NP-MRD: Showing NP-Card for methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate (NP0242077)

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Record Information

Version

2.0

Created at

2022-09-07 02:17:53 UTC

Updated at

2022-09-07 02:17:53 UTC

NP-MRD ID

NP0242077

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate

Description

Methyl (1S,3R,4R,10S,14S,15R,18S,19R)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]Icosa-7(20),16-diene-3-carboxylate belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom. methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate is found in Daphniphyllum calycinum. Based on a literature review very few articles have been published on methyl (1S,3R,4R,10S,14S,15R,18S,19R)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]Icosa-7(20),16-diene-3-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072204172D          

 27 32  0  0  1  0            999 V2000
   -0.0309   -2.7179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0902   -1.8951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5927   -1.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3350   -1.7922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5333   -0.6094    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1175   -0.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9630    0.8549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1209    0.6925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    1.1806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4749    2.0330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2122    2.5458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0481    2.3513    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8105    1.8958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1168    1.0275    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0027   -0.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8029   -0.0760    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4206   -0.6229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6512    0.7527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7600    1.5612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1819    2.1477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2361    1.7737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4112    1.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6662    0.5296    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5796   -0.2908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2023    0.6282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9540   -0.1686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1284   -0.1269    0.0000 C   0  0  2  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
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  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  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 12 21  1  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  1  0  0  0
 18 23  1  0  0  0  0
 14 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  6  0  0  0
  9 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  1  0  0  0
  8 27  1  0  0  0  0
  5 27  1  0  0  0  0
M  END

     RDKit          3D

 58 63  0  0  0  0  0  0  0  0999 V2000
    5.1113    2.6808   -0.3742 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7613    2.3270   -0.6071 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4052    1.0079   -0.9031 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3489    0.1889   -0.9443 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9877    0.6564   -1.1448 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1028    1.0473    0.0543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0279    0.0465    0.0564 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6772   -1.1740   -0.3522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7268   -2.4483   -0.1153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1417   -3.3549    0.6659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9859   -2.6456    1.6828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5908   -1.3590    1.2467 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1833   -1.5212   -0.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2547   -0.3316   -0.9000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3810    0.5070   -0.6514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9567    1.9127   -1.0945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6767    2.9725   -0.2953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5002    1.8922   -0.6053 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5852    2.0833    0.8731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5283    1.0505    1.6702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6947   -0.1481    1.3870 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2487   -0.3612    2.5200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0655    0.4562   -0.9317 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5848    0.4343   -2.2560 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9555   -3.0050   -0.8118 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8031   -1.7291   -0.9763 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7053   -0.7732   -1.3721 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0948    3.6302    0.1980 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5568    1.8450    0.2088 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6853    2.8272   -1.3054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6917    1.3017   -2.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7457    0.9975    0.9301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8031    2.0794   -0.1284 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5208   -4.0629    1.2406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7434   -3.9792   -0.0090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4555   -2.5499    2.6735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8432   -3.3474    1.9141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4536   -1.1631    1.9534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2435   -1.9012   -0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6856   -2.3344   -0.7178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2490    0.2130   -1.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6965    0.5044    0.4066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0290    2.0391   -2.1734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6525    2.6349    0.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0690    3.9085   -0.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7027    3.1427   -0.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8903    2.6404   -1.1135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6947    3.1141    1.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1347    1.0919    2.5921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3510   -0.6510    3.4106 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0069   -1.1441    2.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8074    0.5483    2.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9760   -0.3257   -2.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7105   -3.4625   -1.7693 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4621   -3.6335   -0.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5911   -1.8669   -1.7084 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1498   -1.4872    0.0560 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3677   -1.0216   -2.3983 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
  3  5  1  0
  5  6  1  0
  7  6  1  1
  7  8  1  0
  8  9  2  0
  9 25  1  0
 25 26  1  0
 26 27  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  1
 18 23  1  0
 23 24  1  6
 27  5  1  0
 21 12  1  0
 21  7  1  0
 23  7  1  0
 27  8  1  0
 23 14  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  5 31  1  6
  6 32  1  0
  6 33  1  0
 25 54  1  0
 25 55  1  0
 26 56  1  0
 26 57  1  0
 27 58  1  6
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  1
 13 39  1  0
 13 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  6
 17 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  6
 19 48  1  0
 20 49  1  0
 22 50  1  0
 22 51  1  0
 22 52  1  0
 24 53  1  0
M  END


  Mrv1652309072204172D          

 27 32  0  0  1  0            999 V2000
   -0.0309   -2.7179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0902   -1.8951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5927   -1.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3350   -1.7922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5333   -0.6094    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1175   -0.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9630    0.8549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1209    0.6925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    1.1806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4749    2.0330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2122    2.5458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0481    2.3513    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8105    1.8958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1168    1.0275    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0027   -0.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8029   -0.0760    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4206   -0.6229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6512    0.7527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7600    1.5612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1819    2.1477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2361    1.7737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4112    1.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6662    0.5296    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5796   -0.2908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2023    0.6282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9540   -0.1686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1284   -0.1269    0.0000 C   0  0  2  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
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  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  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 12 21  1  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  1  0  0  0
 18 23  1  0  0  0  0
 14 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  6  0  0  0
  9 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  1  0  0  0
  8 27  1  0  0  0  0
  5 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0242077

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H]1C[C@@]23C4=C(CC[C@H]14)CC[C@@H]1CN4C[C@@H](C)[C@@H](C=C[C@]21C)[C@@]34O

> <INCHI_IDENTIFIER>
InChI=1S/C23H31NO3/c1-13-11-24-12-15-6-4-14-5-7-16-17(20(25)27-3)10-22(19(14)16)21(15,2)9-8-18(13)23(22,24)26/h8-9,13,15-18,26H,4-7,10-12H2,1-3H3/t13-,15-,16-,17-,18-,21+,22-,23-/m1/s1

> <INCHI_KEY>
LRXSXOUROHJARD-ANPMZTDTSA-N

> <FORMULA>
C23H31NO3

> <MOLECULAR_WEIGHT>
369.505

> <EXACT_MASS>
369.230393862

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.181790626622096

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,3R,4R,10S,14S,15R,18S,19R)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1^{1,4}.0^{10,18}.0^{15,19}.0^{7,20}]icosa-7(20),16-diene-3-carboxylate

> <JCHEM_LOGP>
2.350429876667965

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.567487057887224

> <JCHEM_PKA_STRONGEST_BASIC>
10.61370685573856

> <JCHEM_POLAR_SURFACE_AREA>
49.769999999999996

> <JCHEM_REFRACTIVITY>
105.121

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,3R,4R,10S,14S,15R,18S,19R)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1^{1,4}.0^{10,18}.0^{15,19}.0^{7,20}]icosa-7(20),16-diene-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.058  -5.073   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.168  -3.537   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.106  -2.673   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.492  -3.346   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.996  -1.137   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.086  -0.072   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.798   1.596   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.226   1.293   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.008   2.204   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.887   3.795   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.396   4.752   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.956   4.389   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.380   3.539   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       3.951   1.918   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       3.738  -0.053   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.232  -0.142   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.385  -1.163   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.949   1.405   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.152   2.914   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.073   4.009   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.307   3.311   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.768   3.291   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.110   0.989   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.949  -0.543   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.244   1.173   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.781  -0.315   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.240  -0.237   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   27                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   21   23                                             
CONECT    8    7    9   27                                                  
CONECT    9    8   10   25                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   12    7   22                                             
CONECT   22   21                                                            
CONECT   23   18   14    7   24                                             
CONECT   24   23                                                            
CONECT   25    9   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26    8    5                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   64    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,3R,4R,10S,14S,15R,18S,19R)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1,.0,.0,.0,]icosa-7(20),16-diene-3-carboxylic acid	Generator

Chemical Formula

C₂₃H₃₁NO₃

Average Mass

369.5050 Da

Monoisotopic Mass

369.23039 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H]1C[C@@]23C4=C(CC[C@H]14)CC[C@@H]1CN4C[C@@H](C)[C@@H](C=C[C@]21C)[C@@]34O

InChI Identifier

InChI=1S/C23H31NO3/c1-13-11-24-12-15-6-4-14-5-7-16-17(20(25)27-3)10-22(19(14)16)21(15,2)9-8-18(13)23(22,24)26/h8-9,13,15-18,26H,4-7,10-12H2,1-3H3/t13-,15-,16-,17-,18-,21+,22-,23-/m1/s1

InChI Key

LRXSXOUROHJARD-ANPMZTDTSA-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
Daphniphyllum calycinum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azaspirodecane derivatives

Sub Class

Not Available

Direct Parent

Azaspirodecane derivatives

Alternative Parents

Substituents

Azaspirodecane
Indole or derivatives
Indolizidine
Piperidine
N-alkylpyrrolidine
Methyl ester
Pyrrolidine
Carboxylic acid ester
Hemiaminal
Alkanolamine
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Azacycle
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163011797

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate (NP0242077)

MOL for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)

3D MOL for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)

3D SDF for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)

3D-SDF for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)

PDB for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)

3D PDB for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)

SMILES for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)

INCHI for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)

Structure for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)

3D Structure for NP0242077 (methyl (1s,3r,4r,10s,14s,15r,18s,19r)-19-hydroxy-14,18-dimethyl-12-azahexacyclo[10.6.1.1¹,⁴.0¹⁰,¹⁸.0¹⁵,¹⁹.0⁷,²⁰]icosa-7(20),16-diene-3-carboxylate)