NP-MRD: Showing NP-Card for (4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol (NP0201937)

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Record Information

Version

2.0

Created at

2022-09-04 21:03:44 UTC

Updated at

2022-09-04 21:03:44 UTC

NP-MRD ID

NP0201937

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol

Description

(4S,7R,8S,11S,15S,18S)-18-benzyl-7,11-dimethyl-4-(propan-2-yl)-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]Tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. (4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol is found in Lissoclinum bistratum. Based on a literature review very few articles have been published on (4S,7R,8S,11S,15S,18S)-18-benzyl-7,11-dimethyl-4-(propan-2-yl)-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]Tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042223032D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309042223032D          

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    1.9886    5.8982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7132    4.6666    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0021    4.2482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2843    4.6548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0089    3.4232    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7267    3.0166    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7335    2.1916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8802    2.0946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4619    2.8056    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6407    2.8852    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
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  4  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  8 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  4  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  0  0  0  0
 27 28  2  0  0  0  0
 24 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  4  0  0  0
 32 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  2  0  0  0  0
  4 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 34 38  1  0  0  0  0
 38 39  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0201937

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1N=C(O)C2=CSC(=N2)[C@H](CC2=CC=CC=C2)N=C(O)[C@H]2CSC(=N2)[C@H](C)N=C(O)[C@H]2N=C1O[C@@H]2C

> <INCHI_IDENTIFIER>
InChI=1S/C27H32N6O4S2/c1-13(2)20-25-33-21(15(4)37-25)24(36)28-14(3)26-30-18(11-38-26)22(34)29-17(10-16-8-6-5-7-9-16)27-31-19(12-39-27)23(35)32-20/h5-9,12-15,17-18,20-21H,10-11H2,1-4H3,(H,28,36)(H,29,34)(H,32,35)/t14-,15+,17-,18+,20-,21-/m0/s1

> <INCHI_KEY>
BRLJUCBNCZSZRH-AILWYZJWSA-N

> <FORMULA>
C27H32N6O4S2

> <MOLECULAR_WEIGHT>
568.71

> <EXACT_MASS>
568.192645882

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
58.96384644273368

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,7R,8S,11S,15S,18S)-18-benzyl-7,11-dimethyl-4-(propan-2-yl)-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1^{5,8}.1^{12,15}]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol

> <JCHEM_LOGP>
-0.1970467447042377

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
-8.318301849782923

> <JCHEM_PKA_STRONGEST_ACIDIC>
-9.129458492947776

> <JCHEM_PKA_STRONGEST_BASIC>
15.089857836501963

> <JCHEM_POLAR_SURFACE_AREA>
144.60999999999999

> <JCHEM_REFRACTIVITY>
149.3737

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4S,7R,8S,11S,15S,18S)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1^{5,8}.1^{12,15}]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       5.128   1.011   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.455   1.792   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.795   1.033   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.442   3.332   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       7.770   4.113   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       9.110   3.354   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.122   1.814   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.437   4.135   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.946   3.827   0.000  0.00  0.00           C+0
HETATM   10  S   UNK     0      12.705   5.167   0.000  0.00  0.00           S+0
HETATM   11  C   UNK     0      11.752   6.456   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      10.424   5.675   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      11.739   7.996   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.066   8.777   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.406   8.018   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.734   8.798   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.074   8.039   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      17.086   6.499   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      15.759   5.719   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.419   6.478   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      10.399   8.755   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      10.386  10.295   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.714  11.076   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.047  11.054   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.559  12.514   0.000  0.00  0.00           C+0
HETATM   26  S   UNK     0       7.019  12.502   0.000  0.00  0.00           S+0
HETATM   27  C   UNK     0       6.379  11.032   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       7.719  10.273   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       5.052  10.251   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.712  11.010   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       5.065   8.711   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0       3.737   7.930   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.397   8.689   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.750   6.390   0.000  0.00  0.00           C+0
HETATM   35  N   UNK     0       5.090   5.631   0.000  0.00  0.00           N+0
HETATM   36  C   UNK     0       5.102   4.091   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       3.510   3.910   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       2.729   5.237   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.196   5.386   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   36                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11    8                                                       
CONECT   13   11   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   13   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   28                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27   24                                                       
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   38                                                  
CONECT   35   34   36                                                       
CONECT   36   35    4   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   34   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₂N₆O₄S₂

Average Mass

568.7100 Da

Monoisotopic Mass

568.19265 Da

IUPAC Name

(4S,7R,8S,11S,15S,18S)-18-benzyl-7,11-dimethyl-4-(propan-2-yl)-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1^{5,8}.1^{12,15}]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol

Traditional Name

(4S,7R,8S,11S,15S,18S)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1^{5,8}.1^{12,15}]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1N=C(O)C2=CSC(=N2)[C@H](CC2=CC=CC=C2)N=C(O)[C@H]2CSC(=N2)[C@H](C)N=C(O)[C@H]2N=C1O[C@@H]2C

InChI Identifier

InChI=1S/C27H32N6O4S2/c1-13(2)20-25-33-21(15(4)37-25)24(36)28-14(3)26-30-18(11-38-26)22(34)29-17(10-16-8-6-5-7-9-16)27-31-19(12-39-27)23(35)32-20/h5-9,12-15,17-18,20-21H,10-11H2,1-4H3,(H,28,36)(H,29,34)(H,32,35)/t14-,15+,17-,18+,20-,21-/m0/s1

InChI Key

BRLJUCBNCZSZRH-AILWYZJWSA-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
Lissoclinum bistratum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Cyclic peptides

Alternative Parents

Substituents

Cyclic alpha peptide
Monocyclic benzene moiety
Imidothiolactone
Benzenoid
Azole
Heteroaromatic compound
Oxazoline
Thiazole
Meta-thiazoline
Cyclic carboximidic acid
Imido ester
Oxacycle
Polyol
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
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	-0.2	ChemAxon
pKa (Strongest Acidic)	-9.1	ChemAxon
pKa (Strongest Basic)	15.09	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	144.61 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	149.37 m³·mol⁻¹	ChemAxon
Polarizability	58.96 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

163047703

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol (NP0201937)

MOL for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)

3D MOL for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)

3D SDF for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)

3D-SDF for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)

PDB for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)

3D PDB for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)

SMILES for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)

INCHI for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)

Structure for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)

3D Structure for NP0201937 ((4s,7r,8s,11s,15s,18s)-18-benzyl-4-isopropyl-7,11-dimethyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),16,19(22)-heptaene-2,9,16-triol)