NP-MRD: Showing NP-Card for (1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol (NP0276804)

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Record Information

Version

2.0

Created at

2022-09-09 01:06:19 UTC

Updated at

2022-09-09 01:06:19 UTC

NP-MRD ID

NP0276804

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol

Description

CHEMBL4172688 belongs to the class of organic compounds known as indolizidines. These are polycyclic compounds containing an indolizidine, which is a bicyclic heterocycle containing a saturated six-member ring fused to a saturated five-member ring, one of the bridging atoms being nitrogen. Based on a literature review very few articles have been published on CHEMBL4172688.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
    1.5478   -0.1193    1.9491 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6299    0.0259    0.4939 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8556   -0.4503   -0.2112 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8557   -0.9984    0.4395 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0792   -1.4773   -0.2303 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0956   -0.5376   -0.7591 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1958   -1.3310   -1.7166 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6413    0.5654   -0.1706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5848    1.0484    0.4759 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2154    2.0084   -0.5691 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9106    3.0001    0.0855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1112    1.0196   -1.2864 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0862    1.6964   -2.2102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3216    0.1898   -2.0549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7322    0.3672   -0.1165 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4768   -0.8971   -0.3572 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7856   -0.8705    0.3514 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6561   -1.6485    0.8383 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0555   -1.1974    2.1102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1260   -0.0156    2.0326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5774    0.0590    0.7205 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7978    0.5019    2.4290 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5250   -1.1857    2.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5324    0.2614    2.3694 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8921   -0.3293   -1.2780 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7427   -1.0927    1.5301 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4890   -2.4437    0.2018 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1495   -0.8796   -0.7660 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9300    0.5629   -0.7215 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5062   -0.7546   -2.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6666   -2.1891   -2.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8066    0.6294   -1.2622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4328    1.6530    1.3919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4672    2.4040   -1.2519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8550    3.0621   -0.1169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5158    2.2293   -2.9829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8581    2.2797   -1.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6214    0.8606   -2.7472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2078    0.6319   -2.9471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3251    1.1536    0.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5270   -1.3758   -1.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9381   -2.7300    0.8025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8362   -0.9607    2.8757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4782   -2.0484    2.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7817    0.8967    2.1600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4546   -0.0272    2.8755 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  2  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  6
 12 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
  7  5  1  0
 21  9  1  0
 21 15  1  0
 18 16  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  9 33  1  1
 10 34  1  6
 11 35  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 15 40  1  1
 16 41  1  6
 18 42  1  6
 19 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
M  END


  Mrv1652309092203062D          

 21 24  0  0  1  0            999 V2000
   -0.7311   -0.8352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4917   -1.6247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0557   -2.2267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8164   -3.0163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3804   -3.6183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5679   -4.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1699   -3.8577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3117   -1.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8758   -1.2101    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7202   -0.3999    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0267   -0.0495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4427   -0.0016    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9711    0.6753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0666    0.5382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0448   -0.5656    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8668   -0.4956    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6888   -0.4256    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3384   -1.1725    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9880   -1.9194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1660   -1.9894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6944   -1.3125    0.0000 N   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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  7  1  0  0  0  0
  2  8  2  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  1  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 18 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  9 21  1  0  0  0  0
 15 21  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0276804

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(\C=C\C1CC1)=C/[C@H]1[C@H](O)[C@@](C)(O)[C@H]2[C@@H]3O[C@@H]3CCN12

> <INCHI_IDENTIFIER>
InChI=1S/C17H25NO3/c1-10(3-4-11-5-6-11)9-12-16(19)17(2,20)15-14-13(21-14)7-8-18(12)15/h3-4,9,11-16,19-20H,5-8H2,1-2H3/b4-3+,10-9+/t12-,13+,14+,15+,16-,17-/m0/s1

> <INCHI_KEY>
WGALLPIJABPILU-MUUXAGPVSA-N

> <FORMULA>
C17H25NO3

> <MOLECULAR_WEIGHT>
291.391

> <EXACT_MASS>
291.183443669

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
32.78458164114993

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1aS,1bR,2S,3S,4S,7aR)-4-[(1E,3E)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-2-methyl-octahydrooxireno[2,3-g]indolizine-2,3-diol

> <JCHEM_LOGP>
1.103877552333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.437327031928525

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.038841021500168

> <JCHEM_PKA_STRONGEST_BASIC>
8.834325484192599

> <JCHEM_POLAR_SURFACE_AREA>
56.230000000000004

> <JCHEM_REFRACTIVITY>
82.01820000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1aS,1bR,2S,3S,4S,7aR)-4-[(1E,3E)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-2-methyl-hexahydro-1aH-oxireno[2,3-g]indolizine-2,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.365  -1.559   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.918  -3.033   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.971  -4.157   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.524  -5.630   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.577  -6.754   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.927  -8.254   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.051  -7.201   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.582  -3.383   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.635  -2.259   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.344  -0.746   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.050  -0.092   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.693  -0.003   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.813   1.261   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.858   1.005   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.817  -1.056   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.351  -0.925   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.886  -0.795   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.232  -2.189   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.578  -3.583   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.043  -3.714   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       3.163  -2.450   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    7                                                       
CONECT    7    6    5                                                       
CONECT    8    2    9                                                       
CONECT    9    8   10   21                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16   21                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   18                                                       
CONECT   18   17   16   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    9   15                                                  
MASTER        0    0    0    0    0    0    0    0   21    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₅NO₃

Average Mass

291.3910 Da

Monoisotopic Mass

291.18344 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C(\C=C\C1CC1)=C/[C@H]1[C@H](O)[C@@](C)(O)[C@H]2[C@@H]3O[C@@H]3CCN12

InChI Identifier

InChI=1S/C17H25NO3/c1-10(3-4-11-5-6-11)9-12-16(19)17(2,20)15-14-13(21-14)7-8-18(12)15/h3-4,9,11-16,19-20H,5-8H2,1-2H3/b4-3+,10-9+/t12-,13+,14+,15+,16-,17-/m0/s1

InChI Key

WGALLPIJABPILU-MUUXAGPVSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indolizidines. These are polycyclic compounds containing an indolizidine, which is a bicyclic heterocycle containing a saturated six-member ring fused to a saturated five-member ring, one of the bridging atoms being nitrogen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indolizidines

Sub Class

Not Available

Direct Parent

Indolizidines

Alternative Parents

Substituents

Indolizidine
Para-oxazepine
Epoxypiperidine
Piperidine
N-alkylpyrrolidine
Tertiary alcohol
Pyrrolidine
1,2-diol
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
1,2-aminoalcohol
Azacycle
Oxacycle
Dialkyl ether
Oxirane
Ether
Hydrocarbon derivative
Organic oxygen compound
Organopnictogen compound
Organonitrogen compound
Amine
Alcohol
Organic nitrogen compound
Organooxygen compound
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	1.1	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

8170012

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9994431

PDB ID

Not Available

ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol (NP0276804)

MOL for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)

3D MOL for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)

3D SDF for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)

3D-SDF for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)

PDB for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)

3D PDB for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)

SMILES for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)

INCHI for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)

Structure for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)

3D Structure for NP0276804 ((1ar,5s,6s,7s,7ar,7bs)-5-[(1e,3e)-4-cyclopropyl-2-methylbuta-1,3-dien-1-yl]-7-methyl-hexahydro-1ah-oxireno[2,3-g]indolizine-6,7-diol)