NP-MRD: Showing NP-Card for (2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one (NP0171810)

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Record Information

Version

2.0

Created at

2022-09-03 08:29:00 UTC

Updated at

2022-09-03 08:29:00 UTC

NP-MRD ID

NP0171810

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one

Description

Spirofornabuxine belongs to the class of organic compounds known as cyclic ketones. These are organic compounds containing a ketone that is conjugated to a cyclic moiety. (2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one is found in Buxus sempervirens. (2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one was first documented in 2010 (PMID: 20655557). Based on a literature review very few articles have been published on Spirofornabuxine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032210292D          

 27 31  0  0  1  0            999 V2000
   -0.5685   -0.1412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1020    0.3395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8536   -0.0009    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5241    0.4798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2756    0.1395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3670    0.9594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0314    0.4703    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5795   -0.1463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3961   -0.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9973   -0.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9304   -1.4157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2458   -1.8761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4591   -1.6280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1625   -0.8581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3566   -0.6815    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5231   -1.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6861   -1.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9346   -0.8219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2641   -1.3026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2099    0.2037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0337    0.2478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3302   -0.5220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1274   -0.7346    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7101   -0.1506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6897   -1.0420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1326   -1.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3237   -1.7813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  6  1  6  0  0  0
  5  7  1  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  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  2  0  0  0  0
 10 20  1  0  0  0  0
 20 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
 22 25  1  0  0  0  0
 10 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 62 66  0  0  0  0  0  0  0  0999 V2000
    7.0737    0.1709   -0.6570 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0619   -0.4769    0.2650 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8801   -0.9368   -0.5335 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8040   -1.6033    0.2954 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4818   -1.0520   -0.1858 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8092   -1.7623   -1.2973 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1769   -1.6100    0.1036 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1939   -0.4743    0.0814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1022   -0.5781    0.2096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2450    0.3384    0.2221 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0276    1.6822   -0.2843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9227    2.3582   -0.5323 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4645    1.9590   -0.3709 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9407    0.7437   -0.1074 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3762    0.4052    0.0648 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6950    0.7953    1.4980 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2795    1.1113   -0.9155 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3523    0.1764   -1.3605 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8168    0.3600   -2.4931 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7492    0.3844    1.6564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2267    0.5513    1.5729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6130    0.4446    0.1221 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8677   -0.2995   -0.0300 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9404    0.4382    0.6212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4452   -0.2318   -0.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3516    0.1086   -2.0070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5846   -1.7127   -0.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9743   -0.1803   -1.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9119    1.2867   -0.6899 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0869    0.0074   -0.2632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7408    0.3148    0.9697 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5195   -1.2653    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2900   -1.7142   -1.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7626   -2.7089    0.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9596   -1.5608    1.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2068   -2.7915   -1.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3528   -1.2753   -2.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9562   -2.5076    0.6780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4049   -1.6221    0.3480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9781    2.2127   -0.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0883    3.3627   -0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2362    2.7263   -0.4724 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8005    1.9024    1.4924 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5641    0.3156    1.9272 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7995    0.5561    2.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6897    1.4914   -1.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7746    1.9400   -0.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5079   -0.5988    2.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2346    1.1527    2.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7596   -0.2945    2.0958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5890    1.4926    2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8353    1.4412   -0.3256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7677   -1.1772    0.5537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8924   -0.0300    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8418    0.4569    1.7235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9825    1.4939    0.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3774    0.0677   -2.4118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9478    1.1048   -2.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7616   -0.7107   -2.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6189   -1.9889    0.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5849   -1.9736   -0.8492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7838   -2.2165   -0.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  5  4  1  1
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
 10  9  1  1
 10 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  1  0
 18 19  2  0
 18  3  1  0
  7  5  1  0
 14  8  1  0
 15  5  1  0
 25 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  6
  4 34  1  0
  4 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  1
  9 39  1  0
 20 48  1  0
 20 49  1  0
 21 50  1  0
 21 51  1  0
 22 52  1  6
 23 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 26 57  1  0
 26 58  1  0
 26 59  1  0
 27 60  1  0
 27 61  1  0
 27 62  1  0
 11 40  1  0
 12 41  1  0
 13 42  1  0
 16 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
M  END


  Mrv1652309032210292D          

 27 31  0  0  1  0            999 V2000
   -0.5685   -0.1412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1020    0.3395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8536   -0.0009    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5241    0.4798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2756    0.1395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3670    0.9594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0314    0.4703    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5795   -0.1463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3961   -0.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9973   -0.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9304   -1.4157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2458   -1.8761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4591   -1.6280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1625   -0.8581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3566   -0.6815    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5231   -1.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6861   -1.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9346   -0.8219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2641   -1.3026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2099    0.2037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0337    0.2478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3302   -0.5220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1274   -0.7346    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7101   -0.1506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6897   -1.0420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1326   -1.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3237   -1.7813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  6  1  6  0  0  0
  5  7  1  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  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  2  0  0  0  0
 10 20  1  0  0  0  0
 20 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
 22 25  1  0  0  0  0
 10 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171810

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1C[C@@]23C[C@@H]2C2=CC4(CCC(NC)C4(C)C)C=CC=C2[C@]3(C)CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H35NO/c1-6-16-12-25-14-19(25)17-13-24(11-9-21(26-5)22(24,2)3)10-7-8-18(17)23(25,4)15-20(16)27/h7-8,10,13,16,19,21,26H,6,9,11-12,14-15H2,1-5H3/t16-,19+,21?,23-,24?,25+/m0/s1

> <INCHI_KEY>
DAQJYUCPSHWKIR-IBCHWLJGSA-N

> <FORMULA>
C25H35NO

> <MOLECULAR_WEIGHT>
365.561

> <EXACT_MASS>
365.271864751

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.679339508909976

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2'S,4'S,6'S,9'R)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0^{2,4}.0^{4,9}]pentadecane]-1'(15'),10',12'-trien-7'-one

> <ALOGPS_LOGP>
5.53

> <JCHEM_LOGP>
3.9748179873333336

> <ALOGPS_LOGS>
-5.13

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
10.658711297443663

> <JCHEM_POLAR_SURFACE_AREA>
29.1

> <JCHEM_REFRACTIVITY>
113.72389999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.69e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2'S,4'S,6'S,9'R)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0^{2,4}.0^{4,9}]pentadecane]-1'(15'),10',12'-trien-7'-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.061  -0.264   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.190   0.634   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.593  -0.002   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.845   0.896   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.248   0.260   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.418   1.791   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.659   0.878   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.682  -0.273   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.206  -0.053   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.328  -1.108   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.203  -2.643   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.926  -3.502   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.457  -3.039   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.903  -1.602   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.399  -1.272   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.710  -2.780   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.147  -2.169   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.745  -1.534   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.493  -2.431   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.725   0.380   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.263   0.463   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.816  -0.974   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      13.304  -1.371   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0      14.392  -0.281   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.621  -1.945   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.447  -3.244   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.938  -3.325   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   15                                             
CONECT    6    5    7                                                       
CONECT    7    6    5    8                                                  
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   20   25                                             
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    8   15                                                  
CONECT   15   14    5   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    3   19                                                  
CONECT   19   18                                                            
CONECT   20   10   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   10   26   27                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₅NO

Average Mass

365.5610 Da

Monoisotopic Mass

365.27186 Da

IUPAC Name

(2'S,4'S,6'S,9'R)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0^{2,4}.0^{4,9}]pentadecane]-1'(15'),10',12'-trien-7'-one

Traditional Name

(2'S,4'S,6'S,9'R)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0^{2,4}.0^{4,9}]pentadecane]-1'(15'),10',12'-trien-7'-one

CAS Registry Number

Not Available

SMILES

CC[C@H]1C[C@@]23C[C@@H]2C2=CC4(CCC(NC)C4(C)C)C=CC=C2[C@]3(C)CC1=O

InChI Identifier

InChI=1S/C25H35NO/c1-6-16-12-25-14-19(25)17-13-24(11-9-21(26-5)22(24,2)3)10-7-8-18(17)23(25,4)15-20(16)27/h7-8,10,13,16,19,21,26H,6,9,11-12,14-15H2,1-5H3/t16-,19+,21?,23-,24?,25+/m0/s1

InChI Key

DAQJYUCPSHWKIR-IBCHWLJGSA-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
Buxus sempervirens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic ketones. These are organic compounds containing a ketone that is conjugated to a cyclic moiety.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Cyclic ketones

Alternative Parents

Substituents

Cyclic ketone
Secondary amine
Secondary aliphatic amine
Organic nitrogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Amine
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	5.53	ALOGPS
logP	3.97	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Basic)	10.66	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.1 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	113.72 m³·mol⁻¹	ChemAxon
Polarizability	44.68 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00029040

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

101701610

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ata A, Iverson CD, Kalhari KS, Akhter S, Betteridge J, Meshkatalsadat MH, Orhan I, Sener B: Triterpenoidal alkaloids from Buxus hyrcana and their enzyme inhibitory, anti-fungal and anti-leishmanial activities. Phytochemistry. 2010 Oct;71(14-15):1780-6. doi: 10.1016/j.phytochem.2010.06.017. Epub 2010 Jul 23. [PubMed:20655557 ]
LOTUS database [Link]

Showing NP-Card for (2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one (NP0171810)

MOL for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)

3D MOL for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)

3D SDF for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)

3D-SDF for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)

PDB for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)

3D PDB for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)

SMILES for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)

INCHI for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)

Structure for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)

3D Structure for NP0171810 ((2's,4's,6's,9'r)-6'-ethyl-2,2,9'-trimethyl-3-(methylamino)spiro[cyclopentane-1,14'-tetracyclo[8.5.0.0²,⁴.0⁴,⁹]pentadecane]-1'(15'),10',12'-trien-7'-one)