NP-MRD: Showing NP-Card for 9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one (NP0282125)

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Record Information

Version

2.0

Created at

2022-09-09 08:50:25 UTC

Updated at

2022-09-09 08:50:26 UTC

NP-MRD ID

NP0282125

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one

Description

9-Hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]Docos-13-en-4-one belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring. 9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one is found in Daphniphyllum oldhamii. Based on a literature review very few articles have been published on 9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]Docos-13-en-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092210502D          

 26 31  0  0  0  0            999 V2000
    3.2693    4.9240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1198    4.1126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6883    3.5148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2953    2.7893    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5715    2.0119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3828    1.8624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0368    2.3653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7172    1.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4837    1.1074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6590    1.0850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1238    0.4571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4000   -0.3203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3125    0.6067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0363    1.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2250    1.5336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011    0.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6898    0.9057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8785    1.0553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3433    0.4274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6023    1.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468    2.3442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9488    2.3110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1863    2.6260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2502    3.4485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3755    3.7567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4840    2.9389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
  4 26  1  0  0  0  0
 22 26  1  0  0  0  0
M  END

     RDKit          3D

 57 62  0  0  0  0  0  0  0  0999 V2000
   -1.5168   -3.4444    1.8279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2992   -2.7671    0.4779 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1088   -2.2915    0.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0951   -0.8459    0.3865 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6998   -0.3597   -0.8174 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1705   -0.7105   -0.7256 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0214   -1.3359   -1.4856 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3838   -1.4021   -0.9053 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3141   -0.3498    0.2031 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8386   -0.2557    0.4954 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3844    1.1392    0.8329 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5179    1.8529    1.2254 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7718    1.8662   -0.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6324    1.1308   -0.9808 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7111    1.7160   -0.6360 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3228    2.4788   -1.8200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4992    2.6884    0.3651 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4303    3.0973    1.2711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3818    4.2746    1.7057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4614    2.1122    1.6967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8811    1.3368    0.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7306    0.6888   -0.2367 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3693    0.0317   -1.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6687   -1.3766   -1.0590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1648   -1.5554    0.3565 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2195   -0.4015    0.6247 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4716   -4.0106    1.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5982   -2.6245    2.5705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6877   -4.1360    2.0430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5941   -3.4941   -0.3259 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7501   -2.7181    1.1231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4964   -2.6722   -0.6363 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3237   -0.9218   -1.6903 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458   -1.7667   -2.4564 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0829   -0.9935   -1.6619 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6633   -2.3833   -0.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.8889   -0.7001    1.0785 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6136   -0.9266    1.3287 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7052    1.1111    1.7169 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4450    2.2159    2.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4659    2.8678    0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7706    1.3056   -2.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4070    2.4330   -1.8308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8739    1.9805   -2.7287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0144    3.5415   -1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3297    2.7067    2.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1155    1.5207    2.5564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4823    1.9970   -0.1529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5769    0.4907    0.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7305    0.1239   -2.3579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3371    0.5171   -1.7233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2695   -2.1413   -1.7434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7796   -1.5752   -1.0093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9764   -1.6008    1.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3291   -0.1578    1.7056 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 26  1  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 22 23  1  6
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
 18 17  1  0
 17 15  1  0
 15 16  1  6
 15 14  1  0
 14 13  1  0
 13 11  1  0
 11 12  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
 25  2  1  0
 15 22  1  0
  5 14  1  0
  5  4  1  0
 22 26  1  0
  6 10  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  6
  3 31  1  0
  3 32  1  0
 26 57  1  1
 25 56  1  1
 24 54  1  0
 24 55  1  0
 23 52  1  0
 23 53  1  0
 21 50  1  0
 21 51  1  0
 20 48  1  0
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 16 45  1  0
 16 46  1  0
 16 47  1  0
 14 44  1  6
 13 42  1  0
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 10 39  1  1
  9 37  1  0
  9 38  1  0
  8 35  1  0
  8 36  1  0
  7 34  1  0
  5 33  1  6
M  END


  Mrv1652309092210502D          

 26 31  0  0  0  0            999 V2000
    3.2693    4.9240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1198    4.1126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6883    3.5148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2953    2.7893    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5715    2.0119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3828    1.8624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0368    2.3653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7172    1.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4837    1.1074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6590    1.0850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1238    0.4571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4000   -0.3203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3125    0.6067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0363    1.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2250    1.5336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011    0.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6898    0.9057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8785    1.0553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3433    0.4274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6023    1.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468    2.3442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9488    2.3110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1863    2.6260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2502    3.4485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3755    3.7567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4840    2.9389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
  4 26  1  0  0  0  0
 22 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0282125

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CN2C3C1CCC31CCC(=O)OC1(C)C1CC(O)C3CCC=C3C21

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO3/c1-12-11-23-19-15-5-3-4-14(15)17(24)10-16(19)21(2)22(9-7-18(25)26-21)8-6-13(12)20(22)23/h5,12-14,16-17,19-20,24H,3-4,6-11H2,1-2H3

> <INCHI_KEY>
YCFFNWSZGGOQEQ-UHFFFAOYSA-N

> <FORMULA>
C22H31NO3

> <MOLECULAR_WEIGHT>
357.494

> <EXACT_MASS>
357.230393862

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
39.97152382141042

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-4-one

> <JCHEM_LOGP>
2.121339723333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.866616656011477

> <JCHEM_PKA_STRONGEST_BASIC>
11.453989279200062

> <JCHEM_POLAR_SURFACE_AREA>
49.77

> <JCHEM_REFRACTIVITY>
99.17979999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       6.103   9.191   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.824   7.677   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.885   6.561   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       6.151   5.207   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       6.667   3.756   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.181   3.476   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.402   4.415   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.672   3.544   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.236   2.067   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.697   2.025   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.698   0.853   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.213  -0.598   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.183   1.132   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.668   2.584   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.153   2.863   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.669   1.412   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.154   1.691   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.640   1.970   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.641   0.798   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.124   3.421   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.141   4.376   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.638   4.314   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.214   4.902   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.334   6.437   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.434   7.013   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.637   5.486   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   26                                                  
CONECT    5    4    6   14                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6   11                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    5   15                                                  
CONECT   15   14   16   17   22                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   15   23   26                                             
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    2   26                                                  
CONECT   26   25    4   22                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₁NO₃

Average Mass

357.4940 Da

Monoisotopic Mass

357.23039 Da

IUPAC Name

9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-4-one

Traditional Name

9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-4-one

CAS Registry Number

Not Available

SMILES

CC1CN2C3C1CCC31CCC(=O)OC1(C)C1CC(O)C3CCC=C3C21

InChI Identifier

InChI=1S/C22H31NO3/c1-12-11-23-19-15-5-3-4-14(15)17(24)10-16(19)21(2)22(9-7-18(25)26-21)8-6-13(12)20(22)23/h5,12-14,16-17,19-20,24H,3-4,6-11H2,1-2H3

InChI Key

YCFFNWSZGGOQEQ-UHFFFAOYSA-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
Daphniphyllum oldhamii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolidines

Sub Class

Not Available

Direct Parent

Quinolidines

Alternative Parents

Substituents

Quinolidine
Indolizidine
Delta valerolactone
Delta_valerolactone
Oxane
Piperidine
N-alkylpyrrolidine
Pyrrolidine
Cyclic alcohol
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Lactone
Oxacycle
Azacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Amine
Hydrocarbon derivative
Carbonyl group
Alcohol
Organic oxide
Organonitrogen compound
Organooxygen 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	2.12	ChemAxon
pKa (Strongest Acidic)	14.87	ChemAxon
pKa (Strongest Basic)	11.45	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.77 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	99.18 m³·mol⁻¹	ChemAxon
Polarizability	39.97 Å³	ChemAxon
Number of Rings	6	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

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

163106686

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one (NP0282125)

MOL for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D MOL for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D SDF for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D-SDF for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

PDB for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D PDB for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

SMILES for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

INCHI for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

Structure for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D Structure for NP0282125 (9-hydroxy-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)