NP-MRD: Showing NP-Card for myrioneurinol (NP0025143)

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Record Information

Version

2.0

Created at

2021-06-19 17:20:13 UTC

Updated at

2021-06-29 23:49:53 UTC

NP-MRD ID

NP0025143

Secondary Accession Numbers

None

Natural Product Identification

Common Name

myrioneurinol

Provided By

JEOL Database JEOL Logo

Description

[(1R,9R,11S,12R,17S)-7-oxa-5-azatetracyclo[7.7.1.0¹,¹².0⁵,¹⁷]Heptadecan-11-yl]methanol belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom. myrioneurinol is found in Myrioneuron nutans. myrioneurinol was first documented in 2007 (Pham, V. C., et al.). Based on a literature review very few articles have been published on [(1R,9R,11S,12R,17S)-7-oxa-5-azatetracyclo[7.7.1.0¹,¹².0⁵,¹⁷]Heptadecan-11-yl]methanol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192119203D          

 46 49  0  0  0  0            999 V2000
   -1.1985   -0.4103    3.9182 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9765   -0.6283    2.7504 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1930   -0.2251    1.4888 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9844    1.3039    1.4913 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2617    1.7773    0.2327 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0243    3.2861    0.2430 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6507    3.6753   -0.9528 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9123    3.0232   -1.0775 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7972    1.5663   -1.1472 N   0  0  2  0  0  0  0  0  0  0  0  0
    1.1593    1.1551   -2.4040 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9799   -0.3602   -2.4923 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2811   -0.9323   -1.2573 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9737   -0.4880    0.0641 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3964   -1.1234    0.1677 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3689   -2.6463    0.2972 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4913   -3.1057    1.4539 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1020   -2.4679    1.4445 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1842   -0.9323    1.3479 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0974    1.0674    0.0523 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7342   -0.6996    4.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8945   -0.0360    2.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2703   -1.6816    2.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8253   -0.4875    0.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4134    1.6053    2.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9576    1.8064    1.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9118    1.5559   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9786    3.8223    0.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5616    3.6052    1.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5561    3.3183   -0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4020    3.4106   -1.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7857    1.4692   -3.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1849    1.6379   -2.5466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9545   -0.8422   -2.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3915   -0.6031   -3.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2421   -2.0216   -1.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7629   -0.6023   -1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9094   -0.7141    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3902   -3.0146    0.4508 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195   -3.1009   -0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3958   -4.1973    1.4335 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9897   -2.8535    2.3986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3986   -2.7713    2.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4949   -2.8750    0.6210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7840   -0.6062    2.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7223    1.3353    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0  0  0  0
  5  6  1  0  0  0  0
 19  9  1  0  0  0  0
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  8  7  1  0  0  0  0
  7  6  1  0  0  0  0
 13 18  1  0  0  0  0
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  5  4  1  0  0  0  0
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  4  3  1  0  0  0  0
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 17 43  1  0  0  0  0
 17 44  1  0  0  0  0
  2 21  1  0  0  0  0
  2 22  1  0  0  0  0
  1 20  1  0  0  0  0
M  END

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -1.1985   -0.4103    3.9182 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9765   -0.6283    2.7504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1930   -0.2251    1.4888 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9844    1.3039    1.4913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2617    1.7773    0.2327 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0243    3.2861    0.2430 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6507    3.6753   -0.9528 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9123    3.0232   -1.0775 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7972    1.5663   -1.1472 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1593    1.1551   -2.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9799   -0.3602   -2.4923 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2811   -0.9323   -1.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9737   -0.4880    0.0641 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3964   -1.1234    0.1677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3689   -2.6463    0.2972 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913   -3.1057    1.4539 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1020   -2.4679    1.4445 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -0.9323    1.3479 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0974    1.0674    0.0523 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7342   -0.6996    4.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2703   -1.6816    2.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8253   -0.4875    0.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4134    1.6053    2.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9576    1.8064    1.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9118    1.5559   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9786    3.8223    0.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5616    3.6052    1.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5561    3.3183   -0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4020    3.4106   -1.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7857    1.4692   -3.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1849    1.6379   -2.5466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9545   -0.8422   -2.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3915   -0.6031   -3.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2421   -2.0216   -1.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7629   -0.6023   -1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0245   -0.8540   -0.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0195   -3.1009   -0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7223    1.3353    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 20  1  0
M  END


  Mrv1652306192119203D          

 46 49  0  0  0  0            999 V2000
   -1.1985   -0.4103    3.9182 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9765   -0.6283    2.7504 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1930   -0.2251    1.4888 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9844    1.3039    1.4913 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2617    1.7773    0.2327 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0243    3.2861    0.2430 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6507    3.6753   -0.9528 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9123    3.0232   -1.0775 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7972    1.5663   -1.1472 N   0  0  2  0  0  0  0  0  0  0  0  0
    1.1593    1.1551   -2.4040 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.3689   -2.6463    0.2972 C   0  0  2  0  0  0  0  0  0  0  0  0
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 14 37  1  0  0  0  0
 14 38  1  0  0  0  0
 15 39  1  0  0  0  0
 15 40  1  0  0  0  0
 16 41  1  0  0  0  0
 16 42  1  0  0  0  0
 17 43  1  0  0  0  0
 17 44  1  0  0  0  0
  2 21  1  0  0  0  0
  2 22  1  0  0  0  0
  1 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0025143

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@@]1([H])C([H])([H])[C@@]2([H])C([H])([H])OC([H])([H])N3C([H])([H])C([H])([H])C([H])([H])[C@@]4(C([H])([H])C([H])([H])C([H])([H])C([H])([H])[C@]14[H])[C@]23[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H27NO2/c18-9-12-8-13-10-19-11-17-7-3-6-16(15(13)17)5-2-1-4-14(12)16/h12-15,18H,1-11H2/t12-,13+,14-,15+,16-/m1/s1

> <INCHI_KEY>
RXMOFQMQVNFTLE-DGADGQDISA-N

> <FORMULA>
C16H27NO2

> <MOLECULAR_WEIGHT>
265.397

> <EXACT_MASS>
265.204179113

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
30.46520995277689

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,9R,11S,12R,17S)-7-oxa-5-azatetracyclo[7.7.1.0^{1,12}.0^{5,17}]heptadecan-11-yl]methanol

> <ALOGPS_LOGP>
1.80

> <JCHEM_LOGP>
1.8957276283333337

> <ALOGPS_LOGS>
-2.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.036751112761774

> <JCHEM_PKA_STRONGEST_BASIC>
7.639122039545999

> <JCHEM_POLAR_SURFACE_AREA>
32.7

> <JCHEM_REFRACTIVITY>
74.98329999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.04e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,9R,11S,12R,17S)-7-oxa-5-azatetracyclo[7.7.1.0^{1,12}.0^{5,17}]heptadecan-11-ylmethanol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -1.1985   -0.4103    3.9182 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9765   -0.6283    2.7504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1930   -0.2251    1.4888 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9844    1.3039    1.4913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2617    1.7773    0.2327 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0243    3.2861    0.2430 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6507    3.6753   -0.9528 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9123    3.0232   -1.0775 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7972    1.5663   -1.1472 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1593    1.1551   -2.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9799   -0.3602   -2.4923 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2811   -0.9323   -1.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9737   -0.4880    0.0641 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3964   -1.1234    0.1677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3689   -2.6463    0.2972 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913   -3.1057    1.4539 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1020   -2.4679    1.4445 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -0.9323    1.3479 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0974    1.0674    0.0523 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7342   -0.6996    4.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8945   -0.0360    2.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2703   -1.6816    2.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8253   -0.4875    0.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4134    1.6053    2.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9576    1.8064    1.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9118    1.5559   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9786    3.8223    0.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5616    3.6052    1.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5561    3.3183   -0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4020    3.4106   -1.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7857    1.4692   -3.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1849    1.6379   -2.5466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9545   -0.8422   -2.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3915   -0.6031   -3.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2421   -2.0216   -1.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7629   -0.6023   -1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0245   -0.8540   -0.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9094   -0.7141    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3902   -3.0146    0.4508 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195   -3.1009   -0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3958   -4.1973    1.4335 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9897   -2.8535    2.3986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3986   -2.7713    2.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4949   -2.8750    0.6210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7840   -0.6062    2.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7223    1.3353    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  5  6  1  0
 19  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
 13 18  1  0
 19 46  1  1
  5  4  1  0
 13 14  1  1
  4  3  1  0
 14 15  1  0
  3 18  1  0
 15 16  1  0
  5 19  1  0
 16 17  1  0
 17 18  1  0
 13 12  1  0
 18 45  1  1
 13 19  1  0
  3  2  1  0
 11 10  1  0
  2  1  1  0
  3 23  1  6
 11 12  1  0
  5 26  1  6
 11 33  1  0
 11 34  1  0
 10 31  1  0
 10 32  1  0
 12 35  1  0
 12 36  1  0
  4 24  1  0
  4 25  1  0
  8 29  1  0
  8 30  1  0
  6 27  1  0
  6 28  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 17 44  1  0
  2 21  1  0
  2 22  1  0
  1 20  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  O   UNK     0      -1.198  -0.410   3.918  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.976  -0.628   2.750  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.193  -0.225   1.489  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.984   1.304   1.491  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.262   1.777   0.233  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.024   3.286   0.243  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.651   3.675  -0.953  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.912   3.023  -1.077  0.00  0.00           C+0
HETATM    9  N   UNK     0       1.797   1.566  -1.147  0.00  0.00           N+0
HETATM   10  C   UNK     0       1.159   1.155  -2.404  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.980  -0.360  -2.492  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.281  -0.932  -1.257  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.974  -0.488   0.064  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.396  -1.123   0.168  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.369  -2.646   0.297  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.491  -3.106   1.454  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.102  -2.468   1.444  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.184  -0.932   1.348  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.097   1.067   0.052  0.00  0.00           C+0
HETATM   20  H   UNK     0      -1.734  -0.700   4.677  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.894  -0.036   2.834  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.270  -1.682   2.714  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.825  -0.488   0.632  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.413   1.605   2.379  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.958   1.806   1.559  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.912   1.556  -0.623  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.979   3.822   0.274  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.562   3.605   1.114  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.556   3.318  -0.239  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.402   3.411  -1.978  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.786   1.469  -3.248  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.185   1.638  -2.547  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.954  -0.842  -2.631  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.392  -0.603  -3.385  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.242  -2.022  -1.352  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.763  -0.602  -1.278  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.025  -0.854  -0.688  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.909  -0.714   1.049  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.390  -3.015   0.451  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.019  -3.101  -0.636  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.396  -4.197   1.434  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.990  -2.853   2.399  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.399  -2.771   2.370  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.495  -2.875   0.621  0.00  0.00           H+0
HETATM   45  H   UNK     0       0.784  -0.606   2.212  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.722   1.335   0.919  0.00  0.00           H+0
CONECT    1    2   20                                                       
CONECT    2    3    1   21   22                                             
CONECT    3    4   18    2   23                                             
CONECT    4    5    3   24   25                                             
CONECT    5    6    4   19   26                                             
CONECT    6    5    7   27   28                                             
CONECT    7    8    6                                                       
CONECT    8    9    7   29   30                                             
CONECT    9   10   19    8                                                  
CONECT   10    9   11   31   32                                             
CONECT   11   10   12   33   34                                             
CONECT   12   13   11   35   36                                             
CONECT   13   18   14   12   19                                             
CONECT   14   13   15   37   38                                             
CONECT   15   14   16   39   40                                             
CONECT   16   15   17   41   42                                             
CONECT   17   16   18   43   44                                             
CONECT   18   13    3   17   45                                             
CONECT   19    9   46    5   13                                             
CONECT   20    1                                                            
CONECT   21    2                                                            
CONECT   22    2                                                            
CONECT   23    3                                                            
CONECT   24    4                                                            
CONECT   25    4                                                            
CONECT   26    5                                                            
CONECT   27    6                                                            
CONECT   28    6                                                            
CONECT   29    8                                                            
CONECT   30    8                                                            
CONECT   31   10                                                            
CONECT   32   10                                                            
CONECT   33   11                                                            
CONECT   34   11                                                            
CONECT   35   12                                                            
CONECT   36   12                                                            
CONECT   37   14                                                            
CONECT   38   14                                                            
CONECT   39   15                                                            
CONECT   40   15                                                            
CONECT   41   16                                                            
CONECT   42   16                                                            
CONECT   43   17                                                            
CONECT   44   17                                                            
CONECT   45   18                                                            
CONECT   46   19                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   98    0
END

RDKit          3D

46 49  0  0  0  0  0  0  0  0999 V2000
   -1.1985   -0.4103    3.9182 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9765   -0.6283    2.7504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1930   -0.2251    1.4888 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9844    1.3039    1.4913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2617    1.7773    0.2327 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0243    3.2861    0.2430 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6507    3.6753   -0.9528 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9123    3.0232   -1.0775 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7972    1.5663   -1.1472 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1593    1.1551   -2.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9799   -0.3602   -2.4923 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2811   -0.9323   -1.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9737   -0.4880    0.0641 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3964   -1.1234    0.1677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3689   -2.6463    0.2972 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913   -3.1057    1.4539 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1020   -2.4679    1.4445 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -0.9323    1.3479 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0974    1.0674    0.0523 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7342   -0.6996    4.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8945   -0.0360    2.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2703   -1.6816    2.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8253   -0.4875    0.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4134    1.6053    2.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9576    1.8064    1.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9118    1.5559   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9786    3.8223    0.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5616    3.6052    1.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5561    3.3183   -0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4020    3.4106   -1.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7857    1.4692   -3.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1849    1.6379   -2.5466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9545   -0.8422   -2.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3915   -0.6031   -3.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2421   -2.0216   -1.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7629   -0.6023   -1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0245   -0.8540   -0.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9094   -0.7141    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3902   -3.0146    0.4508 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195   -3.1009   -0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3958   -4.1973    1.4335 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9897   -2.8535    2.3986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3986   -2.7713    2.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4949   -2.8750    0.6210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7840   -0.6062    2.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7223    1.3353    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  5  6  1  0
 19  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
 13 18  1  0
 19 46  1  1
  5  4  1  0
 13 14  1  1
  4  3  1  0
 14 15  1  0
  3 18  1  0
 15 16  1  0
  5 19  1  0
 16 17  1  0
 17 18  1  0
 13 12  1  0
 18 45  1  1
 13 19  1  0
  3  2  1  0
 11 10  1  0
  2  1  1  0
  3 23  1  6
 11 12  1  0
  5 26  1  6
 11 33  1  0
 11 34  1  0
 10 31  1  0
 10 32  1  0
 12 35  1  0
 12 36  1  0
  4 24  1  0
  4 25  1  0
  8 29  1  0
  8 30  1  0
  6 27  1  0
  6 28  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 17 44  1  0
  2 21  1  0
  2 22  1  0
  1 20  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₇NO₂

Average Mass

265.3970 Da

Monoisotopic Mass

265.20418 Da

IUPAC Name

[(1R,9R,11S,12R,17S)-7-oxa-5-azatetracyclo[7.7.1.0^{1,12}.0^{5,17}]heptadecan-11-yl]methanol

Traditional Name

(1R,9R,11S,12R,17S)-7-oxa-5-azatetracyclo[7.7.1.0^{1,12}.0^{5,17}]heptadecan-11-ylmethanol

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@@]1([H])C([H])([H])[C@@]2([H])C([H])([H])OC([H])([H])N3C([H])([H])C([H])([H])C([H])([H])[C@@]4(C([H])([H])C([H])([H])C([H])([H])C([H])([H])[C@]14[H])[C@]23[H]

InChI Identifier

InChI=1S/C16H27NO2/c18-9-12-8-13-10-19-11-17-7-3-6-16(15(13)17)5-2-1-4-14(12)16/h12-15,18H,1-11H2/t12-,13+,14-,15+,16-/m1/s1

InChI Key

RXMOFQMQVNFTLE-DGADGQDISA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Mycetia nutans	JEOL database	Pham, V. C., et al, Tetrahedron 63, 11244 (2007)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azaspirodecane derivatives

Sub Class

Not Available

Direct Parent

Azaspirodecane derivatives

Alternative Parents

Substituents

Azaspirodecane
Quinolidine
1,3-oxazinane
Oxazinane
Piperidine
Hemiaminal
Azacycle
Oxacycle
Organic oxygen compound
Primary alcohol
Alcohol
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Amine
Hydrocarbon derivative
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	1.8	ALOGPS
logP	1.9	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	18.04	ChemAxon
pKa (Strongest Basic)	7.64	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	32.7 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	74.98 m³·mol⁻¹	ChemAxon
Polarizability	30.47 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

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

24770588

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pham, V. C., et al. (2007). Pham, V. C., et al, Tetrahedron 63, 11244 (2007). Tetrahedron.

Showing NP-Card for myrioneurinol (NP0025143)

MOL for NP0025143 (myrioneurinol)

3D MOL for NP0025143 (myrioneurinol)

3D SDF for NP0025143 (myrioneurinol)

3D-SDF for NP0025143 (myrioneurinol)

PDB for NP0025143 (myrioneurinol)

3D PDB for NP0025143 (myrioneurinol)

SMILES for NP0025143 (myrioneurinol)

INCHI for NP0025143 (myrioneurinol)

Structure for NP0025143 (myrioneurinol)

3D Structure for NP0025143 (myrioneurinol)