NP-MRD: Showing NP-Card for (1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate (NP0154440)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 11:21:39 UTC

Updated at

2022-09-02 11:21:39 UTC

NP-MRD ID

NP0154440

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate

Description

(1S,3abeta,8aalpha)-1-Methyl-4-methylene-7beta-isopropyldecahydroazulene-1alpha,2beta,6alpha,8alpha-tetraol 2,6,8-triacetate belongs to the class of organic compounds known as guaianes. These are sesquiterpenoids with a structure based on the guaiane skeleton. Guaiane is a bicyclic compound consisting of a decahydroazulene moiety, substituted with two methyl groups and a 1-methylethyl group at the 1-, 4-, and 7-position, respectively. (1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate is found in Salvia roborowskii. Based on a literature review very few articles have been published on (1S,3abeta,8aalpha)-1-Methyl-4-methylene-7beta-isopropyldecahydroazulene-1alpha,2beta,6alpha,8alpha-tetraol 2,6,8-triacetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022213212D          

 28 29  0  0  1  0            999 V2000
    3.1690    1.5257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3526    0.7214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569    0.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5149   -0.2055    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3399   -0.2055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7524    0.5090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    1.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5774    0.5090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -0.9488    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6713   -1.5938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3699   -2.3618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4871   -1.4708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3526   -1.1324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1690   -1.9367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7738   -2.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5545   -2.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5902   -3.3021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076   -0.6180    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7076    0.2070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9230    0.4619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4380   -0.2055    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6130   -0.2055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2005    0.5090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6245    0.5090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6130    1.2235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230   -0.8729    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3157   -1.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0860   -1.6817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  1  0  0  0
  2 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
 18 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  6  0  0  0
M  END

     RDKit          3D

 60 61  0  0  0  0  0  0  0  0999 V2000
    0.5016    3.1826    1.4654 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3775    1.8784    1.3260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7434    1.2490    2.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8261    0.7380    1.1763 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0914    0.7372    1.7585 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1554    1.5222    1.3410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4668    1.4249    2.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9972    2.2895    0.3823 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3879   -0.5634    0.6060 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5088   -1.4360    0.1124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3323   -0.8236   -0.9646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3699   -1.8995    1.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3685   -0.2901   -0.4833 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4257   -1.2564   -1.5090 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7164   -0.9435   -2.8282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7782   -1.9576   -3.9127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9436    0.2496   -3.1544 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9461   -0.1717    0.1747 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3687    1.2640    0.4183 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7078    1.0398    1.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2692   -0.1528    0.2934 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3682    0.1755   -0.5009 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5841   -0.4709   -0.4048 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7168   -0.0764   -1.2777 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7229   -1.3908    0.4230 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1290   -0.6899   -0.5833 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2541   -0.1594   -1.9721 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0874   -2.0809   -0.5566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1806    3.7081    2.1089 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2730    3.7146    0.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2768    0.4402    2.6994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1975    1.9895    2.7670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8596    1.4847    0.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1626    0.8221    1.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9369    2.4394    2.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3701    0.9138    3.0203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9077   -1.1403    1.4529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0104   -2.3723   -0.2765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3747   -1.5186   -1.8268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9580    0.1654   -1.2896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3959   -0.7565   -0.6004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8993   -1.5585    2.2100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5207   -3.0021    1.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3487   -1.3657    1.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5990    0.7027   -0.9716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5201   -2.9706   -3.5713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1078   -1.6349   -4.7346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8202   -1.8972   -4.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9825   -0.6655    1.1873 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5053    1.8304   -0.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4014    1.8946    0.9387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5961    0.7389    2.1188 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5132   -0.9917    0.9975 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3603    0.2855   -2.2653 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2508    0.7588   -0.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4469   -0.9099   -1.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6025    0.6824   -2.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3152    0.2032   -2.1083 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1771   -1.0105   -2.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1002   -2.3677    0.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10 12  1  0
 10  9  1  0
  9  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 21 26  1  0
 26 27  1  0
 26 28  1  6
 26 18  1  0
 18 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
 13  9  1  0
 18 19  1  0
 11 39  1  0
 11 40  1  0
 11 41  1  0
 10 38  1  0
 12 42  1  0
 12 43  1  0
 12 44  1  0
  9 37  1  1
  4 33  1  6
  3 31  1  0
  3 32  1  0
  1 29  1  0
  1 30  1  0
 19 50  1  6
 20 51  1  0
 20 52  1  0
 21 53  1  1
 24 54  1  0
 24 55  1  0
 24 56  1  0
 27 57  1  0
 27 58  1  0
 27 59  1  0
 28 60  1  0
 18 49  1  1
 13 45  1  6
 16 46  1  0
 16 47  1  0
 16 48  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
M  END


  Mrv1652309022213212D          

 28 29  0  0  1  0            999 V2000
    3.1690    1.5257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3526    0.7214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569    0.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5149   -0.2055    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3399   -0.2055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7524    0.5090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    1.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5774    0.5090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -0.9488    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6713   -1.5938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3699   -2.3618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4871   -1.4708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3526   -1.1324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1690   -1.9367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7738   -2.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5545   -2.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5902   -3.3021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076   -0.6180    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7076    0.2070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9230    0.4619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4380   -0.2055    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6130   -0.2055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2005    0.5090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6245    0.5090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6130    1.2235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230   -0.8729    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3157   -1.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0860   -1.6817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  1  0  0  0
  2 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
 18 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0154440

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1[C@H](CC(=C)[C@H]2C[C@H](OC(C)=O)[C@@](C)(O)[C@@H]2[C@H]1OC(C)=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H32O7/c1-10(2)18-16(26-12(4)22)8-11(3)15-9-17(27-13(5)23)21(7,25)19(15)20(18)28-14(6)24/h10,15-20,25H,3,8-9H2,1-2,4-7H3/t15-,16+,17+,18-,19+,20+,21-/m1/s1

> <INCHI_KEY>
BUGLHVRUBMRPRP-SRWWVFQWSA-N

> <FORMULA>
C21H32O7

> <MOLECULAR_WEIGHT>
396.48

> <EXACT_MASS>
396.21480337

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
42.4758662549619

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3aS,6S,7R,8S,8aS)-6,8-bis(acetyloxy)-1-hydroxy-1-methyl-4-methylidene-7-(propan-2-yl)-decahydroazulen-2-yl acetate

> <ALOGPS_LOGP>
2.26

> <JCHEM_LOGP>
1.2327563783333333

> <ALOGPS_LOGS>
-3.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.707209395858307

> <JCHEM_PKA_STRONGEST_BASIC>
-3.364266610251576

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
100.23839999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.43e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3aS,6S,7R,8S,8aS)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       5.916   2.848   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.258   1.347   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.760   1.004   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.428  -0.384   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.968  -0.384   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.738   0.950   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.968   2.284   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      12.278   0.950   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.760  -1.771   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.720  -2.975   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.157  -4.409   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.243  -2.746   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.258  -2.114   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.916  -3.615   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.044  -4.663   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.502  -5.160   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.702  -6.164   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.054  -1.154   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.054   0.386   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.590   0.862   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.684  -0.384   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.144  -0.384   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.374   0.950   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.166   0.950   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.144   2.284   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.590  -1.629   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.456  -2.672   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.894  -3.139   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10   13                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    9   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   13   19   26                                                  
CONECT   19   18    2   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21   18   27   28                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Value	Source
(1S,3Abeta,8aalpha)-1-methyl-4-methylene-7b-isopropyldecahydroazulene-1a,2b,6a,8a-tetraol 2,6,8-triacetate	Generator
(1S,3Abeta,8aalpha)-1-methyl-4-methylene-7b-isopropyldecahydroazulene-1a,2b,6a,8a-tetraol 2,6,8-triacetic acid	Generator
(1S,3Abeta,8aalpha)-1-methyl-4-methylene-7beta-isopropyldecahydroazulene-1alpha,2beta,6alpha,8alpha-tetraol 2,6,8-triacetic acid	Generator
(1S,3Abeta,8aalpha)-1-methyl-4-methylene-7β-isopropyldecahydroazulene-1α,2β,6α,8α-tetraol 2,6,8-triacetate	Generator
(1S,3Abeta,8aalpha)-1-methyl-4-methylene-7β-isopropyldecahydroazulene-1α,2β,6α,8α-tetraol 2,6,8-triacetic acid	Generator

Chemical Formula

C₂₁H₃₂O₇

Average Mass

396.4800 Da

Monoisotopic Mass

396.21480 Da

IUPAC Name

(1S,2S,3aS,6S,7R,8S,8aS)-6,8-bis(acetyloxy)-1-hydroxy-1-methyl-4-methylidene-7-(propan-2-yl)-decahydroazulen-2-yl acetate

Traditional Name

(1S,2S,3aS,6S,7R,8S,8aS)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1[C@H](CC(=C)[C@H]2C[C@H](OC(C)=O)[C@@](C)(O)[C@@H]2[C@H]1OC(C)=O)OC(C)=O

InChI Identifier

InChI=1S/C21H32O7/c1-10(2)18-16(26-12(4)22)8-11(3)15-9-17(27-13(5)23)21(7,25)19(15)20(18)28-14(6)24/h10,15-20,25H,3,8-9H2,1-2,4-7H3/t15-,16+,17+,18-,19+,20+,21-/m1/s1

InChI Key

BUGLHVRUBMRPRP-SRWWVFQWSA-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
Salvia roborowskii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guaianes. These are sesquiterpenoids with a structure based on the guaiane skeleton. Guaiane is a bicyclic compound consisting of a decahydroazulene moiety, substituted with two methyl groups and a 1-methylethyl group at the 1-, 4-, and 7-position, respectively.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Guaianes

Alternative Parents

Substituents

Guaiane sesquiterpenoid
Tricarboxylic acid or derivatives
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	2.26	ALOGPS
logP	1.23	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	13.71	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	99.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	100.24 m³·mol⁻¹	ChemAxon
Polarizability	42.48 Å³	ChemAxon
Number of Rings	2	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

28286019

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102280052

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate (NP0154440)

MOL for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)

3D MOL for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)

3D SDF for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)

3D-SDF for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)

PDB for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)

3D PDB for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)

SMILES for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)

INCHI for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)

Structure for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)

3D Structure for NP0154440 ((1s,2s,3as,6s,7r,8s,8as)-6,8-bis(acetyloxy)-1-hydroxy-7-isopropyl-1-methyl-4-methylidene-octahydroazulen-2-yl acetate)