NP-MRD: Showing NP-Card for (7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one (NP0325824)

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Record Information

Version

2.0

Created at

2022-09-12 06:52:51 UTC

Updated at

2022-09-12 06:52:51 UTC

NP-MRD ID

NP0325824

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one

Description

Caesalpinine A belongs to the class of organic compounds known as hybrid peptides. Hybrid peptides are compounds containing at least two different types of amino acids (alpha, beta, gamma, delta) linked to each other through a peptide bond. Based on a literature review very few articles have been published on Caesalpinine A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122208522D          

 31 34  0  0  1  0            999 V2000
    0.8124   -2.6058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5471   -2.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6755   -1.4157    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0620   -0.8641    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2329   -0.0570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2775   -1.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1066   -1.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6779   -2.1822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2913   -1.6306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1204   -0.8235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3359   -0.5680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5048   -1.1930    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0235   -0.5514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9205   -0.6530    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6120   -0.2030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6545    0.6209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2536   -0.7216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9586   -1.4921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7835   -1.5093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2108   -0.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0356   -0.8208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4331   -1.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0058   -2.2494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1810   -2.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2460   -2.3479    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7274   -2.9895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9125   -2.8612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938   -3.5028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5789   -3.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2825   -2.6045    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8012   -1.9629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
  3 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  0  0  0  0
 12 31  1  1  0  0  0
M  END

     RDKit          3D

 62 65  0  0  0  0  0  0  0  0999 V2000
    2.7785   -1.2662    1.8474 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1967   -0.9041    0.7942 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2095    0.4623    0.1466 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4601    0.6504   -0.6316 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7708   -0.3639   -1.5197 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6365    0.9421    0.2677 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0079    2.2197    0.6076 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0837    2.4800    1.4199 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8147    1.4206    1.9100 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4731    0.1223    1.5910 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3700   -0.1076    0.7598 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9736    0.3471   -0.6698 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6909    1.3733   -1.6847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4275    2.2242   -1.3059 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5817    1.8458   -0.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2076    2.4079    0.1567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2885    0.7801   -1.6695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1302   -0.0878   -0.8118 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4004    0.5476   -0.4119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8136    1.7599   -0.8989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0333    2.2711   -0.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8426    1.6045    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4221    0.3851    0.9395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2238   -0.1260    0.5105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4669   -0.5712    0.3695 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1825   -1.9681    0.3880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0865   -2.2111    1.3915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1926   -3.3577    1.1029 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9143   -3.1363    0.1477 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3983   -1.7897    0.0253 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0231   -1.0600   -1.1701 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0866    1.2420    0.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3790    1.5792   -1.2769 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0050   -1.2157   -1.1112 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4008    3.0397    0.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3429    3.5186    1.6645 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6630    1.6568    2.5522 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0647   -0.6886    1.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1748   -1.1483    0.5568 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1246    0.4144    0.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5181    0.8903   -2.6698 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5476    2.0605   -1.8066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1391    1.8884    1.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9161    1.2641   -2.4421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5663    0.1740   -2.2912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4069   -0.9779   -1.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2559    2.3527   -1.6083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3493    3.2257   -0.8460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7868    2.0087    0.7898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0063   -0.1743    1.6440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9031   -1.0805    0.8942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0436   -0.3314    1.1967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0594   -2.5988    0.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9419   -2.3883   -0.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5955   -2.4265    2.3789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4826   -1.3001    1.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2113   -3.7251    2.0711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8222   -4.1995    0.7001 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6746   -3.5509   -0.8505 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7996   -3.7498    0.4908 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0239   -1.4119   -1.5445 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7569   -1.2419   -1.9478 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0
  4  3  1  0
  3 12  1  0
 12 31  1  0
 31 30  1  0
 30 29  1  0
 29 28  1  0
 28 27  1  0
 27 26  1  0
 26 25  1  0
 25 18  1  0
 18 17  1  0
 17 15  1  0
 15 16  1  0
 15 14  2  0
 14 13  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 30  2  1  0
  2  1  2  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  2  3  1  0
 11  6  1  0
 13 12  1  0
 24 19  1  0
  5 34  1  0
  4 33  1  6
  3 32  1  1
 12 40  1  1
 31 61  1  0
 31 62  1  0
 29 59  1  0
 29 60  1  0
 28 57  1  0
 28 58  1  0
 27 55  1  0
 27 56  1  0
 26 53  1  0
 26 54  1  0
 25 52  1  0
 18 46  1  6
 17 44  1  0
 17 45  1  0
 16 43  1  0
 13 41  1  0
 13 42  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 23 50  1  0
 24 51  1  0
  7 35  1  0
  8 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
M  END


  Mrv1652309122208522D          

 31 34  0  0  1  0            999 V2000
    0.8124   -2.6058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5471   -2.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6755   -1.4157    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0620   -0.8641    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2329   -0.0570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2775   -1.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1066   -1.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6779   -2.1822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2913   -1.6306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1204   -0.8235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3359   -0.5680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5048   -1.1930    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0235   -0.5514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9205   -0.6530    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6120   -0.2030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6545    0.6209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2536   -0.7216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9586   -1.4921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7835   -1.5093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2108   -0.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0356   -0.8208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4331   -1.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0058   -2.2494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1810   -2.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2460   -2.3479    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7274   -2.9895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9125   -2.8612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938   -3.5028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5789   -3.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2825   -2.6045    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8012   -1.9629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
  3 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  0  0  0  0
 12 31  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0325824

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]([C@H]1[C@@H]2CN(CCCCN[C@H](CC(O)=NC2)C2=CC=CC=C2)C1=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H31N3O3/c29-22-15-21(18-9-3-1-4-10-18)26-13-7-8-14-28-17-20(16-27-22)23(25(28)31)24(30)19-11-5-2-6-12-19/h1-6,9-12,20-21,23-24,26,30H,7-8,13-17H2,(H,27,29)/t20-,21+,23+,24+/m0/s1

> <INCHI_KEY>
SHBCCFGHZDXOET-XWVZOOPGSA-N

> <FORMULA>
C25H31N3O3

> <MOLECULAR_WEIGHT>
421.541

> <EXACT_MASS>
421.23654187

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
46.16151307984047

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(7R,12S,13R)-9-hydroxy-13-[(S)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one

> <JCHEM_LOGP>
-0.2630384168219096

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.992261279270917

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6594541922004744

> <JCHEM_PKA_STRONGEST_BASIC>
8.465461696836242

> <JCHEM_POLAR_SURFACE_AREA>
85.16

> <JCHEM_REFRACTIVITY>
120.3686

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(7R,12S,13R)-9-hydroxy-13-[(S)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  O   UNK     0       1.516  -4.864   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.888  -4.164   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.128  -2.643   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.982  -1.613   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.301  -0.106   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.518  -2.090   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.199  -3.596   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.265  -4.073   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.411  -3.044   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.091  -1.537   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.627  -1.060   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.676  -2.227   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.644  -1.029   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       7.318  -1.219   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       8.609  -0.379   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.688   1.159   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.807  -1.347   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.256  -2.785   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.796  -2.817   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.593  -1.500   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.133  -1.532   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.875  -2.882   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.077  -4.199   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.538  -4.167   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       9.793  -4.383   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       8.824  -5.580   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.303  -5.341   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.335  -6.539   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.814  -6.299   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       4.261  -4.862   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       5.229  -3.664   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4   12                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    6                                                       
CONECT   12    3   13   31                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   25                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   18   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    2   31                                                  
CONECT   31   30   12                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₁N₃O₃

Average Mass

421.5410 Da

Monoisotopic Mass

421.23654 Da

IUPAC Name

(7R,12S,13R)-9-hydroxy-13-[(S)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one

Traditional Name

(7R,12S,13R)-9-hydroxy-13-[(S)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one

CAS Registry Number

Not Available

SMILES

O[C@@H]([C@H]1[C@@H]2CN(CCCCN[C@H](CC(O)=NC2)C2=CC=CC=C2)C1=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C25H31N3O3/c29-22-15-21(18-9-3-1-4-10-18)26-13-7-8-14-28-17-20(16-27-22)23(25(28)31)24(30)19-11-5-2-6-12-19/h1-6,9-12,20-21,23-24,26,30H,7-8,13-17H2,(H,27,29)/t20-,21+,23+,24+/m0/s1

InChI Key

SHBCCFGHZDXOET-XWVZOOPGSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hybrid peptides. Hybrid peptides are compounds containing at least two different types of amino acids (alpha, beta, gamma, delta) linked to each other through a peptide bond.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Hybrid peptides

Direct Parent

Hybrid peptides

Alternative Parents

Substituents

Cyclic hybrid peptide
Macrolactam
Beta amino acid or derivatives
Aralkylamine
Monocyclic benzene moiety
Pyrrolidone
2-pyrrolidone
N-alkylpyrrolidine
Benzenoid
Tertiary carboxylic acid amide
Pyrrolidine
Secondary carboxylic acid amide
Secondary alcohol
Amino acid or derivatives
Carboxamide group
Lactam
Azacycle
Organoheterocyclic compound
Secondary amine
Carboxylic acid derivative
Secondary aliphatic amine
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Amine
Carbonyl group
Organic nitrogen compound
Alcohol
Aromatic alcohol
Organic oxide
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	-0.26	ChemAxon
pKa (Strongest Acidic)	3.66	ChemAxon
pKa (Strongest Basic)	8.47	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	85.16 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	120.37 m³·mol⁻¹	ChemAxon
Polarizability	46.16 Å³	ChemAxon
Number of Rings	4	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

4572787

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5458904

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one (NP0325824)

MOL for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)

3D MOL for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)

3D SDF for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)

3D-SDF for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)

PDB for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)

3D PDB for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)

SMILES for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)

INCHI for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)

Structure for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)

3D Structure for NP0325824 ((7r,12s,13r)-9-hydroxy-13-[(s)-hydroxy(phenyl)methyl]-7-phenyl-1,6,10-triazabicyclo[10.2.1]pentadec-9-en-14-one)