NP-MRD: Showing NP-Card for 3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate (NP0316213)

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Record Information

Version

2.0

Created at

2022-09-11 15:14:59 UTC

Updated at

2022-09-11 15:14:59 UTC

NP-MRD ID

NP0316213

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate

Description

3,6,19-Trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]Nonadecan-10-yl acetate belongs to the class of organic compounds known as hetisine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hetisine skeleton, which is a heptacyclic compound with an additional N-C-6 bond as compared with the hetidine-type, and thus, is one of most complex entries in the atisane-class. 3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate is found in Consolida ajacis. Based on a literature review very few articles have been published on 3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]Nonadecan-10-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112217152D          

 28 34  0  0  0  0            999 V2000
   -1.1906    0.4800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3845    0.3045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2644    0.8553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1203    0.6350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9611    1.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7940    0.6205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4176   -0.0472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0434   -0.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4083   -1.4206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8224   -0.3315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3560    0.4002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8254    1.0787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4804    0.5843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5733    0.1461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0890   -0.6085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2832   -0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6437   -0.9351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6973   -1.7584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0110   -2.2164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0645   -3.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7287   -1.8511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0301   -0.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7342   -0.0353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7014    0.7890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6811    0.1655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8546   -0.3506    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3006   -1.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0853   -1.8780    0.0000 O   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  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 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
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  4 25  1  0  0  0  0
 14 25  1  0  0  0  0
 15 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 57 63  0  0  0  0  0  0  0  0999 V2000
   -3.9342   -2.5932   -1.3318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8292   -2.0153   -0.9394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6876   -2.7707   -0.3489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6188   -1.7875   -0.0147 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5578   -2.4054    0.6610 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6051   -1.4012    1.0051 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9921   -0.5726   -0.2329 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6811    0.0835   -0.5346 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7692    1.3655   -1.2734 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8699    2.2484   -0.8182 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1804    3.1294   -1.8670 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1206    1.5751   -0.3985 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9411    0.3851    0.4726 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2585   -0.3159    0.6767 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2092    0.6455    1.7479 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0500    0.3063    2.8070 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0615   -0.2763    1.7858 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0759    0.2637    0.8483 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1177   -0.6727    0.9130 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3707   -0.0520    0.3794 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3759    1.3464    0.4826 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3037    2.0604    1.2159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3079    3.5411    1.3241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1940    1.4104    1.8248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6163   -0.5254   -1.0523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3771   -0.3645   -1.9090 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6087   -1.1493   -3.0634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1974   -0.9391   -1.2151 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0281   -3.6662   -1.2252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7560   -2.0395   -1.7583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0466   -3.2103    0.6028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2736   -3.5149   -1.0313 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9958   -3.1574    0.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1883   -2.8360    1.6310 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4727   -1.8477    1.4877 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4365   -1.1553   -1.0170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8572    1.1323   -2.3637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1946    1.9268   -1.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5162    2.8838    0.0376 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1458    3.1623   -2.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7543    2.3195    0.1379 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7266    1.2600   -1.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0591    0.4361    0.6767 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3055   -0.8310    1.6717 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3660   -1.0651   -0.1353 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8786    1.6951    1.8603 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7849   -0.5059    3.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1912    1.2984    1.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2268   -1.1143    1.9082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2208   -0.5040    0.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2578    3.9525    1.2775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6717    3.7890    2.3443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9521    4.0088    0.5414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5149   -0.0952   -1.4861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2843    0.6615   -2.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1431   -1.9992   -3.0375 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4407   -1.5038   -1.9141 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 24  2  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17  6  1  0
  6  5  1  0
  4  5  1  1
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28  8  1  0
  8  9  1  6
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 13  7  1  0
 25 20  1  0
  7  8  1  0
  4 19  1  0
 28  4  1  0
  8 18  1  0
 15 17  1  0
  7  6  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 20 50  1  1
 19 49  1  1
 18 48  1  1
  6 35  1  1
  5 33  1  0
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  3 31  1  0
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  1 29  1  0
  1 30  1  0
 25 54  1  6
 26 55  1  6
 27 56  1  0
 28 57  1  6
  9 37  1  0
  9 38  1  0
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 11 40  1  0
 12 41  1  0
 12 42  1  0
 14 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  1
 16 47  1  0
  7 36  1  6
M  END


  Mrv1652309112217152D          

 28 34  0  0  0  0            999 V2000
   -1.1906    0.4800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3845    0.3045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2644    0.8553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1203    0.6350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9611    1.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7940    0.6205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4176   -0.0472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0434   -0.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4083   -1.4206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8224   -0.3315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3560    0.4002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8254    1.0787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4804    0.5843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5733    0.1461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0890   -0.6085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2832   -0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6437   -0.9351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6973   -1.7584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0110   -2.2164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0645   -3.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7287   -1.8511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0301   -0.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7342   -0.0353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7014    0.7890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6811    0.1655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8546   -0.3506    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3006   -1.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0853   -1.8780    0.0000 O   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  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 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
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  4 25  1  0  0  0  0
 14 25  1  0  0  0  0
 15 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0316213

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1C2C3N4C5CC22CC(=C)C1C(O)C2C31CC(O)CC(C)(C4O)C51

> <INCHI_IDENTIFIER>
InChI=1S/C22H29NO5/c1-8-4-21-7-11-16-20(3)5-10(25)6-22(16)17(21)14(26)12(8)15(28-9(2)24)13(21)18(22)23(11)19(20)27/h10-19,25-27H,1,4-7H2,2-3H3

> <INCHI_KEY>
JFDDBMVESRQDLZ-UHFFFAOYSA-N

> <FORMULA>
C22H29NO5

> <MOLECULAR_WEIGHT>
387.476

> <EXACT_MASS>
387.204573038

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
40.934981734364676

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{7,16}.0^{9,14}.0^{14,18}]nonadecan-10-yl acetate

> <JCHEM_LOGP>
-0.8458631233333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.447101499763392

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.101566579132335

> <JCHEM_PKA_STRONGEST_BASIC>
7.702399765716385

> <JCHEM_POLAR_SURFACE_AREA>
90.23

> <JCHEM_REFRACTIVITY>
98.64

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{7,16}.0^{9,14}.0^{14,18}]nonadecan-10-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.223   0.896   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.718   0.568   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.494   1.597   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.091   1.185   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.661   1.913   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.216   1.158   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.379  -0.088   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.548  -1.271   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.229  -2.652   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.002  -0.619   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.131   0.747   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.007   2.014   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.497   1.091   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.803   0.273   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.900  -1.136   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.395  -0.629   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.202  -1.746   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.302  -3.282   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.021  -4.137   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.120  -5.674   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.360  -3.455   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.056  -0.843   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.370  -0.066   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.309   1.473   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.138   0.309   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       5.329  -0.655   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       6.161  -2.019   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.759  -3.506   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   16   25                                             
CONECT    5    4    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8   14                                                  
CONECT    8    7    9   10   27                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    7   15   25                                             
CONECT   15   14   16   26                                                  
CONECT   16   15    4   17                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17    2   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    4   14                                                  
CONECT   26   15    6   27                                                  
CONECT   27   26    8   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   68    0
END

View in JSmol

Synonyms

Value	Source
3,6,19-Trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0,.0,.0,.0,.0,]nonadecan-10-yl acetic acid	Generator

Chemical Formula

C₂₂H₂₉NO₅

Average Mass

387.4760 Da

Monoisotopic Mass

387.20457 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OC1C2C3N4C5CC22CC(=C)C1C(O)C2C31CC(O)CC(C)(C4O)C51

InChI Identifier

InChI=1S/C22H29NO5/c1-8-4-21-7-11-16-20(3)5-10(25)6-22(16)17(21)14(26)12(8)15(28-9(2)24)13(21)18(22)23(11)19(20)27/h10-19,25-27H,1,4-7H2,2-3H3

InChI Key

JFDDBMVESRQDLZ-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
Consolida ajacis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hetisine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hetisine skeleton, which is a heptacyclic compound with an additional N-C-6 bond as compared with the hetidine-type, and thus, is one of most complex entries in the atisane-class.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Hetisine-type diterpenoid alkaloids

Alternative Parents

Substituents

Hetisine-type diterpenoid alkaloid
Azaspirodecane
Quinolizidine
Indole or derivatives
Alkaloid or derivatives
Indolizidine
Isoindoline
Isoindole or derivatives
Azepane
N-alkylpyrrolidine
Piperidine
Cyclic alcohol
Pyrrolidine
Carboxylic acid ester
Hemiaminal
Secondary alcohol
Alkanolamine
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Alcohol
Organic nitrogen compound
Organic oxygen compound
Organooxygen compound
Carbonyl group
Organonitrogen 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

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

163104543

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate (NP0316213)

MOL for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)

3D MOL for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)

3D SDF for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)

3D-SDF for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)

PDB for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)

3D PDB for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)

SMILES for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)

INCHI for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)

Structure for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)

3D Structure for NP0316213 (3,6,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]nonadecan-10-yl acetate)