NP-MRD: Showing NP-Card for methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate (NP0317605)

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Record Information

Version

2.0

Created at

2022-09-11 17:35:11 UTC

Updated at

2022-09-11 17:35:11 UTC

NP-MRD ID

NP0317605

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate

Description

Methyl 6-hydroxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]Pentadecan]-8'(14')-ene-12'-carboxylate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate is found in Daphniphyllum gracile. Methyl 6-hydroxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]Pentadecan]-8'(14')-ene-12'-carboxylate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171513192D          

 29 33  0  0  0  0            999 V2000
    5.0510    2.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9028    1.5051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258    1.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4971    1.7618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9777    0.4161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2340    0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3438   -0.7587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792   -0.4068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8084   -0.9666    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9866   -0.8941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7130   -1.7493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581   -2.1251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4250   -2.6107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2205   -2.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5456   -1.6338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1554   -0.9069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5471   -0.1809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4691   -0.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3575   -1.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7220   -1.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0613   -1.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3031   -1.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2054   -0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8335    0.0857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -0.1566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6243   -0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4156   -0.8891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2272   -1.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1857   -0.3243    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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 19  1  0  0  0  0
 12 20  1  0  0  0  0
  7 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
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 20 26  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 66 70  0  0  0  0  0  0  0  0999 V2000
   -3.0724    4.6343    0.9353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6623    3.3069    0.5851 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1613    2.6446   -0.5110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0207    3.2648   -1.2219 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7274    1.2665   -0.8639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2119    1.2250   -1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8442   -0.2028   -0.8565 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9009   -1.0386   -2.1444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9809   -2.4143   -1.6833 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2062   -3.3141   -2.8149 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3150   -2.7522   -1.1392 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7583   -1.8558   -0.0363 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2191   -2.3142    1.3017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2141   -2.7975    1.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1475   -1.6764    0.8491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8339   -0.6476    0.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8666    0.4150    0.3701 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0870   -0.4459    0.4212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5744   -1.6001    1.3000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5351   -0.3918   -0.2998 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5845    0.0245   -1.3398 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7086    0.7871   -0.7420 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0835    0.4033    0.6423 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1429   -0.5347    0.6389 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    1.6549    1.3027 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8955    2.0196    0.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2017    1.2400    2.6478 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0378    0.0027    1.4428 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8108    0.4193    0.9262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3330    4.5984    2.0127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9977    4.9087    0.3726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2594    5.3604    0.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2699    0.8859   -1.7268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6858    1.9418   -0.4944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0633    1.5356   -2.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7947   -0.7368   -2.7249 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0196   -0.9453   -2.7254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1760   -3.7986   -2.6413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3670   -3.9930   -2.9873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3279   -2.7266   -3.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1051   -2.7893   -1.9396 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2531   -3.7883   -0.7459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8804   -1.9803    0.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2575   -1.5419    2.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8171   -3.1792    1.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3401   -3.6336    0.5219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5030   -3.1114    2.2327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7037    0.9517    1.3009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9580    0.0399    0.8950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3179   -0.8799   -0.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6749   -1.3445    2.3543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1235   -2.5475    1.0285 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9607   -0.8754   -1.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0501    0.7162   -2.0485 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6150    0.6143   -1.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370    1.9010   -0.8185 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2738   -0.9326   -0.2401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9688    2.4823    1.3238 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3328    1.0836   -0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6400    2.7478   -0.3414 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6797    2.4182    1.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1545    0.6838    2.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5191    0.5319    3.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3794    2.1498    3.2409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9823    1.4829    0.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0059    0.4476    1.6554 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  6
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 12 20  1  0
 20 21  1  6
 21 22  1  0
 22 23  1  0
 23 24  1  6
 23 28  1  0
 28 29  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 17  5  1  0
 29 20  1  0
 16  7  1  0
 20  7  1  0
 19 15  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  6
  6 34  1  0
  6 35  1  0
  8 36  1  0
  8 37  1  0
 10 38  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  1
 13 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 17 48  1  1
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 24 57  1  0
 29 65  1  0
 29 66  1  0
 25 58  1  0
 26 59  1  0
 26 60  1  0
 26 61  1  0
 27 62  1  0
 27 63  1  0
 27 64  1  0
M  END


  Mrv1533004171513192D          

 29 33  0  0  0  0            999 V2000
    5.0510    2.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9028    1.5051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258    1.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4971    1.7618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9777    0.4161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2340    0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3438   -0.7587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792   -0.4068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8084   -0.9666    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9866   -0.8941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7130   -1.7493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581   -2.1251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4250   -2.6107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2205   -2.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5456   -1.6338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1554   -0.9069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5471   -0.1809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4691   -0.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3575   -1.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7220   -1.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0613   -1.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3031   -1.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2054   -0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8335    0.0857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -0.1566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6243   -0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4156   -0.8891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2272   -1.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1857   -0.3243    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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 19  1  0  0  0  0
 12 20  1  0  0  0  0
  7 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
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 20 26  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0317605

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1CC23CN(C)CC(CCC4=C2C1CC4)C31CCC(O)(OC1)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C24H37NO4/c1-15(2)24(27)10-9-22(14-29-24)17-7-5-16-6-8-18-19(21(26)28-4)11-23(22,20(16)18)13-25(3)12-17/h15,17-19,27H,5-14H2,1-4H3

> <INCHI_KEY>
OUGJTNKMUCIUKC-UHFFFAOYSA-N

> <FORMULA>
C24H37NO4

> <MOLECULAR_WEIGHT>
403.563

> <EXACT_MASS>
403.272258675

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
45.654384584056416

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 6-hydroxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate

> <ALOGPS_LOGP>
2.42

> <JCHEM_LOGP>
2.458727443605137

> <ALOGPS_LOGS>
-3.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.879567082455125

> <JCHEM_PKA_STRONGEST_BASIC>
10.07932962338062

> <JCHEM_POLAR_SURFACE_AREA>
59.0

> <JCHEM_REFRACTIVITY>
112.57229999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.30e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       9.428   4.324   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.152   2.810   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.702   2.292   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.528   3.289   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.425   0.777   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.037   0.110   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.242  -1.416   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.254  -0.759   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       3.376  -1.804   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       1.842  -1.669   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.198  -3.265   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.148  -3.967   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.393  -4.873   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.878  -4.465   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.485  -3.050   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.757  -1.693   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.488  -0.338   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.209  -1.251   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.001  -2.777   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.081  -2.428   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.848  -3.351   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.432  -2.744   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.250  -1.215   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.556   0.160   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       3.483  -0.292   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.899  -0.899   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.776  -1.660   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.424  -3.159   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.347  -0.605   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   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   16   20                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15    7   17                                                  
CONECT   17   16    5   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   15                                                       
CONECT   20   12    7   21   26                                             
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   27                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   20                                                       
CONECT   27   23   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Value	Source
Methyl 6-hydroxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1,.0,]pentadecan]-8'(14')-ene-12'-carboxylic acid	Generator
Methyl 6-hydroxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylic acid	Generator

Chemical Formula

C₂₄H₃₇NO₄

Average Mass

403.5630 Da

Monoisotopic Mass

403.27226 Da

IUPAC Name

methyl 6-hydroxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate

Traditional Name

methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1CC23CN(C)CC(CCC4=C2C1CC4)C31CCC(O)(OC1)C(C)C

InChI Identifier

InChI=1S/C24H37NO4/c1-15(2)24(27)10-9-22(14-29-24)17-7-5-16-6-8-18-19(21(26)28-4)11-23(22,20(16)18)13-25(3)12-17/h15,17-19,27H,5-14H2,1-4H3

InChI Key

OUGJTNKMUCIUKC-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Daphniphyllum gracile	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Azaspirodecane
Oxane
Piperidine
Methyl ester
Amino acid or derivatives
Carboxylic acid ester
Hemiacetal
Tertiary amine
Tertiary aliphatic amine
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Azacycle
Oxacycle
Organic nitrogen compound
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Amine
Carbonyl group
Hydrocarbon derivative
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
logP	2.42	ALOGPS
logP	2.46	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	11.88	ChemAxon
pKa (Strongest Basic)	10.08	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	59 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	112.57 m³·mol⁻¹	ChemAxon
Polarizability	45.65 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

74007478

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate (NP0317605)

MOL for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D MOL for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D SDF for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D-SDF for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

PDB for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D PDB for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

SMILES for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

INCHI for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

Structure for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D Structure for NP0317605 (methyl 6-hydroxy-6-isopropyl-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)