NP-MRD: Showing NP-Card for hortonone A (NP0036811)

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Record Information

Version

2.0

Created at

2021-06-20 19:53:12 UTC

Updated at

2021-06-30 00:08:40 UTC

NP-MRD ID

NP0036811

Secondary Accession Numbers

None

Natural Product Identification

Common Name

hortonone A

Provided By

JEOL Database JEOL Logo

Description

Rel-Hortonone A belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol. hortonone A is found in Hortonia. hortonone A was first documented in 2012 (Carr, G., et al.). Based on a literature review very few articles have been published on Rel-Hortonone A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121533D          

 40 41  0  0  0  0            999 V2000
   -1.7479    0.8366   -4.7851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734    0.7161   -3.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4888   -0.3163   -3.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0287   -0.6025   -1.6219 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0610   -1.1509   -1.4715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9733   -0.2634   -0.4697 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5984   -1.0374    0.7952 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2887   -0.1044    1.6143 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3421    1.2520    0.8732 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5402    2.4325    1.8650 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6094    3.8002    1.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8257    2.2450    2.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9215    1.2259   -0.0505 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2070    1.5814    0.7338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7936    2.1711   -1.2698 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7151    1.8480   -2.4568 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4308   -0.0108   -5.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3513    1.7485   -5.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8417    0.8771   -4.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1415   -1.0427   -3.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9799   -0.5725   -0.7807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1008   -1.9920    0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5028   -1.2717    1.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1283   -0.0025    2.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2960   -0.5233    1.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2302    1.2229    0.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2965    2.4530    2.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3096    3.7930    0.3418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3721    4.1157    0.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    4.5739    1.8861 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7869    1.3375    3.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9735    3.0844    3.3773 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7053    2.1826    2.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3010    1.0049    1.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2300    2.6406    1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1040    1.3815    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2458    2.2042   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0292    3.1950   -0.9619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7434    1.6676   -2.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7506    2.7604   -3.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  6  1  0  0  0  0
 13  9  1  0  0  0  0
  9  8  1  0  0  0  0
  8  7  1  0  0  0  0
  7  6  1  0  0  0  0
 13 15  1  0  0  0  0
  4  5  2  0  0  0  0
 16 15  1  0  0  0  0
  2  1  1  0  0  0  0
  6 13  1  0  0  0  0
  6 21  1  6  0  0  0
 13 14  1  1  0  0  0
  3  2  2  0  0  0  0
  9 10  1  0  0  0  0
  3  4  1  0  0  0  0
 10 11  1  0  0  0  0
  2 16  1  0  0  0  0
 10 12  1  0  0  0  0
  3 20  1  0  0  0  0
 16 39  1  0  0  0  0
 16 40  1  0  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
  9 26  1  6  0  0  0
  8 24  1  0  0  0  0
  8 25  1  0  0  0  0
  7 22  1  0  0  0  0
  7 23  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
 14 34  1  0  0  0  0
 14 35  1  0  0  0  0
 14 36  1  0  0  0  0
 10 27  1  1  0  0  0
 11 28  1  0  0  0  0
 11 29  1  0  0  0  0
 11 30  1  0  0  0  0
 12 31  1  0  0  0  0
 12 32  1  0  0  0  0
 12 33  1  0  0  0  0
M  END

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
   -1.7479    0.8366   -4.7851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734    0.7161   -3.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4888   -0.3163   -3.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0287   -0.6025   -1.6219 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0610   -1.1509   -1.4715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9733   -0.2634   -0.4697 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5984   -1.0374    0.7952 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2887   -0.1044    1.6143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3421    1.2520    0.8732 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5402    2.4325    1.8650 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6094    3.8002    1.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8257    2.2450    2.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9215    1.2259   -0.0505 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2070    1.5814    0.7338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7936    2.1711   -1.2698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7151    1.8480   -2.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4308   -0.0108   -5.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3513    1.7485   -5.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8417    0.8771   -4.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1415   -1.0427   -3.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9799   -0.5725   -0.7807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1008   -1.9920    0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5028   -1.2717    1.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1283   -0.0025    2.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2960   -0.5233    1.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2302    1.2229    0.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2965    2.4530    2.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3096    3.7930    0.3418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3721    4.1157    0.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    4.5739    1.8861 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7869    1.3375    3.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9735    3.0844    3.3773 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7053    2.1826    2.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3010    1.0049    1.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2300    2.6406    1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1040    1.3815    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2458    2.2042   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0292    3.1950   -0.9619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7434    1.6676   -2.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7506    2.7604   -3.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  6  1  0
 13  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
 13 15  1  0
  4  5  2  0
 16 15  1  0
  2  1  1  0
  6 13  1  0
  6 21  1  6
 13 14  1  1
  3  2  2  0
  9 10  1  0
  3  4  1  0
 10 11  1  0
  2 16  1  0
 10 12  1  0
  3 20  1  0
 16 39  1  0
 16 40  1  0
 15 37  1  0
 15 38  1  0
  9 26  1  6
  8 24  1  0
  8 25  1  0
  7 22  1  0
  7 23  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 10 27  1  1
 11 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
M  END


  Mrv1652306202121533D          

 40 41  0  0  0  0            999 V2000
   -1.7479    0.8366   -4.7851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734    0.7161   -3.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4888   -0.3163   -3.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0287   -0.6025   -1.6219 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0610   -1.1509   -1.4715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9733   -0.2634   -0.4697 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5984   -1.0374    0.7952 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2887   -0.1044    1.6143 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3421    1.2520    0.8732 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5402    2.4325    1.8650 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6094    3.8002    1.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8257    2.2450    2.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9215    1.2259   -0.0505 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2070    1.5814    0.7338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7936    2.1711   -1.2698 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7151    1.8480   -2.4568 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4308   -0.0108   -5.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3513    1.7485   -5.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8417    0.8771   -4.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1415   -1.0427   -3.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9799   -0.5725   -0.7807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1008   -1.9920    0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5028   -1.2717    1.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1283   -0.0025    2.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2960   -0.5233    1.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2302    1.2229    0.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2965    2.4530    2.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3096    3.7930    0.3418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3721    4.1157    0.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    4.5739    1.8861 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7869    1.3375    3.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9735    3.0844    3.3773 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7053    2.1826    2.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3010    1.0049    1.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2300    2.6406    1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1040    1.3815    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2458    2.2042   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0292    3.1950   -0.9619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7434    1.6676   -2.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7506    2.7604   -3.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  6  1  0  0  0  0
 13  9  1  0  0  0  0
  9  8  1  0  0  0  0
  8  7  1  0  0  0  0
  7  6  1  0  0  0  0
 13 15  1  0  0  0  0
  4  5  2  0  0  0  0
 16 15  1  0  0  0  0
  2  1  1  0  0  0  0
  6 13  1  0  0  0  0
  6 21  1  6  0  0  0
 13 14  1  1  0  0  0
  3  2  2  0  0  0  0
  9 10  1  0  0  0  0
  3  4  1  0  0  0  0
 10 11  1  0  0  0  0
  2 16  1  0  0  0  0
 10 12  1  0  0  0  0
  3 20  1  0  0  0  0
 16 39  1  0  0  0  0
 16 40  1  0  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
  9 26  1  6  0  0  0
  8 24  1  0  0  0  0
  8 25  1  0  0  0  0
  7 22  1  0  0  0  0
  7 23  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
 14 34  1  0  0  0  0
 14 35  1  0  0  0  0
 14 36  1  0  0  0  0
 10 27  1  1  0  0  0
 11 28  1  0  0  0  0
 11 29  1  0  0  0  0
 11 30  1  0  0  0  0
 12 31  1  0  0  0  0
 12 32  1  0  0  0  0
 12 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0036811

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@@]([H])(C1=O)C([H])([H])C([H])([H])[C@]2([H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O/c1-10(2)12-5-6-13-14(16)9-11(3)7-8-15(12,13)4/h9-10,12-13H,5-8H2,1-4H3/t12-,13-,15-/m1/s1

> <INCHI_KEY>
YJMPMKVSGMSRFT-UMVBOHGHSA-N

> <FORMULA>
C15H24O

> <MOLECULAR_WEIGHT>
220.356

> <EXACT_MASS>
220.182715393

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
26.818896847072768

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3aS,8aR)-6,8a-dimethyl-1-(propan-2-yl)-1,2,3,3a,4,7,8,8a-octahydroazulen-4-one

> <ALOGPS_LOGP>
3.86

> <JCHEM_LOGP>
4.303449805666666

> <ALOGPS_LOGS>
-4.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.455690186871458

> <JCHEM_PKA_STRONGEST_BASIC>
-4.563376039901087

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
68.3189

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.60e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3aS,8aR)-1-isopropyl-6,8a-dimethyl-1,2,3,3a,7,8-hexahydroazulen-4-one

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
   -1.7479    0.8366   -4.7851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734    0.7161   -3.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4888   -0.3163   -3.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0287   -0.6025   -1.6219 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0610   -1.1509   -1.4715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9733   -0.2634   -0.4697 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5984   -1.0374    0.7952 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2887   -0.1044    1.6143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3421    1.2520    0.8732 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5402    2.4325    1.8650 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6094    3.8002    1.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8257    2.2450    2.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9215    1.2259   -0.0505 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2070    1.5814    0.7338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7936    2.1711   -1.2698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7151    1.8480   -2.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4308   -0.0108   -5.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3513    1.7485   -5.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8417    0.8771   -4.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1415   -1.0427   -3.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9799   -0.5725   -0.7807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1008   -1.9920    0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5028   -1.2717    1.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1283   -0.0025    2.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2960   -0.5233    1.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2302    1.2229    0.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2965    2.4530    2.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3096    3.7930    0.3418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3721    4.1157    0.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    4.5739    1.8861 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7869    1.3375    3.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9735    3.0844    3.3773 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7053    2.1826    2.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3010    1.0049    1.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2300    2.6406    1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1040    1.3815    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2458    2.2042   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0292    3.1950   -0.9619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7434    1.6676   -2.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7506    2.7604   -3.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  6  1  0
 13  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
 13 15  1  0
  4  5  2  0
 16 15  1  0
  2  1  1  0
  6 13  1  0
  6 21  1  6
 13 14  1  1
  3  2  2  0
  9 10  1  0
  3  4  1  0
 10 11  1  0
  2 16  1  0
 10 12  1  0
  3 20  1  0
 16 39  1  0
 16 40  1  0
 15 37  1  0
 15 38  1  0
  9 26  1  6
  8 24  1  0
  8 25  1  0
  7 22  1  0
  7 23  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 10 27  1  1
 11 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.748   0.837  -4.785  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.273   0.716  -3.359  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.489  -0.316  -3.005  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.029  -0.603  -1.622  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.061  -1.151  -1.472  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.973  -0.263  -0.470  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.598  -1.037   0.795  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.289  -0.104   1.614  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.342   1.252   0.873  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.540   2.433   1.865  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.609   3.800   1.183  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.826   2.245   2.689  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.922   1.226  -0.051  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.207   1.581   0.734  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.794   2.171  -1.270  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.715   1.848  -2.457  0.00  0.00           C+0
HETATM   17  H   UNK     0      -1.431  -0.011  -5.402  0.00  0.00           H+0
HETATM   18  H   UNK     0      -1.351   1.749  -5.243  0.00  0.00           H+0
HETATM   19  H   UNK     0      -2.842   0.877  -4.816  0.00  0.00           H+0
HETATM   20  H   UNK     0      -0.142  -1.043  -3.734  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.980  -0.573  -0.781  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.101  -1.992   0.595  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.503  -1.272   1.370  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.128  -0.003   2.623  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.296  -0.523   1.719  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.230   1.223   0.224  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.297   2.453   2.574  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.310   3.793   0.342  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.372   4.116   0.824  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.939   4.574   1.886  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.787   1.337   3.299  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.974   3.084   3.377  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.705   2.183   2.039  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.301   1.005   1.660  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.230   2.641   1.009  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.104   1.381   0.138  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.246   2.204  -1.622  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.029   3.195  -0.962  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.743   1.668  -2.125  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.751   2.760  -3.068  0.00  0.00           H+0
CONECT    1    2   17   18   19                                             
CONECT    2    1    3   16                                                  
CONECT    3    2    4   20                                                  
CONECT    4    6    5    3                                                  
CONECT    5    4                                                            
CONECT    6    4    7   13   21                                             
CONECT    7    8    6   22   23                                             
CONECT    8    9    7   24   25                                             
CONECT    9   13    8   10   26                                             
CONECT   10    9   11   12   27                                             
CONECT   11   10   28   29   30                                             
CONECT   12   10   31   32   33                                             
CONECT   13    9   15    6   14                                             
CONECT   14   13   34   35   36                                             
CONECT   15   13   16   37   38                                             
CONECT   16   15    2   39   40                                             
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    3                                                            
CONECT   21    6                                                            
CONECT   22    7                                                            
CONECT   23    7                                                            
CONECT   24    8                                                            
CONECT   25    8                                                            
CONECT   26    9                                                            
CONECT   27   10                                                            
CONECT   28   11                                                            
CONECT   29   11                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   12                                                            
CONECT   33   12                                                            
CONECT   34   14                                                            
CONECT   35   14                                                            
CONECT   36   14                                                            
CONECT   37   15                                                            
CONECT   38   15                                                            
CONECT   39   16                                                            
CONECT   40   16                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   82    0
END

RDKit          3D

40 41  0  0  0  0  0  0  0  0999 V2000
   -1.7479    0.8366   -4.7851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734    0.7161   -3.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4888   -0.3163   -3.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0287   -0.6025   -1.6219 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0610   -1.1509   -1.4715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9733   -0.2634   -0.4697 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5984   -1.0374    0.7952 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2887   -0.1044    1.6143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3421    1.2520    0.8732 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5402    2.4325    1.8650 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6094    3.8002    1.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8257    2.2450    2.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9215    1.2259   -0.0505 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2070    1.5814    0.7338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7936    2.1711   -1.2698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7151    1.8480   -2.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4308   -0.0108   -5.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3513    1.7485   -5.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8417    0.8771   -4.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1415   -1.0427   -3.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9799   -0.5725   -0.7807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1008   -1.9920    0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5028   -1.2717    1.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1283   -0.0025    2.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2960   -0.5233    1.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2302    1.2229    0.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2965    2.4530    2.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3096    3.7930    0.3418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3721    4.1157    0.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    4.5739    1.8861 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7869    1.3375    3.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9735    3.0844    3.3773 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7053    2.1826    2.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3010    1.0049    1.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2300    2.6406    1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1040    1.3815    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2458    2.2042   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0292    3.1950   -0.9619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7434    1.6676   -2.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7506    2.7604   -3.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  6  1  0
 13  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
 13 15  1  0
  4  5  2  0
 16 15  1  0
  2  1  1  0
  6 13  1  0
  6 21  1  6
 13 14  1  1
  3  2  2  0
  9 10  1  0
  3  4  1  0
 10 11  1  0
  2 16  1  0
 10 12  1  0
  3 20  1  0
 16 39  1  0
 16 40  1  0
 15 37  1  0
 15 38  1  0
  9 26  1  6
  8 24  1  0
  8 25  1  0
  7 22  1  0
  7 23  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 10 27  1  1
 11 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O

Average Mass

220.3560 Da

Monoisotopic Mass

220.18272 Da

IUPAC Name

(1R,3aS,8aR)-6,8a-dimethyl-1-(propan-2-yl)-1,2,3,3a,4,7,8,8a-octahydroazulen-4-one

Traditional Name

(1R,3aS,8aR)-1-isopropyl-6,8a-dimethyl-1,2,3,3a,7,8-hexahydroazulen-4-one

CAS Registry Number

Not Available

SMILES

[H]C1=C(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@@]([H])(C1=O)C([H])([H])C([H])([H])[C@]2([H])C([H])(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C15H24O/c1-10(2)12-5-6-13-14(16)9-11(3)7-8-15(12,13)4/h9-10,12-13H,5-8H2,1-4H3/t12-,13-,15-/m1/s1

InChI Key

YJMPMKVSGMSRFT-UMVBOHGHSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Hortonia	JEOL database	Carr, G., et al, J. Nat. Prod. 75, 1189 (2012)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Ketones

Alternative Parents

Substituents

Ketone
Organic oxide
Hydrocarbon derivative
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	3.86	ALOGPS
logP	4.3	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	19.46	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	68.32 m³·mol⁻¹	ChemAxon
Polarizability	26.82 Å³	ChemAxon
Number of Rings	2	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

Not Available

Chemspider ID

28289846

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

60154791

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Carr, G., et al. (2012). Carr, G., et al, J. Nat. Prod. 75, 1189 (2012). J. Nat. Prod..

Showing NP-Card for hortonone A (NP0036811)

MOL for NP0036811 (hortonone A)

3D MOL for NP0036811 (hortonone A)

3D SDF for NP0036811 (hortonone A)

3D-SDF for NP0036811 (hortonone A)

PDB for NP0036811 (hortonone A)

3D PDB for NP0036811 (hortonone A)

SMILES for NP0036811 (hortonone A)

INCHI for NP0036811 (hortonone A)

Structure for NP0036811 (hortonone A)

3D Structure for NP0036811 (hortonone A)