NP-MRD: Showing NP-Card for (1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol (NP0257031)

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Record Information

Version

2.0

Created at

2022-09-07 22:02:28 UTC

Updated at

2022-09-07 22:02:28 UTC

NP-MRD ID

NP0257031

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol

Description

Indolizomycin 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,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol is found in Streptomyces griseus. (1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol was first documented in 2021 (PMID: 34402899). Based on a literature review very few articles have been published on Indolizomycin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
    7.1155   -0.2052    0.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7647    0.3839    0.8921 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7316   -0.2699    0.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8495   -1.5794   -0.2819 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3830    0.2836    0.5916 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3080   -0.3242    0.1466 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881    0.2465    0.3246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1242   -0.2941   -0.0873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4409    0.3389    0.1252 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4425    1.8112   -0.2395 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3301    2.7043    0.5319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8923    2.0707   -0.6777 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5522    0.7208   -0.6357 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3629    0.6035   -1.7864 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4352    0.5196    0.5566 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9449   -0.0611    1.7047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7235   -0.8352    0.8240 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0645   -1.9070    0.0174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7598   -1.5547   -0.5686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4671   -0.1859   -0.7275 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.9123    0.5071    1.0114 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2236   -1.1211    1.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1923   -0.5082   -0.3489 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6227    1.3336    1.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8397   -2.0177   -0.1041 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6150   -1.4109   -1.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0985   -2.2913    0.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2478    1.2416    1.1045 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4010   -1.2641   -0.3607 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8953    1.2125    0.8462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0891   -1.2394   -0.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6876    0.2872    1.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6369    2.2075   -0.8820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1141    3.7895    0.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6673    2.3344    1.5322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9868    2.6715   -1.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3064    0.7747   -1.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1814    1.3142    0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6702   -1.1712    1.3160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9190   -2.7883    0.7090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7862   -2.2535   -0.7439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6902   -2.0462   -1.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9135   -2.0285    0.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20  9  1  0
 12 10  1  0
 20 13  1  0
 17 15  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  4 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  6 29  1  0
  7 30  1  0
  8 31  1  0
  9 32  1  1
 10 33  1  6
 11 34  1  0
 11 35  1  0
 12 36  1  6
 14 37  1  0
 15 38  1  1
 17 39  1  1
 18 40  1  0
 18 41  1  0
 19 42  1  0
 19 43  1  0
M  END


  Mrv1652309082200022D          

 20 23  0  0  1  0            999 V2000
   -2.3941   -5.8101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0287   -5.0705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2055   -5.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7476   -5.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8400   -4.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0168   -4.2241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3487   -3.4844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1719   -3.4311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5374   -2.6914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1538   -1.9610    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9304   -1.1668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7299   -1.3705    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4695   -1.7359    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5025   -0.9116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2360   -1.4308    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0025   -1.1256    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8835   -1.9420    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7646   -2.7584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9981   -3.0635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3506   -2.5523    0.0000 N   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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  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
 12 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 17 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  9 20  1  0  0  0  0
 13 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0257031

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C17H23NO2/c1-3-11(2)6-4-5-7-14-12-10-13(12)17(19)16-15(20-16)8-9-18(14)17/h3-7,12-16,19H,8-10H2,1-2H3/b6-4+,7-5+,11-3+/t12-,13+,14+,15-,16-,17+/m1/s1

> <INCHI_KEY>
HLRLKFALZVILBO-HRYKOHBRSA-N

> <FORMULA>
C17H23NO2

> <MOLECULAR_WEIGHT>
273.376

> <EXACT_MASS>
273.172878985

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
31.357599083054016

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,4R,8S,9R,11S)-8-[(1E,3E,5E)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0^{2,4}.0^{9,11}]undecan-1-ol

> <JCHEM_LOGP>
2.438263303

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.018068683791661

> <JCHEM_PKA_STRONGEST_BASIC>
8.16589842310019

> <JCHEM_POLAR_SURFACE_AREA>
36.0

> <JCHEM_REFRACTIVITY>
81.99869999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4R,8S,9R,11S)-8-[(1E,3E,5E)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0^{2,4}.0^{9,11}]undecan-1-ol

> <JCHEM_VEBER_RULE>
1

$$$$

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      -4.469 -10.846   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.787  -9.465   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.250  -9.365   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.396 -10.646   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.568  -7.985   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.031  -7.885   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.651  -6.504   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.188  -6.405   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.870  -5.024   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.154  -3.661   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.737  -2.178   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.229  -2.558   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.610  -3.240   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.671  -1.702   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.041  -2.671   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.471  -2.101   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.249  -3.625   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.027  -5.149   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.596  -5.719   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       4.388  -4.764   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   20                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10   12                                                       
CONECT   12   11   10   13                                                  
CONECT   13   12   14   15   20                                             
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15   17                                                       
CONECT   17   16   15   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    9   13                                                  
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,3S,7R,8R)-7,8-Epoxy-8a-hydroxy-1,2-dimethylene-3-(1E,3E,5E)-(5-methyl-1,3,5-heptatrienyl)octahydroindolizine	MeSH

Chemical Formula

C₁₇H₂₃NO₂

Average Mass

273.3760 Da

Monoisotopic Mass

273.17288 Da

IUPAC Name

(1S,2R,4R,8S,9R,11S)-8-[(1E,3E,5E)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0^{2,4}.0^{9,11}]undecan-1-ol

Traditional Name

(1S,2R,4R,8S,9R,11S)-8-[(1E,3E,5E)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0^{2,4}.0^{9,11}]undecan-1-ol

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C17H23NO2/c1-3-11(2)6-4-5-7-14-12-10-13(12)17(19)16-15(20-16)8-9-18(14)17/h3-7,12-16,19H,8-10H2,1-2H3/b6-4+,7-5+,11-3+/t12-,13+,14+,15-,16-,17+/m1/s1

InChI Key

HLRLKFALZVILBO-HRYKOHBRSA-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
Streptomyces griseus	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
Indolizidine
Para-oxazepine
Epoxypiperidine
Piperidine
N-alkylpyrrolidine
Pyrrolidine
Hemiaminal
Alkanolamine
Dialkyl ether
Oxirane
Ether
Oxacycle
Azacycle
Hydrocarbon derivative
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Organic oxygen 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	2.44	ChemAxon
pKa (Strongest Acidic)	12.02	ChemAxon
pKa (Strongest Basic)	8.17	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	36 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	82 m³·mol⁻¹	ChemAxon
Polarizability	31.36 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

4946175

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6442072

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hotta K: Basic and applied research on multiple aminoglycoside antibiotic resistance of actinomycetes: an old-timer's recollection. J Ind Microbiol Biotechnol. 2021 Dec 23;48(9-10):kuab059. doi: 10.1093/jimb/kuab059. [PubMed:34402899 ]
LOTUS database [Link]

Showing NP-Card for (1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol (NP0257031)

MOL for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)

3D MOL for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)

3D SDF for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)

3D-SDF for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)

PDB for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)

3D PDB for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)

SMILES for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)

INCHI for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)

Structure for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)

3D Structure for NP0257031 ((1s,2r,4r,8s,9r,11s)-8-[(1e,3e,5e)-5-methylhepta-1,3,5-trien-1-yl]-3-oxa-7-azatetracyclo[5.4.0.0²,⁴.0⁹,¹¹]undecan-1-ol)