NP-MRD: Showing NP-Card for (1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane (NP0314027)

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Record Information

Version

2.0

Created at

2022-09-11 11:55:02 UTC

Updated at

2022-09-11 11:55:02 UTC

NP-MRD ID

NP0314027

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane

Description

(1S,2S,5S,8R,9S,11S,13R,15R,16S,19S)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]Henicosane belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative. (1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane is found in Nuphar lutea. Based on a literature review very few articles have been published on (1S,2S,5S,8R,9S,11S,13R,15R,16S,19S)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]Henicosane.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112213552D          

 35 41  0  0  1  0            999 V2000
    6.3813   -1.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1264   -0.3721    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6784    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4235    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6165    1.1971    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3615    1.9817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8465    2.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3615    3.3166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5769    3.0617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5769    2.2367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5214    0.5840    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3284    0.7556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2 17  1  0  0  0  0
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 33 34  1  0  0  0  0
 19 34  1  0  0  0  0
 13 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END

     RDKit          3D

 77 83  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309112213552D          

 35 41  0  0  1  0            999 V2000
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    1.2243    3.3166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7394    2.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.5840    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3284    0.7556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8804    0.1425    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9667    0.9629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  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
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  2 17  1  0  0  0  0
 17 11  1  1  0  0  0
 15 18  1  1  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 31  2  0  0  0  0
 26 32  1  0  0  0  0
 21 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 19 34  1  0  0  0  0
 13 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0314027

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@H](N2C[C@@]3(C)[C@@H](C[C@H]12)S[C@H]1C[C@H]2[C@H](C)CC[C@H](N2C[C@]31C)C1=COC=C1)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C30H42N2O2S/c1-19-5-7-23(21-9-11-33-15-21)31-17-29(3)27(13-25(19)31)35-28-14-26-20(2)6-8-24(22-10-12-34-16-22)32(26)18-30(28,29)4/h9-12,15-16,19-20,23-28H,5-8,13-14,17-18H2,1-4H3/t19-,20+,23-,24-,25+,26-,27+,28-,29-,30-/m0/s1

> <INCHI_KEY>
IVONUJWNQVEKMR-VMEJAQRISA-N

> <FORMULA>
C30H42N2O2S

> <MOLECULAR_WEIGHT>
494.74

> <EXACT_MASS>
494.296699774

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
56.55275385160921

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,5S,8R,9S,11S,13R,15R,16S,19S)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0^{2,11}.0^{4,9}.0^{15,20}]henicosane

> <JCHEM_LOGP>
5.851750421666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_BASIC>
9.8449579450337

> <JCHEM_POLAR_SURFACE_AREA>
32.760000000000005

> <JCHEM_REFRACTIVITY>
142.6651

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5S,8R,9S,11S,13R,15R,16S,19S)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0^{2,11}.0^{4,9}.0^{15,20}]henicosane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      11.912  -2.159   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.436  -0.695   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.466   0.450   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.990   1.914   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.484   2.235   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.008   3.699   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.913   4.945   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.008   6.191   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.544   5.715   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.544   4.175   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       9.454   1.090   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       7.947   1.410   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.917   0.266   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.290   1.673   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.393  -1.199   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.899  -1.519   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.930  -0.374   0.000  0.00  0.00           C+0
HETATM   18  S   UNK     0       6.147  -2.104   0.000  0.00  0.00           S+0
HETATM   19  C   UNK     0       4.901  -1.199   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.395  -1.519   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.364  -0.374   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.858  -0.695   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.382  -2.159   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.173   0.450   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.303   1.914   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.810   2.235   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.285   3.699   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.750   4.175   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.750   5.715   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.285   6.191   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.380   4.945   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       2.840   1.090   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       4.346   1.410   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.377   0.266   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.538   1.797   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6                                                       
CONECT   11    5   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15   34                                             
CONECT   14   13                                                            
CONECT   15   13   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16    2   11                                                  
CONECT   18   15   19                                                       
CONECT   19   18   20   34                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   32                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   32                                                  
CONECT   27   26   28   31                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   27                                                       
CONECT   32   26   21   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   19   13   35                                             
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₂N₂O₂S

Average Mass

494.7400 Da

Monoisotopic Mass

494.29670 Da

IUPAC Name

(1S,2S,5S,8R,9S,11S,13R,15R,16S,19S)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0^{2,11}.0^{4,9}.0^{15,20}]henicosane

Traditional Name

(1S,2S,5S,8R,9S,11S,13R,15R,16S,19S)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0^{2,11}.0^{4,9}.0^{15,20}]henicosane

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@H](N2C[C@@]3(C)[C@@H](C[C@H]12)S[C@H]1C[C@H]2[C@H](C)CC[C@H](N2C[C@]31C)C1=COC=C1)C1=COC=C1

InChI Identifier

InChI=1S/C30H42N2O2S/c1-19-5-7-23(21-9-11-33-15-21)31-17-29(3)27(13-25(19)31)35-28-14-26-20(2)6-8-24(22-10-12-34-16-22)32(26)18-30(28,29)4/h9-12,15-16,19-20,23-28H,5-8,13-14,17-18H2,1-4H3/t19-,20+,23-,24-,25+,26-,27+,28-,29-,30-/m0/s1

InChI Key

IVONUJWNQVEKMR-VMEJAQRISA-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
Nuphar lutea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizidines

Sub Class

Not Available

Direct Parent

Quinolizidines

Alternative Parents

Substituents

Quinolizidine
Aralkylamine
Piperidine
Furan
Thiolane
Heteroaromatic compound
Tertiary aliphatic amine
Tertiary amine
Azacycle
Dialkylthioether
Thioether
Oxacycle
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Amine
Hydrocarbon derivative
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	5.85	ChemAxon
pKa (Strongest Basic)	9.84	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	32.76 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	142.67 m³·mol⁻¹	ChemAxon
Polarizability	56.55 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

162940529

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane (NP0314027)

MOL for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)

3D MOL for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)

3D SDF for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)

3D-SDF for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)

PDB for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)

3D PDB for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)

SMILES for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)

INCHI for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)

Structure for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)

3D Structure for NP0314027 ((1s,2s,5s,8r,9s,11s,13r,15r,16s,19s)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosane)