NP-MRD: Showing NP-Card for 5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione (NP0240709)

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Record Information

Version

2.0

Created at

2022-09-07 00:35:55 UTC

Updated at

2022-09-07 00:35:55 UTC

NP-MRD ID

NP0240709

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione

Description

AC1NAS4G belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12. 5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione is found in Thalictrum javanicum. AC1NAS4G is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171521062D          

 26 32  0  0  0  0            999 V2000
    2.9370    4.0236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3881    3.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0858    2.8666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8247    2.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073    2.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2151    2.5350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3233    1.7652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4562    1.6886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9835    1.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2030    1.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3386    1.8317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1569    1.7271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0378    2.5926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913    2.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0549    3.5121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8681    3.8136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0001    4.6280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5298    3.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3197    2.3598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3695    2.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2429    2.6275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2327    1.6647    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8597    1.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5634    1.5592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3713    2.3615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5489    2.4267    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  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  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
  2 18  1  0  0  0  0
  6 18  1  0  0  0  0
 14 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  2  0  0  0  0
  7 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
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
 22 26  1  0  0  0  0
M  END

     RDKit          3D

 53 59  0  0  0  0  0  0  0  0999 V2000
    5.1699   -0.5421    0.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8873   -0.2374    0.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2599    0.0732   -1.1323 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7884    0.0923   -0.9819 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0015    0.3230   -2.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2929    1.0162   -2.0742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8697    1.3046   -3.1092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9601    1.3959   -0.8071 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2684    0.7668   -0.5157 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1452    0.9225   -1.7660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8644    1.6894    0.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7588    2.0161    1.5308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6503    0.9772    1.5508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0392    0.7365    0.2325 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3527    1.1865    0.0216 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2249    1.0928    1.2196 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3162    1.9985    2.0070 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9683   -0.1830    1.3758 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9168   -1.2747    1.1372 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2689   -1.1287   -0.1754 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1335   -0.7316   -0.2186 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1802   -1.2420    0.5084 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4346   -2.6665    0.3900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8373   -2.6806   -0.1940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7816   -1.5171   -0.9978 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3792   -0.5878   -0.0221 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8256   -0.5812   -0.5595 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5309   -0.7549    1.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5898    1.1098   -1.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5483   -0.6577   -1.8833 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6335    0.9865   -2.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9064   -0.6191   -2.8281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9189    2.4667   -0.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1826    0.6975   -1.4565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0074    1.8893   -2.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8317    0.0664   -2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7550    1.2581    1.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1017    2.6366    0.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2973    2.9933    1.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2170    1.9860    2.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0713    0.0284    1.9940 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0986    1.3274    2.2700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4692    2.1333   -0.5214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4891   -0.2968    2.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4663   -2.2372    1.1973 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1644   -1.2865    1.9394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4578   -1.9974   -0.8423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4230   -0.8411   -1.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4918   -3.1579    1.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7088   -3.1669   -0.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5262   -2.5030    0.6635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0597   -3.5770   -0.7707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1467   -0.7031    0.8006 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  1  6
  9 11  1  0
 11 12  1  0
 12 13  1  0
 14 13  1  1
 14 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  6
  5  6  1  0
  6  7  2  0
  6  8  1  0
  4 15  1  0
 15 16  1  0
 16 17  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
  8  9  1  0
 26 22  1  0
 26  9  1  0
  8 14  1  0
 15 14  1  0
  4 20  1  0
 16 18  1  0
 10 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 21 48  1  6
 20 47  1  6
 19 45  1  0
 19 46  1  0
 18 44  1  1
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  0
  5 32  1  0
  8 33  1  1
 15 43  1  6
 23 49  1  0
 23 50  1  0
 24 51  1  0
 24 52  1  0
 26 53  1  1
M  END


  Mrv1533004171521062D          

 26 32  0  0  0  0            999 V2000
    2.9370    4.0236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3881    3.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0858    2.8666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8247    2.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073    2.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2151    2.5350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3233    1.7652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4562    1.6886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9835    1.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2030    1.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3386    1.8317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1569    1.7271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0378    2.5926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913    2.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0549    3.5121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8681    3.8136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0001    4.6280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5298    3.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3197    2.3598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3695    2.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2429    2.6275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2327    1.6647    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8597    1.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5634    1.5592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3713    2.3615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5489    2.4267    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  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  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
  2 18  1  0  0  0  0
  6 18  1  0  0  0  0
 14 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  2  0  0  0  0
  7 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
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
 22 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240709

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CCCC34C(C5CC6C(=C)CC5(CC(=O)C13)C4C6=O)N1CCOC21

> <INCHI_IDENTIFIER>
InChI=1S/C22H27NO3/c1-11-9-21-10-14(24)16-20(2)4-3-5-22(16)17(21)15(25)12(11)8-13(21)18(22)23-6-7-26-19(20)23/h12-13,16-19H,1,3-10H2,2H3

> <INCHI_KEY>
SMCYLHSXVDDYCA-UHFFFAOYSA-N

> <FORMULA>
C22H27NO3

> <MOLECULAR_WEIGHT>
353.462

> <EXACT_MASS>
353.199093733

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
38.20857692111365

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione

> <ALOGPS_LOGP>
1.45

> <JCHEM_LOGP>
2.3054015173333338

> <ALOGPS_LOGS>
-2.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
18.586011329469684

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.57525678853956

> <JCHEM_PKA_STRONGEST_BASIC>
6.968106137953905

> <JCHEM_POLAR_SURFACE_AREA>
46.61

> <JCHEM_REFRACTIVITY>
95.64309999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.68e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       5.482   7.511   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.325   6.221   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.627   5.351   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.140   3.796   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.427   3.839   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.135   4.732   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.337   3.295   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.718   3.152   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.836   1.913   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.379   2.252   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.632   3.419   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.160   3.224   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.071   4.840   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.664   4.899   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.969   6.556   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.487   7.119   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.734   8.639   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.722   6.127   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.463   4.405   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.690   3.873   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.453   4.905   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0       6.034   3.108   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       7.205   2.107   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.518   2.910   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.160   4.408   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.625   4.530   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   18   26                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   18   19                                             
CONECT    7    6    8   22                                                  
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   20                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    8   15   19                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    2    6                                                  
CONECT   19   14    6   20                                                  
CONECT   20   19   10   21                                                  
CONECT   21   20                                                            
CONECT   22    7   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    2   22                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₇NO₃

Average Mass

353.4620 Da

Monoisotopic Mass

353.19909 Da

IUPAC Name

5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione

Traditional Name

5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione

CAS Registry Number

Not Available

SMILES

CC12CCCC34C(C5CC6C(=C)CC5(CC(=O)C13)C4C6=O)N1CCOC21

InChI Identifier

InChI=1S/C22H27NO3/c1-11-9-21-10-14(24)16-20(2)4-3-5-22(16)17(21)15(25)12(11)8-13(21)18(22)23-6-7-26-19(20)23/h12-13,16-19H,1,3-10H2,2H3

InChI Key

SMCYLHSXVDDYCA-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
Thalictrum javanicum Blume	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Atisane diterpenoids

Alternative Parents

Substituents

Atisane diterpenoid
Alkaloid or derivatives
Piperidine
Oxazolidine
Hemiaminal
Ketone
Organoheterocyclic compound
Azacycle
Oxacycle
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Amine
Carbonyl group
Organic nitrogen 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	1.45	ALOGPS
logP	2.31	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	16.58	ChemAxon
pKa (Strongest Basic)	6.97	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	46.61 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	95.64 m³·mol⁻¹	ChemAxon
Polarizability	38.21 Å³	ChemAxon
Number of Rings	7	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

4481794

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione (NP0240709)

MOL for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)

3D MOL for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)

3D SDF for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)

3D-SDF for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)

PDB for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)

3D PDB for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)

SMILES for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)

INCHI for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)

Structure for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)

3D Structure for NP0240709 (5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁶,¹⁰.0¹²,¹⁷.0¹⁷,²¹]docosane-19,22-dione)