NP-MRD: Showing NP-Card for Ambiguine L isonitrile (NP0008438)

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Record Information

Version

2.0

Created at

2020-12-09 06:01:46 UTC

Updated at

2021-07-15 17:00:25 UTC

NP-MRD ID

NP0008438

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ambiguine L isonitrile

Provided By

NPAtlas

Description

Ambiguine L isonitrile belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. Ambiguine L isonitrile is found in Fischerella. Based on a literature review very few articles have been published on ambiguine L isonitrile.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106103D          

 59 63  0  0  0  0            999 V2000
   -0.8621   -0.7650   -3.0450 C   0  5  0  0  0  3  0  0  0  0  0  0
   -1.0869   -0.5743   -1.9021 N   0  3  0  0  0  4  0  0  0  0  0  0
   -1.3777   -0.3164   -0.5254 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2941    0.8070   -0.5118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2085    2.0980   -0.3206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0532    2.9227   -0.0294 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0079    4.1970   -0.8808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2304    3.4414    1.4088 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2472    2.2901   -0.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3703    3.0548   -0.2669 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4427    2.2600   -0.2733 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8176    2.4349   -0.4077 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6453    1.3184   -0.3536 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1304    0.0405   -0.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7850   -0.1366   -0.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9833    0.9770   -0.0935 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1072   -0.2534    0.2262 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4143   -0.4024    1.6058 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.2202   -1.0796    0.9934 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1160   -2.7499   -0.8799 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1599   -1.4354    0.1599 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9193   -2.4146   -0.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3880   -1.9917    1.5516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3369    0.4704   -0.7327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1857    2.6142   -0.4002 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6986    5.0666   -0.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0489    4.3505   -1.2391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9934    2.6447    2.1410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2606    3.7884    1.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345    4.2915    1.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4017    4.0892   -0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1912    3.4318   -0.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7169    1.4799   -0.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8012   -0.7641   -0.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  3  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 11 12  2  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  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
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 23 24  1  0  0  0  0
 23 25  1  6  0  0  0
 25 26  2  3  0  0  0
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 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 18  3  1  0  0  0  0
 23  3  1  0  0  0  0
 17  9  2  0  0  0  0
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 27 15  1  0  0  0  0
  4 30  1  0  0  0  0
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  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
  7 34  1  0  0  0  0
  8 35  1  0  0  0  0
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  8 37  1  0  0  0  0
 10 38  1  0  0  0  0
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 29 57  1  0  0  0  0
 29 58  1  0  0  0  0
 29 59  1  0  0  0  0
M  CHG  2   1  -1   2   1
M  END

     RDKit          3D

 59 63  0  0  0  0  0  0  0  0999 V2000
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   -2.2941    0.8070   -0.5118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2085    2.0980   -0.3206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0532    2.9227   -0.0294 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0079    4.1970   -0.8808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2304    3.4414    1.4088 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2472    2.2901   -0.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3703    3.0548   -0.2669 N   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8176    2.4349   -0.4077 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6453    1.3184   -0.3536 C   0  0  0  0  0  0  0  0  0  0  0  0
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 21 22  1  0
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 23 24  1  0
 23 25  1  6
 25 26  2  3
 20 27  1  0
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 27 29  1  0
 18  3  1  0
 23  3  1  0
 17  9  2  0
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 27 15  1  0
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 28 54  1  0
 28 55  1  0
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 29 57  1  0
 29 58  1  0
 29 59  1  0
M  CHG  2   1  -1   2   1
M  END


  Mrv1652306242106103D          

 59 63  0  0  0  0            999 V2000
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    2.1599   -1.4354    0.1599 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9193   -2.4146   -0.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3880   -1.9917    1.5516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3369    0.4704   -0.7327 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3871    4.0248   -1.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6986    5.0666   -0.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0489    4.3505   -1.2391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9934    2.6447    2.1410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2606    3.7884    1.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345    4.2915    1.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4017    4.0892   -0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1912    3.4318   -0.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7169    1.4799   -0.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8012   -0.7641   -0.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1694    0.2021    2.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6962   -1.4093   -1.3351 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0361   -3.4710   -0.7179 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5385   -3.3017    0.9683 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.4882   -2.8173    0.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7394   -2.9063   -0.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3749   -1.8488   -1.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5232   -3.1093    1.5208 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6468   -1.6747    2.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3830   -1.6291    1.9368 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  6  9  1  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
 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  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  6  0  0  0
 25 26  2  3  0  0  0
 20 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 18  3  1  0  0  0  0
 23  3  1  0  0  0  0
 17  9  2  0  0  0  0
 16 11  1  0  0  0  0
 27 15  1  0  0  0  0
  4 30  1  0  0  0  0
  5 31  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
  7 34  1  0  0  0  0
  8 35  1  0  0  0  0
  8 36  1  0  0  0  0
  8 37  1  0  0  0  0
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 22 46  1  0  0  0  0
 22 47  1  0  0  0  0
 24 48  1  0  0  0  0
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 24 50  1  0  0  0  0
 25 51  1  0  0  0  0
 26 52  1  0  0  0  0
 26 53  1  0  0  0  0
 28 54  1  0  0  0  0
 28 55  1  0  0  0  0
 28 56  1  0  0  0  0
 29 57  1  0  0  0  0
 29 58  1  0  0  0  0
 29 59  1  0  0  0  0
M  CHG  2   1  -1   2   1
M  END
> <DATABASE_ID>
NP0008438

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]12C3=C4N([H])C5=C([H])C([H])=C([H])C(=C35)C(C([H])([H])[H])(C([H])([H])[H])[C@@]1([H])C([H])([H])C([H])([H])[C@@](C([H])=C([H])[H])(C([H])([H])[H])[C@@]2([N+]#[C-])C([H])=C([H])C4(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C26H30N2O/c1-8-24(6)13-12-18-23(4,5)16-10-9-11-17-19(16)20-21(28-17)22(2,3)14-15-25(24,27-7)26(18,20)29/h8-11,14-15,18,28-29H,1,12-13H2,2-6H3/t18-,24+,25+,26-/m1/s1

> <INCHI_KEY>
GCEYOMBDTZKZAO-PKNULQPYSA-N

> <FORMULA>
C26H30N2O

> <MOLECULAR_WEIGHT>
386.539

> <EXACT_MASS>
386.235813594

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
44.63990620828188

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(11S,12R,15R,16R)-12-ethenyl-11-isocyano-8,8,12,19,19-pentamethyl-6-azapentacyclo[13.3.1.0^{5,18}.0^{7,17}.0^{11,16}]nonadeca-1(18),2,4,7(17),9-pentaen-16-ol

> <ALOGPS_LOGP>
6.32

> <JCHEM_LOGP>
3.1075296581240557

> <ALOGPS_LOGS>
-5.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.528298244334383

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.085720745239238

> <JCHEM_PKA_STRONGEST_BASIC>
-4.073347399196719

> <JCHEM_POLAR_SURFACE_AREA>
40.379999999999995

> <JCHEM_REFRACTIVITY>
127.38910000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.28e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(11S,12R,15R,16R)-12-ethenyl-11-isocyano-8,8,12,19,19-pentamethyl-6-azapentacyclo[13.3.1.0^{5,18}.0^{7,17}.0^{11,16}]nonadeca-1(18),2,4,7(17),9-pentaen-16-ol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 59 63  0  0  0  0  0  0  0  0999 V2000
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   -0.4143   -0.4024    1.6058 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2028   -1.5390   -0.0623 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2202   -1.0796    0.9934 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2606    3.7884    1.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345    4.2915    1.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1912    3.4318   -0.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7169    1.4799   -0.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8012   -0.7641   -0.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1694    0.2021    2.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6962   -1.4093   -1.3351 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0361   -3.4710   -0.7179 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5385   -3.3017    0.9683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4251   -2.5010    1.7221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9036   -3.5784    0.4203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2014   -0.8399    0.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8066   -0.2976    1.6320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4098   -1.9648    1.6328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6978   -2.1313   -2.2104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7544   -3.2228   -1.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4882   -2.8173    0.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7394   -2.9063   -0.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3749   -1.8488   -1.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5232   -3.1093    1.5208 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6468   -1.6747    2.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3830   -1.6291    1.9368 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0
  3  2  1  6
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  6
 25 26  2  3
 20 27  1  0
 27 28  1  6
 27 29  1  0
 18  3  1  0
 23  3  1  0
 17  9  2  0
 16 11  1  0
 27 15  1  0
  4 30  1  0
  5 31  1  0
  7 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  8 37  1  0
 10 38  1  0
 12 39  1  0
 13 40  1  0
 14 41  1  0
 19 42  1  0
 20 43  1  6
 21 44  1  0
 21 45  1  0
 22 46  1  0
 22 47  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
 25 51  1  0
 26 52  1  0
 26 53  1  0
 28 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
 29 58  1  0
 29 59  1  0
M  CHG  2   1  -1   2   1
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.862  -0.765  -3.045  0.00  0.00           C-1
HETATM    2  N   UNK     0      -1.087  -0.574  -1.902  0.00  0.00           N+1
HETATM    3  C   UNK     0      -1.378  -0.316  -0.525  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.294   0.807  -0.512  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.208   2.098  -0.321  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.053   2.923  -0.029  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.008   4.197  -0.881  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.230   3.441   1.409  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.247   2.290  -0.086  0.00  0.00           C+0
HETATM   10  N   UNK     0       1.370   3.055  -0.267  0.00  0.00           N+0
HETATM   11  C   UNK     0       2.443   2.260  -0.273  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.818   2.435  -0.408  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.645   1.318  -0.354  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.130   0.041  -0.169  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.785  -0.137  -0.037  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.983   0.977  -0.094  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.617   0.981   0.024  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.107  -0.253   0.226  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.414  -0.402   1.606  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.710  -1.475  -0.226  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.014  -2.740   0.145  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.388  -2.586   0.594  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.203  -1.539  -0.062  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.220  -1.080   0.993  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.973  -2.139  -1.173  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.116  -2.750  -0.880  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.160  -1.435   0.160  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.919  -2.415  -0.758  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.388  -1.992   1.552  0.00  0.00           C+0
HETATM   30  H   UNK     0      -3.337   0.470  -0.733  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.186   2.614  -0.400  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.387   4.025  -1.797  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.699   5.067  -0.303  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.049   4.351  -1.239  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.993   2.645   2.141  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.261   3.788   1.575  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.535   4.292   1.584  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.402   4.089  -0.383  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.191   3.432  -0.549  0.00  0.00           H+0
HETATM   40  H   UNK     0       5.717   1.480  -0.461  0.00  0.00           H+0
HETATM   41  H   UNK     0       4.801  -0.764  -0.136  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.169   0.202   2.087  0.00  0.00           H+0
HETATM   43  H   UNK     0       0.696  -1.409  -1.335  0.00  0.00           H+0
HETATM   44  H   UNK     0       0.036  -3.471  -0.718  0.00  0.00           H+0
HETATM   45  H   UNK     0       0.539  -3.302   0.968  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.425  -2.501   1.722  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.904  -3.578   0.420  0.00  0.00           H+0
HETATM   48  H   UNK     0      -4.201  -0.840   0.542  0.00  0.00           H+0
HETATM   49  H   UNK     0      -2.807  -0.298   1.632  0.00  0.00           H+0
HETATM   50  H   UNK     0      -3.410  -1.965   1.633  0.00  0.00           H+0
HETATM   51  H   UNK     0      -2.698  -2.131  -2.210  0.00  0.00           H+0
HETATM   52  H   UNK     0      -4.754  -3.223  -1.632  0.00  0.00           H+0
HETATM   53  H   UNK     0      -4.488  -2.817   0.134  0.00  0.00           H+0
HETATM   54  H   UNK     0       2.227  -3.211  -1.129  0.00  0.00           H+0
HETATM   55  H   UNK     0       3.739  -2.906  -0.236  0.00  0.00           H+0
HETATM   56  H   UNK     0       3.375  -1.849  -1.622  0.00  0.00           H+0
HETATM   57  H   UNK     0       2.523  -3.109   1.521  0.00  0.00           H+0
HETATM   58  H   UNK     0       1.647  -1.675   2.282  0.00  0.00           H+0
HETATM   59  H   UNK     0       3.383  -1.629   1.937  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   18   23                                             
CONECT    4    3    5   30                                                  
CONECT    5    4    6   31                                                  
CONECT    6    5    7    8    9                                             
CONECT    7    6   32   33   34                                             
CONECT    8    6   35   36   37                                             
CONECT    9    6   10   17                                                  
CONECT   10    9   11   38                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13   39                                                  
CONECT   13   12   14   40                                                  
CONECT   14   13   15   41                                                  
CONECT   15   14   16   27                                                  
CONECT   16   15   17   11                                                  
CONECT   17   16   18    9                                                  
CONECT   18   17   19   20    3                                             
CONECT   19   18   42                                                       
CONECT   20   18   21   27   43                                             
CONECT   21   20   22   44   45                                             
CONECT   22   21   23   46   47                                             
CONECT   23   22   24   25    3                                             
CONECT   24   23   48   49   50                                             
CONECT   25   23   26   51                                                  
CONECT   26   25   52   53                                                  
CONECT   27   20   28   29   15                                             
CONECT   28   27   54   55   56                                             
CONECT   29   27   57   58   59                                             
CONECT   30    4                                                            
CONECT   31    5                                                            
CONECT   32    7                                                            
CONECT   33    7                                                            
CONECT   34    7                                                            
CONECT   35    8                                                            
CONECT   36    8                                                            
CONECT   37    8                                                            
CONECT   38   10                                                            
CONECT   39   12                                                            
CONECT   40   13                                                            
CONECT   41   14                                                            
CONECT   42   19                                                            
CONECT   43   20                                                            
CONECT   44   21                                                            
CONECT   45   21                                                            
CONECT   46   22                                                            
CONECT   47   22                                                            
CONECT   48   24                                                            
CONECT   49   24                                                            
CONECT   50   24                                                            
CONECT   51   25                                                            
CONECT   52   26                                                            
CONECT   53   26                                                            
CONECT   54   28                                                            
CONECT   55   28                                                            
CONECT   56   28                                                            
CONECT   57   29                                                            
CONECT   58   29                                                            
CONECT   59   29                                                            
MASTER        0    0    0    0    0    0    0    0   59    0  126    0
END

RDKit          3D

59 63  0  0  0  0  0  0  0  0999 V2000
   -0.8621   -0.7650   -3.0450 C   0  0  0  0  0  3  0  0  0  0  0  0
   -1.0869   -0.5743   -1.9021 N   0  0  0  0  0  4  0  0  0  0  0  0
   -1.3777   -0.3164   -0.5254 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2941    0.8070   -0.5118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2085    2.0980   -0.3206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0532    2.9227   -0.0294 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0079    4.1970   -0.8808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2304    3.4414    1.4088 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2472    2.2901   -0.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3703    3.0548   -0.2669 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4427    2.2600   -0.2733 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8176    2.4349   -0.4077 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6453    1.3184   -0.3536 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1304    0.0405   -0.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7850   -0.1366   -0.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9833    0.9770   -0.0935 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6170    0.9810    0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1072   -0.2534    0.2262 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4143   -0.4024    1.6058 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7098   -1.4754   -0.2262 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0137   -2.7404    0.1445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3876   -2.5857    0.5939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2028   -1.5390   -0.0623 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2202   -1.0796    0.9934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9731   -2.1387   -1.1729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1160   -2.7499   -0.8799 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1599   -1.4354    0.1599 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9193   -2.4146   -0.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3880   -1.9917    1.5516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3369    0.4704   -0.7327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1857    2.6142   -0.4002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3871    4.0248   -1.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6986    5.0666   -0.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0489    4.3505   -1.2391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9934    2.6447    2.1410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2606    3.7884    1.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345    4.2915    1.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4017    4.0892   -0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1912    3.4318   -0.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7169    1.4799   -0.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8012   -0.7641   -0.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1694    0.2021    2.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6962   -1.4093   -1.3351 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0361   -3.4710   -0.7179 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5385   -3.3017    0.9683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4251   -2.5010    1.7221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9036   -3.5784    0.4203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2014   -0.8399    0.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8066   -0.2976    1.6320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4098   -1.9648    1.6328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6978   -2.1313   -2.2104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7544   -3.2228   -1.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4882   -2.8173    0.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2271   -3.2110   -1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7394   -2.9063   -0.2360 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3749   -1.8488   -1.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5232   -3.1093    1.5208 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6468   -1.6747    2.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3830   -1.6291    1.9368 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0
  3  2  1  6
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  6
 25 26  2  3
 20 27  1  0
 27 28  1  6
 27 29  1  0
 18  3  1  0
 23  3  1  0
 17  9  2  0
 16 11  1  0
 27 15  1  0
  4 30  1  0
  5 31  1  0
  7 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  8 37  1  0
 10 38  1  0
 12 39  1  0
 13 40  1  0
 14 41  1  0
 19 42  1  0
 20 43  1  6
 21 44  1  0
 21 45  1  0
 22 46  1  0
 22 47  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
 25 51  1  0
 26 52  1  0
 26 53  1  0
 28 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
 29 58  1  0
 29 59  1  0
M  CHG  2   1  -1   2   1
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₆H₃₀N₂O

Average Mass

386.5390 Da

Monoisotopic Mass

386.23581 Da

IUPAC Name

(11S,12R,15R,16R)-12-ethenyl-11-isocyano-8,8,12,19,19-pentamethyl-6-azapentacyclo[13.3.1.0^{5,18}.0^{7,17}.0^{11,16}]nonadeca-1(18),2,4,7(17),9-pentaen-16-ol

Traditional Name

(11S,12R,15R,16R)-12-ethenyl-11-isocyano-8,8,12,19,19-pentamethyl-6-azapentacyclo[13.3.1.0^{5,18}.0^{7,17}.0^{11,16}]nonadeca-1(18),2,4,7(17),9-pentaen-16-ol

CAS Registry Number

Not Available

SMILES

CC1(C)[C@H]2CC[C@](C)(C=C)[C@]3(C=CC(C)(C)C4=C(C5=C1C=CC=C5N4)[C@]23O)[N+]#[C-]

InChI Identifier

InChI=1S/C26H30N2O/c1-8-24(6)13-12-18-23(4,5)16-10-9-11-17-19(16)20-21(28-17)22(2,3)14-15-25(24,27-7)26(18,20)29/h8-11,14-15,18,28-29H,1,12-13H2,2-6H3/t18-,24+,25+,26-/m1/s1

InChI Key

GCEYOMBDTZKZAO-PKNULQPYSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Fischerella	NPAtlas	19371071

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Isoindole or derivatives
Benzenoid
Heteroaromatic compound
Tertiary alcohol
Pyrrole
Cyclic alcohol
Azacycle
Organic isocyanide
Organopnictogen compound
Hydrocarbon derivative
Organic zwitterion
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Alcohol
Organic oxygen 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	6.32	ALOGPS
logP	3.11	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	12.09	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.38 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	127.39 m³·mol⁻¹	ChemAxon
Polarizability	44.64 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA014388

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

24629294

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44139241

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Ambiguine L isonitrile (NP0008438)

MOL for NP0008438 (Ambiguine L isonitrile)

3D MOL for NP0008438 (Ambiguine L isonitrile)

3D SDF for NP0008438 (Ambiguine L isonitrile)

3D-SDF for NP0008438 (Ambiguine L isonitrile)

PDB for NP0008438 (Ambiguine L isonitrile)

3D PDB for NP0008438 (Ambiguine L isonitrile)

SMILES for NP0008438 (Ambiguine L isonitrile)

INCHI for NP0008438 (Ambiguine L isonitrile)

Structure for NP0008438 (Ambiguine L isonitrile)

3D Structure for NP0008438 (Ambiguine L isonitrile)