NP-MRD: Showing NP-Card for (2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine (NP0183451)

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Record Information

Version

2.0

Created at

2022-09-03 22:21:41 UTC

Updated at

2022-09-03 22:21:41 UTC

NP-MRD ID

NP0183451

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine

Description

Eudistomin belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety. (2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine was first documented in 2019 (PMID: 31339328). Based on a literature review a small amount of articles have been published on Eudistomin (PMID: 33339375) (PMID: 33349820) (PMID: 34972183).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 39  0  0  0  0  0  0  0  0999 V2000
   -1.6317    2.2966    0.3675 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0169    1.3482   -0.6625 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4840    1.1351   -0.5398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9607   -0.6140   -0.6540 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5150   -1.3513    0.9717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1948   -0.8676    1.1717 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6032   -0.9959    0.0042 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -2.1161    0.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4270   -2.0177   -0.9394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1121   -0.7428   -0.5791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2629    0.3687   -0.4651 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0473    1.4053   -0.1405 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3288    0.9992   -0.0476 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5085    1.6534    0.2521 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7119    0.9361    0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7662   -0.4146   -0.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5678   -1.0783   -0.3088 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3994   -0.3576   -0.3205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1790    0.1268   -0.7175 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2259    2.2020    1.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5311    3.2581    0.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8845    1.9198   -1.6329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0734    1.7525   -1.2550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8251    1.4697    0.4648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5093   -2.4512    0.8269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1916   -1.0185    1.7567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3234   -3.0303   -0.2332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3085   -2.2313    1.0337 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1014   -2.8560   -0.7199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0640   -2.0130   -1.9867 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6957    2.3635    0.0093 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4834    2.7102    0.4688 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6204    1.4817    0.5088 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7203   -0.9180    0.0227 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5901   -2.1371   -0.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2064   -0.2158   -1.8051 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 11 19  1  0
 19  2  1  0
 19  7  1  0
 18 10  1  0
 18 13  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  6
  3 23  1  0
  3 24  1  0
  5 25  1  0
  5 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
  9 30  1  0
 12 31  1  0
 14 32  1  0
 15 33  1  0
 16 34  1  0
 17 35  1  0
 19 36  1  6
M  END


  Mrv1652309042200212D          

 19 22  0  0  1  0            999 V2000
    1.9646   -0.9751    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4498   -0.3304    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6456   -0.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0003   -0.0005    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0003    0.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6444    1.3392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4489    1.1562    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9132    1.8381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7359    1.7769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0943    1.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6300    0.3519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1351   -0.3004    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9116   -0.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6383   -0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3398    0.0220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3146    0.8466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5879    1.2371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8864    0.8030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8073    0.4131    0.0000 C   0  0  2  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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  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
 10 18  1  0  0  0  0
 13 18  1  0  0  0  0
 19 11  1  6  0  0  0
  2 19  1  0  0  0  0
  7 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0183451

> <DATABASE_NAME>
NP-MRD

> <SMILES>
N[C@@H]1CSCON2CCC3=C(NC4=CC=CC=C34)[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C14H17N3OS/c15-11-7-19-8-18-17-6-5-10-9-3-1-2-4-12(9)16-13(10)14(11)17/h1-4,11,14,16H,5-8,15H2/t11-,14+/m1/s1

> <INCHI_KEY>
SFAMFXNCPDEYGA-RISCZKNCSA-N

> <FORMULA>
C14H17N3OS

> <MOLECULAR_WEIGHT>
275.37

> <EXACT_MASS>
275.109233353

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
30.043028806514872

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0^{2,8}.0^{12,17}]octadeca-1(11),12,14,16-tetraen-3-amine

> <JCHEM_LOGP>
1.1751108786666669

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.262316300854536

> <JCHEM_PKA_STRONGEST_BASIC>
8.78504963991452

> <JCHEM_POLAR_SURFACE_AREA>
54.28

> <JCHEM_REFRACTIVITY>
77.41749999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0^{2,8}.0^{12,17}]octadeca-1(11),12,14,16-tetraen-3-amine

> <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  N   UNK     0       3.667  -1.820   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       2.706  -0.617   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.205  -0.960   0.000  0.00  0.00           C+0
HETATM    4  S   UNK     0       0.000  -0.001   0.000  0.00  0.00           S+0
HETATM    5  C   UNK     0      -0.000   1.539   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.203   2.500   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0       2.705   2.158   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       3.571   3.431   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.107   3.317   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.776   1.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.909   0.657   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       5.852  -0.561   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       7.302  -0.040   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.658  -0.769   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.968   0.041   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.921   1.580   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.564   2.309   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.255   1.499   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.374   0.771   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   18                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   10   13                                                  
CONECT   19   11    2    7                                                  
MASTER        0    0    0    0    0    0    0    0   19    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₇N₃OS

Average Mass

275.3700 Da

Monoisotopic Mass

275.10923 Da

IUPAC Name

(2S,3S)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0^{2,8}.0^{12,17}]octadeca-1(11),12,14,16-tetraen-3-amine

Traditional Name

(2S,3S)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0^{2,8}.0^{12,17}]octadeca-1(11),12,14,16-tetraen-3-amine

CAS Registry Number

Not Available

SMILES

N[C@@H]1CSCON2CCC3=C(NC4=CC=CC=C34)[C@H]12

InChI Identifier

InChI=1S/C14H17N3OS/c15-11-7-19-8-18-17-6-5-10-9-3-1-2-4-12(9)16-13(10)14(11)17/h1-4,11,14,16H,5-8,15H2/t11-,14+/m1/s1

InChI Key

SFAMFXNCPDEYGA-RISCZKNCSA-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 beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Beta carbolines

Alternative Parents

Substituents

Beta-carboline
3-alkylindole
Indole
Aralkylamine
Benzenoid
Pyrrole
Heteroaromatic compound
Oxacycle
Azacycle
N-organohydroxylamine
Hydrocarbon derivative
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Organic oxygen compound
Amine
Organic nitrogen 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	1.18	ChemAxon
pKa (Strongest Acidic)	16.26	ChemAxon
pKa (Strongest Basic)	8.79	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	54.28 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	77.42 m³·mol⁻¹	ChemAxon
Polarizability	30.04 Å³	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00026548

Chemspider ID

2279125

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Eudistomin

METLIN ID

Not Available

PubChem Compound

3009848

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ahmad R, Lim CK, Marzuki NF, Goh YK, Azizan KA, Goh YK, Goh KJ, Ramzi AB, Baharum SN: Metabolic Profile of Scytalidium parasiticum-Ganoderma boninense Co-Cultures Revealed the Alkaloids, Flavonoids and Fatty Acids that Contribute to Anti-Ganoderma Activity. Molecules. 2020 Dec 16;25(24). pii: molecules25245965. doi: 10.3390/molecules25245965. [PubMed:33339375 ]
Ranjani G, Nagarajan R: Access to 1-indolyltetrahydro-beta-carbolines via metal-free cross-dehydrogenative coupling: the total synthesis of eudistomin U, isoeudistomin U and 19-bromoisoeudistomin U. Chem Commun (Camb). 2021 Jan 18;57(6):757-760. doi: 10.1039/d0cc06958b. Epub 2020 Dec 22. [PubMed:33349820 ]
Ong CE, Ahmad R, Goh YK, Azizan KA, Baharum SN, Goh KJ: Growth modulation and metabolic responses of Ganoderma boninense to salicylic acid stress. PLoS One. 2021 Dec 31;16(12):e0262029. doi: 10.1371/journal.pone.0262029. eCollection 2021. [PubMed:34972183 ]
Xu D, Ye F, Ye J, Gao Y, Chen H: Manipulation of Water for Diversified Functionalization of Tetrahydro-beta-carbolines (THbetaCs) with Indoles. Org Lett. 2019 Aug 2;21(15):6160-6163. doi: 10.1021/acs.orglett.9b02413. Epub 2019 Jul 24. [PubMed:31339328 ]
LOTUS database [Link]

Showing NP-Card for (2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine (NP0183451)

MOL for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)

3D MOL for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)

3D SDF for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)

3D-SDF for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)

PDB for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)

3D PDB for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)

SMILES for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)

INCHI for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)

Structure for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)

3D Structure for NP0183451 ((2s,3s)-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine)