

> <JCHEM_POLAR_SURFACE_AREA>
87.13

> <JCHEM_REFRACTIVITY>
136.41830000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,7R,10R,11R,14S,15R,17R)-14-[(2E,4S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-17-hydroxy-6,6,10,11-tetramethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       1.362  -2.246   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.744  -3.883   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.690  -2.668   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -3.215  -2.878   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.109  -1.241   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.320   0.284   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.107  -0.296   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.235   0.752   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.477  -0.998   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.158  -7.782   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.767  -2.755   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.283  -3.026   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.184  -8.144   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.322  -8.817   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.724  -7.984   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6    8                                                       
CONECT    8    7    6    9   10                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    2   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   34                                             
CONECT   15   14                                                            
CONECT   16   14   11   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   34                                                  
CONECT   21   20   22   24   31                                             
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28   21   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   20   14   35                                             
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₆O₅

Average Mass

486.6930 Da

Monoisotopic Mass

486.33452 Da

IUPAC Name

(1S,2R,7R,10R,11R,14S,15R,17R)-14-[(2E,4S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-17-hydroxy-6,6,10,11-tetramethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

Traditional Name

(1S,2R,7R,10R,11R,14S,15R,17R)-14-[(2E,4S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-17-hydroxy-6,6,10,11-tetramethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

CAS Registry Number

Not Available

SMILES

C\C(=C/[C@H](O)[C@H]1OC1(C)C)[C@H]1CC[C@]2(C)[C@@H]1C[C@@H](O)[C@H]1[C@@]2(C)CC[C@H]2C(C)(C)C(=O)CC[C@]12C=O

InChI Identifier

InChI=1S/C30H46O5/c1-17(14-21(33)25-27(4,5)35-25)18-8-11-28(6)19(18)15-20(32)24-29(28,7)12-9-22-26(2,3)23(34)10-13-30(22,24)16-31/h14,16,18-22,24-25,32-33H,8-13,15H2,1-7H3/b17-14+/t18-,19-,20-,21+,22+,24+,25-,28-,29-,30-/m1/s1

InChI Key

VELIIAYHTAVWLG-LJOLEPTGSA-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
Varronia multispicata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
19-oxosteroid
3-oxosteroid
14-alpha-methylsteroid
Hydroxysteroid
Oxosteroid
3-oxo-5-alpha-steroid
11-hydroxysteroid
11-alpha-hydroxysteroid
Steroid
Cyclic alcohol
Ketone
Secondary alcohol
Cyclic ketone
Oxacycle
Ether
Oxirane
Dialkyl ether
Organoheterocyclic compound
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
Aldehyde
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	4.14	ChemAxon
pKa (Strongest Acidic)	13.7	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	87.13 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	136.42 m³·mol⁻¹	ChemAxon
Polarizability	56.09 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

163021256

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde (NP0263933)

MOL for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D MOL for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D SDF for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D-SDF for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

PDB for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D PDB for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

SMILES for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

INCHI for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

Structure for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D Structure for NP0263933 ((1s,3ar,3br,5ar,9ar,9bs,10r,11ar)-1-[(2e,4s)-4-[(2r)-3,3-dimethyloxiran-2-yl]-4-hydroxybut-2-en-2-yl]-10-hydroxy-3a,3b,6,6-tetramethyl-7-oxo-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)