NP-MRD: Showing NP-Card for 1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone (NP0243711)

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Record Information

Version

2.0

Created at

2022-09-07 04:19:18 UTC

Updated at

2022-09-07 04:19:19 UTC

NP-MRD ID

NP0243711

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone

Description

Crepidine belongs to the class of organic compounds known as phenylpiperidines. Phenylpiperidines are compounds containing a phenylpiperidine skeleton, which consists of a piperidine bound to a phenyl group. 1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone is found in Dendrobium crepidatum. Based on a literature review very few articles have been published on Crepidine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072206192D          

 25 28  0  0  1  0            999 V2000
    0.3565    1.4492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2702    0.6287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4835    0.2931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9377    0.1437    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6913    0.4793    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9463    1.2639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7713    1.2639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    0.4793    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7799    0.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661   -0.6767    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6198   -1.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987   -1.1617    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8056   -1.7205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7704   -1.8668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1668   -2.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7385   -3.2953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9137   -3.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5172   -2.5535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9456   -1.8484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725   -0.8261    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5189   -1.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -0.6767    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3435   -1.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0284   -0.6192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3588   -0.0056    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
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  4 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 20 25  1  6  0  0  0
  8 25  1  1  0  0  0
  5 25  1  6  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -4.8217   -0.6687   -0.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8419    0.4307   -0.2214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1157    1.5636   -0.6391 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5250    0.2572    0.4705 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7731   -0.9248   -0.0877 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9117   -2.1392    0.8501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285   -2.9739    0.3687 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3373   -1.8786    0.2565 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3297   -2.1981   -0.8664 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9956   -0.9992   -1.4234 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6745   -0.9205   -2.9117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6377    0.3269   -0.8028 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8806    1.2838   -1.8452 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5944    0.7269    0.2470 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9100    2.0441    0.5408 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8314    2.3565    1.5159 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4794    1.3835    2.2404 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1931    0.0791    1.9786 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2560   -0.2412    0.9858 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2013    0.4080   -0.5073 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2613    1.4047    0.5206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7652    1.5478    0.2879 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3487    2.6310    1.1687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8895    1.9664   -1.0338 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4085   -0.8027   -0.1682 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8268   -0.2074   -0.5008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8505   -1.4301    0.3475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6634   -1.1757   -1.4151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7242    0.0695    1.5381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2319   -1.2415   -1.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8477   -2.6697    0.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7268   -1.7830    1.8985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4305   -3.7579    1.0642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9271   -3.3052   -0.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8162   -1.8411    1.2453 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0163   -3.0033   -0.5380 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6898   -2.6990   -1.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1221   -1.0902   -1.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5991   -0.7176   -3.0221 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2304   -0.1066   -3.4234 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8643   -1.9146   -3.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2874    2.0695   -1.6064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4146    2.8297   -0.0236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0663    3.3857    1.7362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2135    1.6464    3.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6960   -0.7160    2.5404 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1047   -1.3176    0.8538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3128    0.7373   -1.4713 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1329    2.4261    0.3673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0649    1.0373    1.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9225    3.3911    0.5607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0178    2.2855    1.9465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5013    3.1558    1.6206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1356    1.2793   -1.6671 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  4 22  1  0
 22 23  1  0
 22 24  1  6
 22 21  1  0
 21 20  1  0
 20 25  1  0
 20 12  1  0
 12 13  1  6
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 12 10  1  0
 19 14  1  0
 25  8  1  0
 25  5  1  0
 11 39  1  0
 11 40  1  0
 11 41  1  0
 10 38  1  6
  9 36  1  0
  9 37  1  0
  8 35  1  1
  7 33  1  0
  7 34  1  0
  6 31  1  0
  6 32  1  0
  5 30  1  6
  4 29  1  1
  1 26  1  0
  1 27  1  0
  1 28  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  0
 21 49  1  0
 21 50  1  0
 20 48  1  6
 13 42  1  0
 15 43  1  0
 16 44  1  0
 17 45  1  0
 18 46  1  0
 19 47  1  0
M  END


  Mrv1652309072206192D          

 25 28  0  0  1  0            999 V2000
    0.3565    1.4492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2702    0.6287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4835    0.2931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9377    0.1437    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6913    0.4793    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9463    1.2639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7713    1.2639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    0.4793    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7799    0.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661   -0.6767    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6198   -1.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987   -1.1617    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8056   -1.7205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7704   -1.8668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1668   -2.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7385   -3.2953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9137   -3.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5172   -2.5535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9456   -1.8484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725   -0.8261    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5189   -1.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -0.6767    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3435   -1.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0284   -0.6192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3588   -0.0056    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
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  4 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 20 25  1  6  0  0  0
  8 25  1  1  0  0  0
  5 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0243711

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@H]2CC[C@H]3[C@H](C(C)=O)[C@](C)(O)C[C@H](N23)[C@@]1(O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H29NO3/c1-13-11-16-9-10-17-19(14(2)23)20(3,24)12-18(22(16)17)21(13,25)15-7-5-4-6-8-15/h4-8,13,16-19,24-25H,9-12H2,1-3H3/t13-,16+,17+,18+,19+,20-,21+/m1/s1

> <INCHI_KEY>
DCDDFWOASGCFGZ-JMMKEXGVSA-N

> <FORMULA>
C21H29NO3

> <MOLECULAR_WEIGHT>
343.467

> <EXACT_MASS>
343.214743798

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.48124009013871

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[(1S,4S,5S,6R,8S,9S,10R)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0^{4,12}]dodecan-5-yl]ethan-1-one

> <JCHEM_LOGP>
2.0995605473333327

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.527940774804918

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.323950086229424

> <JCHEM_PKA_STRONGEST_BASIC>
10.043647783504433

> <JCHEM_POLAR_SURFACE_AREA>
60.77

> <JCHEM_REFRACTIVITY>
96.9061

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-[(1S,4S,5S,6R,8S,9S,10R)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0^{4,12}]dodecan-5-yl]ethanone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       0.665   2.705   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.504   1.174   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.902   0.547   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       1.750   0.268   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.157   0.895   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.633   2.359   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.173   2.359   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.649   0.895   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.056   0.268   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.217  -1.263   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.624  -1.890   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.971  -2.168   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.104  -3.212   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.171  -3.485   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.911  -4.835   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.112  -6.151   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.572  -6.117   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.832  -4.766   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.632  -3.450   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.242  -1.542   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.835  -2.168   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.589  -1.263   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.641  -2.477   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.053  -1.156   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0       4.403  -0.010   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   22                                                  
CONECT    5    4    6   25                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   25                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14   20                                             
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20   12   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21    4   23   24                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20    8    5                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₉NO₃

Average Mass

343.4670 Da

Monoisotopic Mass

343.21474 Da

IUPAC Name

1-[(1S,4S,5S,6R,8S,9S,10R)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0^{4,12}]dodecan-5-yl]ethan-1-one

Traditional Name

1-[(1S,4S,5S,6R,8S,9S,10R)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0^{4,12}]dodecan-5-yl]ethanone

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@H]2CC[C@H]3[C@H](C(C)=O)[C@](C)(O)C[C@H](N23)[C@@]1(O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C21H29NO3/c1-13-11-16-9-10-17-19(14(2)23)20(3,24)12-18(22(16)17)21(13,25)15-7-5-4-6-8-15/h4-8,13,16-19,24-25H,9-12H2,1-3H3/t13-,16+,17+,18+,19+,20-,21+/m1/s1

InChI Key

DCDDFWOASGCFGZ-JMMKEXGVSA-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
Dendrobium crepidatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpiperidines. Phenylpiperidines are compounds containing a phenylpiperidine skeleton, which consists of a piperidine bound to a phenyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Piperidines

Sub Class

Phenylpiperidines

Direct Parent

Phenylpiperidines

Alternative Parents

Substituents

Phenylpiperidine
Quinolizidine
Indolizidine
Aralkylamine
Monocyclic benzene moiety
Beta-aminoketone
Benzenoid
N-alkylpyrrolidine
Pyrrolidine
Tertiary alcohol
1,2-aminoalcohol
Ketone
Tertiary amine
Tertiary aliphatic amine
Azacycle
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Amine
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	2.1	ChemAxon
pKa (Strongest Acidic)	13.32	ChemAxon
pKa (Strongest Basic)	10.04	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	60.77 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	96.91 m³·mol⁻¹	ChemAxon
Polarizability	38.48 Å³	ChemAxon
Number of Rings	4	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

58913423

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101306730

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone (NP0243711)

MOL for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)

3D MOL for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)

3D SDF for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)

3D-SDF for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)

PDB for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)

3D PDB for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)

SMILES for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)

INCHI for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)

Structure for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)

3D Structure for NP0243711 (1-[(1s,4s,5s,6r,8s,9s,10r)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.0⁴,¹²]dodecan-5-yl]ethanone)