NP-MRD: Showing NP-Card for (1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane (NP0304221)

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Record Information

Version

2.0

Created at

2022-09-10 19:09:41 UTC

Updated at

2022-09-10 19:09:42 UTC

NP-MRD ID

NP0304221

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane

Description

Concavine belongs to the class of organic compounds known as monoterpenoids. Monoterpenoids are compounds containing a chain of two isoprene units. (1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane was first documented in 2017 (PMID: 28507709). Based on a literature review very few articles have been published on Concavine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102221092D          

 24 27  0  0  1  0            999 V2000
   -0.9683    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1557    0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1420    1.3144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6181    2.0338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4595    1.7955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5333    0.8991    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8433    1.0629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3763    0.7990    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8707    1.4594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6953    1.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4871    2.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4273    1.8652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2291    0.8557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0703    0.0462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3383   -0.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5844    0.0007    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8909   -0.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2392    0.0613    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3955   -0.1478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1411   -0.9326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6936   -1.5454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4391   -2.3302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9916   -2.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3677   -2.5022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  1  6  0  0  0
  3  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  8 16  1  6  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
    3.3050    0.3855   -1.8864 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0916    0.5229   -1.4051 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9696    0.8472   -2.3723 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4359   -0.4109   -3.0248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547   -0.9411   -2.0836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6191    0.0215   -0.8998 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2467    1.3028   -1.5723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8663    0.0432   -0.1217 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6356    1.3343   -0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8765    1.3275    0.6564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0525    0.9119   -0.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1280    2.8231    0.9643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7290    0.7393    1.8629 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7316   -0.6017    1.9936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3375   -1.1836    1.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5380   -0.1885    1.2407 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1390   -0.3350    1.4001 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4564   -0.4912    0.0216 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7064    0.3995   -0.0154 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6819   -0.1157    0.9678 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1732   -1.4668    0.8067 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4334   -1.8353    0.7876 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7989   -3.3037    0.6048 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5760   -0.9048    0.9673 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4896    0.4990   -2.9573 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1715    0.1645   -1.2944 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2804    1.6155   -3.1014 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2002   -1.1633   -3.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0912   -0.0818   -3.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6336   -0.9885   -2.5587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3155   -1.9445   -1.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0339    1.5230   -2.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0392    2.1421   -0.9132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5311   -0.7779   -0.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0050    2.2174    0.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9703    1.4574   -1.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4120   -0.1035   -0.0380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8340    1.0228   -1.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9529    1.5801   -0.0172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9649    2.8757    1.7165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2523    3.2692    1.4735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3997    3.3659    0.0515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0467   -0.8180    3.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4716   -1.1709    1.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8988   -1.4237    2.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3389   -2.1324    1.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1732   -1.1850    2.0110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2457    0.5820    1.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7415   -1.5285   -0.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3918    1.4221    0.3499 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1712   -0.0676    1.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5259    0.6262    1.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4131   -2.2615    0.6906 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9255   -3.8715    0.9478 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0905   -3.5008   -0.4357 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6205   -3.5058    1.3353 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052   -0.0790    1.6552 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9783   -0.5375    0.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3933   -1.4747    1.4903 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 24  1  0
 22 21  2  3
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 10  1  0
 10 11  1  0
 10 12  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  5  1  6
  5  4  1  0
  4  3  1  0
  3  7  1  0
  3  2  1  0
  2  1  2  3
  2 19  1  0
  6 18  1  0
  7  6  1  0
  8 16  1  0
 23 54  1  0
 23 55  1  0
 23 56  1  0
 24 57  1  0
 24 58  1  0
 24 59  1  0
 21 53  1  0
 20 51  1  0
 20 52  1  0
 19 50  1  1
 18 49  1  6
 17 47  1  0
 17 48  1  0
 15 45  1  0
 15 46  1  0
 14 43  1  0
 14 44  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 12 42  1  0
  9 35  1  0
  9 36  1  0
  8 34  1  6
  5 30  1  0
  5 31  1  0
  4 28  1  0
  4 29  1  0
  3 27  1  6
  7 32  1  0
  7 33  1  0
  1 25  1  0
  1 26  1  0
M  END


  Mrv1652309102221092D          

 24 27  0  0  1  0            999 V2000
   -0.9683    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1557    0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1420    1.3144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6181    2.0338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4595    1.7955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5333    0.8991    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8433    1.0629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3763    0.7990    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8707    1.4594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6953    1.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4871    2.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4273    1.8652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2291    0.8557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0703    0.0462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3383   -0.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5844    0.0007    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8909   -0.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2392    0.0613    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3955   -0.1478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1411   -0.9326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6936   -1.5454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4391   -2.3302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9916   -2.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3677   -2.5022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  1  6  0  0  0
  3  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  8 16  1  6  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0304221

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC[C@@H]1[C@H]2CN3CCOC(C)(C)C[C@H]3[C@]22CC[C@@H](C2)C1=C

> <INCHI_IDENTIFIER>
InChI=1S/C22H35NO/c1-15(2)6-7-18-16(3)17-8-9-22(12-17)19(18)14-23-10-11-24-21(4,5)13-20(22)23/h6,17-20H,3,7-14H2,1-2,4-5H3/t17-,18-,19+,20-,22-/m0/s1

> <INCHI_KEY>
SZGQNXGUSQDIFW-OTVISBKVSA-N

> <FORMULA>
C22H35NO

> <MOLECULAR_WEIGHT>
329.528

> <EXACT_MASS>
329.271864751

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
40.5645457830274

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,10R,11R,13S)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0^{1,10}.0^{2,8}]hexadecane

> <JCHEM_LOGP>
3.9925340979999993

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
11.421840216929798

> <JCHEM_POLAR_SURFACE_AREA>
12.47

> <JCHEM_REFRACTIVITY>
101.75999999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,10R,11R,13S)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0^{1,10}.0^{2,8}]hexadecane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.807   0.677   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.291   0.944   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.265   2.453   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.154   3.796   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.724   3.352   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.862   1.678   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.574   1.984   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.436   1.491   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.359   2.724   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.898   2.771   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.509   4.262   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.264   3.482   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.894   1.597   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.598   0.086   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.231  -0.624   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       4.824   0.001   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       3.530  -0.854   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.313   0.114   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.738  -0.276   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.263  -1.741   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.295  -2.885   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.820  -4.350   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.851  -5.493   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.686  -4.671   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   18                                             
CONECT    7    6    3                                                       
CONECT    8    6    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    8   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17    6   19                                                  
CONECT   19   18    2   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₅NO

Average Mass

329.5280 Da

Monoisotopic Mass

329.27186 Da

IUPAC Name

(1S,2S,10R,11R,13S)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0^{1,10}.0^{2,8}]hexadecane

Traditional Name

(1S,2S,10R,11R,13S)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0^{1,10}.0^{2,8}]hexadecane

CAS Registry Number

Not Available

SMILES

CC(C)=CC[C@@H]1[C@H]2CN3CCOC(C)(C)C[C@H]3[C@]22CC[C@@H](C2)C1=C

InChI Identifier

InChI=1S/C22H35NO/c1-15(2)6-7-18-16(3)17-8-9-22(12-17)19(18)14-23-10-11-24-21(4,5)13-20(22)23/h6,17-20H,3,7-14H2,1-2,4-5H3/t17-,18-,19+,20-,22-/m0/s1

InChI Key

SZGQNXGUSQDIFW-OTVISBKVSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monoterpenoids. Monoterpenoids are compounds containing a chain of two isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Monoterpenoids

Alternative Parents

Substituents

Monoterpenoid
Isoindoline
Isoindole or derivatives
Para-oxazepine
N-alkylpyrrolidine
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Azacycle
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Amine
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	3.99	ChemAxon
pKa (Strongest Basic)	11.42	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	12.47 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	101.76 m³·mol⁻¹	ChemAxon
Polarizability	40.56 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

78437370

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585709

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Saint-Dizier F, Simpkins NS: First total synthesis of concavine. Chem Sci. 2017 May 1;8(5):3384-3389. doi: 10.1039/c6sc05627j. Epub 2017 Feb 24. [PubMed:28507709 ]
LOTUS database [Link]

Showing NP-Card for (1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane (NP0304221)

MOL for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)

3D MOL for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)

3D SDF for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)

3D-SDF for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)

PDB for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)

3D PDB for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)

SMILES for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)

INCHI for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)

Structure for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)

3D Structure for NP0304221 ((1s,2s,10r,11r,13s)-4,4-dimethyl-11-(3-methylbut-2-en-1-yl)-12-methylidene-5-oxa-8-azatetracyclo[11.2.1.0¹,¹⁰.0²,⁸]hexadecane)