NP-MRD: Showing NP-Card for 18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate (NP0265501)

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Record Information

Version

2.0

Created at

2022-09-08 09:30:23 UTC

Updated at

2022-09-08 09:30:23 UTC

NP-MRD ID

NP0265501

Secondary Accession Numbers

None

Natural Product Identification

Common Name

18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate

Description

Methyl 18-[(acetyloxy)methyl]-13-ethylidene-15-oxo-8,15λ⁵-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]Octadeca-2,4,6,8-tetraene-18-carboxylate belongs to the class of organic compounds known as corynanthean-type alkaloids. These are alkaloids with a structure based on the corynanthean nucleus, which is a tetracycle characterized by an indole fused to a quinolizidine. Additionally, the quinolizidine ring system is substituted to a 2-methylpropyl group and one ethyl group. 18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate is found in Kopsia griffithii. Based on a literature review very few articles have been published on methyl 18-[(acetyloxy)methyl]-13-ethylidene-15-oxo-8,15λ⁵-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]Octadeca-2,4,6,8-tetraene-18-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082211302D          

 30 34  0  0  0  0            999 V2000
   -1.9077    0.7429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4736    1.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6490    1.4193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1878    0.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7241    0.4340    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    0.6740   -0.3895    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    1.9433    0.6394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1539    1.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4617    1.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659    1.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6321    0.4487    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3778    0.8017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1391    0.4838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7950    0.9841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6897    1.8024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9284    2.1203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2724    1.6199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4887    1.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3712    2.0571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1624    2.1700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8276    2.4625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6424    3.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1464    3.5080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3317    4.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2720    4.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1205    4.5535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4000    3.0566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2007    2.8580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1716    3.8494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7440    4.4435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  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
  5  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  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  9 17  1  0  0  0  0
 10 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
  9 21  1  0  0  0  0
 21 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
 24 26  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  CHG  2   5   1   6  -1
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
    3.0281    2.6092   -0.6684 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6548    2.8231   -1.1545 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5552    2.4059   -0.5789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7371    2.7729   -1.2167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9170    2.2414   -0.6612 N   0  0  1  0  0  4  0  0  0  0  0  0
   -2.8988    3.1950   -0.8730 O   0  0  0  0  0  1  0  0  0  0  0  0
   -2.3934    1.0999   -1.4481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3655   -0.0330   -1.3525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9894   -0.3312    0.0676 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0001    0.3961    0.9154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6517   -0.4183    1.6129 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2444   -1.7522    1.3533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6710   -2.9932    1.8416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1202   -4.1743    1.3948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1231   -4.1600    0.4431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6952   -2.9252   -0.0458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2423   -1.7424    0.3996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9470    1.8992    0.7216 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6463    2.2607    1.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4895    1.6363    0.6717 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3284    0.1537    0.5388 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5155   -0.4630   -0.1949 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6186   -0.1704   -1.5291 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6352   -0.6926   -2.2764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7967   -0.4072   -3.7367 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4749   -1.4450   -1.7241 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5310   -0.4037    1.9295 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8568    0.3515    2.8557 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3689   -1.7492    2.2246 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5646   -2.2590    3.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6222    3.5573   -0.7469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0652    2.2700    0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5226    1.8730   -1.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5881    3.3967   -2.1020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537    3.8894   -1.2382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6857    2.4777   -2.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3112    0.7408   -0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4899    1.4307   -2.4784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9266   -0.9320   -1.7327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5740    0.1511   -2.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4561   -3.0204    2.5915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4795   -5.1244    1.8004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6942   -5.0796    0.0945 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0728   -2.9901   -0.8044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7775    2.3860    1.2670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7697    1.8373    2.4640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5236    3.3512    1.5213 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3961    1.8210    1.3045 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4090   -0.0208    0.3765 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5665   -1.5272    0.0538 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8005   -0.1307   -4.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5593    0.3710   -3.8860 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1819   -1.3284   -4.2327 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5481   -1.3998    4.2426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2340   -2.9743    3.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5676   -2.7509    3.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
 30 29  1  0
 29 27  1  0
 27 28  2  0
 21 27  1  1
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  2  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17  9  1  0
  9  8  1  6
  8  7  1  0
  7  5  1  0
  5  6  1  1
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  9 21  1  0
  3 20  1  0
  5 18  1  0
  9 10  1  0
 17 12  1  0
 30 54  1  0
 30 55  1  0
 30 56  1  0
 22 49  1  0
 22 50  1  0
 25 51  1  0
 25 52  1  0
 25 53  1  0
 20 48  1  1
 19 46  1  0
 19 47  1  0
 18 45  1  1
 13 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
  8 39  1  0
  8 40  1  0
  7 37  1  0
  7 38  1  0
  4 35  1  0
  4 36  1  0
  2 34  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
M  CHG  2   5   1   6  -1
M  END


  Mrv1652309082211302D          

 30 34  0  0  0  0            999 V2000
   -1.9077    0.7429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4736    1.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6490    1.4193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1878    0.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7241    0.4340    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    0.6740   -0.3895    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    1.9433    0.6394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1539    1.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4617    1.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659    1.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6321    0.4487    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3778    0.8017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1391    0.4838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7950    0.9841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6897    1.8024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9284    2.1203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2724    1.6199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4887    1.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3712    2.0571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1624    2.1700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8276    2.4625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6424    3.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1464    3.5080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3317    4.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2720    4.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1205    4.5535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4000    3.0566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2007    2.8580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1716    3.8494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7440    4.4435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  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
  5  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  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  9 17  1  0  0  0  0
 10 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
  9 21  1  0  0  0  0
 21 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
 24 26  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  CHG  2   5   1   6  -1
M  END
> <DATABASE_ID>
NP0265501

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1(COC(C)=O)C2CC3C4=NC5=CC=CC=C5C14CC[N+]3([O-])CC2=CC

> <INCHI_IDENTIFIER>
InChI=1S/C23H26N2O5/c1-4-15-12-25(28)10-9-22-16-7-5-6-8-18(16)24-20(22)19(25)11-17(15)23(22,21(27)29-3)13-30-14(2)26/h4-8,17,19H,9-13H2,1-3H3

> <INCHI_KEY>
NOAKEBKHIHDDFB-UHFFFAOYSA-N

> <FORMULA>
C23H26N2O5

> <MOLECULAR_WEIGHT>
410.47

> <EXACT_MASS>
410.184171945

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.93299507871848

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0^{1,9}.0^{2,7}.0^{10,15}]octadeca-2,4,6,8-tetraen-15-ium-15-olate

> <JCHEM_LOGP>
1.5296931953333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.528278393733454

> <JCHEM_POLAR_SURFACE_AREA>
88.02000000000001

> <JCHEM_REFRACTIVITY>
112.73659999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0^{1,9}.0^{2,7}.0^{10,15}]octadeca-2,4,6,8-tetraen-15-ium-15-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.561   1.387   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.751   2.696   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.211   2.649   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.351   1.125   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       1.352   0.810   0.000  0.00  0.00           N+1
HETATM    6  O   UNK     0       1.258  -0.727   0.000  0.00  0.00           O-1
HETATM    7  C   UNK     0       3.627   1.194   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.021   2.423   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.728   3.309   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.990   1.958   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       3.047   0.837   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       4.439   1.496   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.860   0.903   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.084   1.837   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.887   3.364   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.466   3.958   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.242   3.024   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.912   2.107   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.693   3.840   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.303   4.051   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.545   4.597   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.199   6.097   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.273   6.548   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.619   8.049   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.508   9.099   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.092   8.500   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.613   5.706   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.108   5.335   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.187   7.186   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.255   8.295   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   18                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   17   21                                             
CONECT   10    9   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12    9                                                  
CONECT   18   10    5   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19    3   21                                                  
CONECT   21   20    9   22   27                                             
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   21   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Value	Source
Methyl 18-[(acetyloxy)methyl]-13-ethylidene-15-oxo-8,15-diazapentacyclo[10.5.1.0,.0,.0,]octadeca-2,4,6,8-tetraene-18-carboxylic acid	Generator

Chemical Formula

C₂₃H₂₆N₂O₅

Average Mass

410.4700 Da

Monoisotopic Mass

410.18417 Da

IUPAC Name

18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0^{1,9}.0^{2,7}.0^{10,15}]octadeca-2,4,6,8-tetraen-15-ium-15-olate

Traditional Name

18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0^{1,9}.0^{2,7}.0^{10,15}]octadeca-2,4,6,8-tetraen-15-ium-15-olate

CAS Registry Number

Not Available

SMILES

COC(=O)C1(COC(C)=O)C2CC3C4=NC5=CC=CC=C5C14CC[N+]3([O-])CC2=CC

InChI Identifier

InChI=1S/C23H26N2O5/c1-4-15-12-25(28)10-9-22-16-7-5-6-8-18(16)24-20(22)19(25)11-17(15)23(22,21(27)29-3)13-30-14(2)26/h4-8,17,19H,9-13H2,1-3H3

InChI Key

NOAKEBKHIHDDFB-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
Kopsia griffithii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as corynanthean-type alkaloids. These are alkaloids with a structure based on the corynanthean nucleus, which is a tetracycle characterized by an indole fused to a quinolizidine. Additionally, the quinolizidine ring system is substituted to a 2-methylpropyl group and one ethyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Corynanthean-type alkaloids

Sub Class

Not Available

Direct Parent

Corynanthean-type alkaloids

Alternative Parents

Substituents

Corynanthean skeleton
Akuammilan skeleton
Quinolizidine
3-alkylindole
Indole or derivatives
Dicarboxylic acid or derivatives
Piperidine
Benzenoid
Methyl ester
Trialkyl amine oxide
Carboxylic acid ester
Ketimine
Organic 1,3-dipolar compound
Trisubstituted n-oxide
Propargyl-type 1,3-dipolar organic compound
N-oxide
Organoheterocyclic compound
Carboxylic acid derivative
Azacycle
Organic oxide
Organopnictogen compound
Imine
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organonitrogen compound
Carbonyl group
Organooxygen compound
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	1.53	ChemAxon
pKa (Strongest Basic)	3.53	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	88.02 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	112.74 m³·mol⁻¹	ChemAxon
Polarizability	42.93 Å³	ChemAxon
Number of Rings	5	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

73208441

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate (NP0265501)

MOL for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)

3D MOL for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)

3D SDF for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)

3D-SDF for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)

PDB for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)

3D PDB for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)

SMILES for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)

INCHI for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)

Structure for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)

3D Structure for NP0265501 (18-[(acetyloxy)methyl]-13-ethylidene-18-(methoxycarbonyl)-8,15-diazapentacyclo[10.5.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵]octadeca-2,4,6,8-tetraen-15-ium-15-olate)