NP-MRD: Showing NP-Card for 19(S)-Hydroxyconopharyngine (NP0137801)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-05-31 16:34:13 UTC

Updated at

2022-05-31 16:34:13 UTC

NP-MRD ID

NP0137801

Secondary Accession Numbers

NP0078184

Natural Product Identification

Common Name

19(S)-Hydroxyconopharyngine

Description

19(S)-Hydroxyconopharyngine belongs to the class of organic compounds known as ibogan-type alkaloids. These are indole alkaloids with a structure based on the ibogamine skeleton or a derivative thereof. Ibogamine is a pentacyclic heterocyclic compound consisting of an indole fused to an azepane-containing tricyclic moiety ring. Iboga alkaloids arise from the cyclization of a secodine-type precursor through the formation of a 16,21 bond. Based on a literature review very few articles have been published on 19(S)-Hydroxyconopharyngine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201182D          

 30 34  0  0  1  0            999 V2000
    1.4186   -2.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1734   -1.9332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4050   -1.1015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9808   -0.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0359   -0.2350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4310   -1.1245    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7271   -1.8624    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4613   -1.4761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3956   -0.3913    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7214   -0.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668   -0.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1864   -0.6917    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0057   -0.7890    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4996   -0.1282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3310   -1.5471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7120    0.5237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2071    1.1836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1070    0.6226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    1.3813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5227    0.2282    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818   -0.0950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2090   -0.9168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8843   -1.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6324   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052   -0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0299    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4533    0.1268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5260    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3077   -1.5168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0557   -1.1689    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  1  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  5 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 13 15  1  1  0  0  0
  5 16  1  1  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
  4 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 21 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 60 64  0  0  0  0  0  0  0  0999 V2000
   -2.5446    3.8154    0.8871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8099    2.6450    1.0696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1566    1.4225    0.4477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1655    1.4260   -0.2873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2775    0.2924    0.7510 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1748    0.2631    2.2892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9587   -0.9527    2.7421 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3134   -1.0160    2.0992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2273   -1.2925    0.6118 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4673   -2.7823    0.3388 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3812   -3.0387   -1.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6958   -3.2030    0.8149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7626   -1.0358    0.2657 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0335   -2.1124    0.8928 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1771   -2.4702    0.2902 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3701   -1.6464    0.5753 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1645   -0.2406    0.0636 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0605    0.5717    0.1359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3847    1.7357   -0.4790 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6442    1.7025   -0.9391 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4394    2.6266   -1.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7349    2.3207   -1.9885 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5533    3.2283   -2.6811 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0525    4.5148   -3.0369 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2071    1.0739   -1.6387 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5107    0.7547   -1.9948 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0405   -0.5111   -1.6588 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4268    0.1613   -0.9585 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1367    0.4710   -0.6035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0924   -2.1475    2.3073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0840    4.1168    1.8322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2263    3.7947    0.0288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8085    4.6453    0.7064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5454    1.1763    2.7541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1006    0.0639    2.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0991   -0.9482    3.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9665   -1.7223    2.6207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7723   -0.0048    2.2010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -0.6783    0.0378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6898   -3.4288    0.7715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0731   -2.3411   -1.6490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6956   -4.0983   -1.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3258   -2.9199   -1.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3740   -2.4651    0.6867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6441   -1.1037   -0.8155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4144   -3.5324    0.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0259   -2.4754   -0.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3159   -2.0628    0.1662 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5360   -1.5771    1.6646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2511    2.5568   -0.5914 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0235    3.5776   -1.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8361    5.1791   -3.3996 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4680    4.9758   -2.2136 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3364    4.3357   -3.8746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4631   -1.3015   -2.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9943   -0.6754   -0.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1095   -0.4963   -1.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7897   -0.8266   -0.6771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4754   -3.0896    2.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0946   -1.9305    2.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  5  3  1  1
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
  9 13  1  0
 13 14  1  0
 14 30  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  2  0
 25 26  1  0
 26 27  1  0
 25 28  1  0
 28 29  2  0
 13  5  1  0
 29 17  1  0
 18  5  1  0
 29 20  1  0
 30  7  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  1
  8 37  1  0
  8 38  1  0
  9 39  1  6
 10 40  1  1
 11 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  6
 30 59  1  0
 30 60  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 19 50  1  0
 21 51  1  0
 24 52  1  0
 24 53  1  0
 24 54  1  0
 27 55  1  0
 27 56  1  0
 27 57  1  0
 28 58  1  0
M  END


  Mrv1652304292201182D          

 30 34  0  0  1  0            999 V2000
    1.4186   -2.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1734   -1.9332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4050   -1.1015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9808   -0.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0359   -0.2350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4310   -1.1245    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7271   -1.8624    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4613   -1.4761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3956   -0.3913    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7214   -0.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668   -0.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1864   -0.6917    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0057   -0.7890    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4996   -0.1282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3310   -1.5471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7120    0.5237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2071    1.1836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1070    0.6226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    1.3813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5227    0.2282    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818   -0.0950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2090   -0.9168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8843   -1.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6324   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052   -0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0299    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4533    0.1268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5260    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3077   -1.5168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0557   -1.1689    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  1  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  5 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 13 15  1  1  0  0  0
  5 16  1  1  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
  4 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 21 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0137801

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]12C[C@H]3C[C@H]([C@H](C)O)[C@@H]1N(C3)CCC1=C2NC2=CC(OC)=C(OC)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C23H30N2O5/c1-12(26)15-7-13-10-23(22(27)30-4)20-14(5-6-25(11-13)21(15)23)16-8-18(28-2)19(29-3)9-17(16)24-20/h8-9,12-13,15,21,24,26H,5-7,10-11H2,1-4H3/t12-,13+,15+,21-,23+/m0/s1

> <INCHI_KEY>
RCDVEJINCXVEQG-UNJQAPKOSA-N

> <FORMULA>
C23H30N2O5

> <MOLECULAR_WEIGHT>
414.502

> <EXACT_MASS>
414.215472074

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
45.467526036929556

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

> <ALOGPS_LOGP>
2.66

> <JCHEM_LOGP>
1.7804106326666664

> <ALOGPS_LOGS>
-3.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
16.631421448398445

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.200651023223813

> <JCHEM_PKA_STRONGEST_BASIC>
8.029477237725498

> <JCHEM_POLAR_SURFACE_AREA>
84.02000000000001

> <JCHEM_REFRACTIVITY>
112.51259999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.13e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       2.648  -4.307   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.057  -3.609   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.489  -2.056   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.698  -0.735   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.934  -0.439   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.805  -2.099   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       1.357  -3.476   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       2.728  -2.755   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.605  -0.730   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.213  -1.692   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.685  -0.121   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.348  -1.291   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.877  -1.473   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.799  -0.239   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.485  -2.888   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.329   0.978   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.253   2.209   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -0.200   1.162   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.804   2.578   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       4.709   0.426   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       6.126  -0.177   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.990  -1.711   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.251  -2.596   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.647  -1.947   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.783  -0.413   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.522   0.472   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.179   0.237   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      10.315   1.771   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       9.908  -2.831   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      11.304  -2.182   0.000  0.00  0.00           C+0
CONECT    1    2    7                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5   20                                                  
CONECT    5    4    6   10   16                                             
CONECT    6    5    7   12                                                  
CONECT    7    6    1    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9    5                                                       
CONECT   11    9   12                                                       
CONECT   12   11    6   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    5   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18                                                            
CONECT   20    4   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21    3   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   21                                                       
CONECT   27   25   28                                                       
CONECT   28   27                                                            
CONECT   29   24   30                                                       
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₀N₂O₅

Average Mass

414.5020 Da

Monoisotopic Mass

414.21547 Da

IUPAC Name

methyl (1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

Traditional Name

methyl (1S,15R,17S,18S)-17-[(1S)-1-hydroxyethyl]-6,7-dimethoxy-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

CAS Registry Number

16790-93-5

SMILES

COC(=O)[C@@]12C[C@H]3C[C@H]([C@H](C)O)[C@@H]1N(C3)CCC1=C2NC2=CC(OC)=C(OC)C=C12

InChI Identifier

InChI=1S/C23H30N2O5/c1-12(26)15-7-13-10-23(22(27)30-4)20-14(5-6-25(11-13)21(15)23)16-8-18(28-2)19(29-3)9-17(16)24-20/h8-9,12-13,15,21,24,26H,5-7,10-11H2,1-4H3/t12-,13+,15+,21-,23+/m0/s1

InChI Key

RCDVEJINCXVEQG-UNJQAPKOSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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 ibogan-type alkaloids. These are indole alkaloids with a structure based on the ibogamine skeleton or a derivative thereof. Ibogamine is a pentacyclic heterocyclic compound consisting of an indole fused to an azepane-containing tricyclic moiety ring. Iboga alkaloids arise from the cyclization of a secodine-type precursor through the formation of a 16,21 bond.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Ibogan-type alkaloids

Sub Class

Not Available

Direct Parent

Ibogan-type alkaloids

Alternative Parents

Substituents

Ibogan skeleton
Catharanthine skeleton
Pyrroloazepine
3-alkylindole
Indole
Indole or derivatives
Piperidinecarboxylic acid
Anisole
Phenol ether
Aralkylamine
Alkyl aryl ether
Azepine
Benzenoid
Piperidine
Pyrrole
Heteroaromatic compound
Methyl ester
1,3-aminoalcohol
Tertiary amine
Secondary alcohol
Amino acid or derivatives
Tertiary aliphatic amine
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Ether
Alcohol
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Amine
Organonitrogen compound
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	2.66	ALOGPS
logP	1.78	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	15.2	ChemAxon
pKa (Strongest Basic)	8.03	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	84.02 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	112.51 m³·mol⁻¹	ChemAxon
Polarizability	45.47 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

34965563

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102004638

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 19(S)-Hydroxyconopharyngine (NP0137801)

MOL for NP0137801 (19(S)-Hydroxyconopharyngine)

3D MOL for NP0137801 (19(S)-Hydroxyconopharyngine)

3D SDF for NP0137801 (19(S)-Hydroxyconopharyngine)

3D-SDF for NP0137801 (19(S)-Hydroxyconopharyngine)

PDB for NP0137801 (19(S)-Hydroxyconopharyngine)

3D PDB for NP0137801 (19(S)-Hydroxyconopharyngine)

SMILES for NP0137801 (19(S)-Hydroxyconopharyngine)

INCHI for NP0137801 (19(S)-Hydroxyconopharyngine)

Structure for NP0137801 (19(S)-Hydroxyconopharyngine)

3D Structure for NP0137801 (19(S)-Hydroxyconopharyngine)