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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:41:13 UTC

Update Date

2022-03-07 02:52:50 UTC

HMDB ID

HMDB0031137

Secondary Accession Numbers

HMDB31137

Metabolite Identification

Common Name

Annosquamosin A

Description

Annosquamosin A belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Annosquamosin A is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 05061305452D          

 26 29  0  0  0  0            999 V2000
   -0.3996    4.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7828    2.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7366    0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3550    0.7609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1623    0.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9942    0.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7314    2.6342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6222    1.5413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5456    0.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9121    2.4782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0998    1.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7383    2.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7862    2.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3993    2.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6695    3.4229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5599    0.6390    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2704    2.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1836    1.0613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0798    2.1630    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0032    1.2235    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5715    1.6963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1409    1.3963    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7703    3.4139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4795    3.2668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5355    0.9239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1293    2.7993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  8  4  1  0  0  0  0
  9  4  1  0  0  0  0
 10  7  1  0  0  0  0
 15  1  1  0  0  0  0
 16  5  1  0  0  0  0
 16 11  1  1  0  0  0
 17  7  1  0  0  0  0
 18  6  1  0  0  0  0
 19  2  1  1  0  0  0
 19  8  1  0  0  0  0
 19 13  1  6  0  0  0
 19 17  1  0  0  0  0
 20  3  1  6  0  0  0
 20  9  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 10  1  0  0  0  0
 21 11  1  0  0  0  0
 21 12  1  0  0  0  0
 21 18  1  0  0  0  0
 22 12  1  0  0  0  0
 22 14  1  6  0  0  0
 22 16  1  0  0  0  0
 23 13  2  0  0  0  0
 24 15  2  0  0  0  0
 22 25  1  1  0  0  0
 26 14  1  0  0  0  0
 26 15  1  0  0  0  0
M  END

HMDB0031137
     RDKit          3D
Annosquamosin A
 60 63  0  0  0  0  0  0  0  0999 V2000
    6.8446    1.5397   -0.9003 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8615    0.5306   -0.3564 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9907    0.1163    0.8192 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8293    0.0506   -1.1073 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8308   -0.8580   -0.7909 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9248   -0.3773    0.2613 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5957   -0.1455    1.4462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7858   -1.3139    0.5806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5356   -0.4764    0.7545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2083   -0.8457    2.0205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4281    0.0673    2.0593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3782   -0.4602    1.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7556   -0.7597   -0.2991 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9847   -2.2521   -0.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4889   -0.0463   -1.4486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9512   -0.3563   -1.4236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5804   -0.1464   -0.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6168    0.4164    0.9351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3492    1.8661    0.7556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3004    0.2588    2.2715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0821    1.0472    3.1750 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3186   -0.4776   -0.4680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0227    0.8049   -1.2344 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4817    0.8821   -1.3736 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2037    0.9083   -0.0801 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1610    0.8971    1.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7755    1.4106   -0.3304 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9535    1.4564   -1.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4744    2.5834   -0.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2836   -1.8251   -0.3969 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3157   -1.1981   -1.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5832   -0.9854    1.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9820   -1.9772    1.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6479   -1.9634   -0.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5992   -1.8830    1.9671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4448   -0.6667    2.8780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8827   -0.0980    3.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1899    1.1216    1.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7814   -1.4145    1.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9680   -2.4435   -1.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1633   -2.8659   -0.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9220   -2.6034   -0.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3132    1.0267   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0756   -0.5448   -2.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4494    0.3298   -2.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1475   -1.3874   -1.8273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9006   -1.1489    0.3038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4678    0.5094   -0.1143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7575    2.5018    1.5985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3050    2.1660    0.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8825    2.2838   -0.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9979   -0.5425    2.4806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1172   -1.2689   -1.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4901    1.6938   -0.8357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4154    0.6462   -2.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6910    1.8607   -1.8977 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7842    0.1006   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9262    1.7282    0.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4621    1.7177    0.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6880    0.8104    2.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  1
 20 21  2  0
 13 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25  6  1  0
 22  9  1  0
 26  9  1  0
 18 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  5 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 14 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  0
 19 50  1  0
 19 51  1  0
 20 52  1  0
 22 53  1  0
 23 54  1  0
 23 55  1  0
 24 56  1  0
 24 57  1  0
 25 58  1  6
 26 59  1  0
 26 60  1  0
M  END


  Mrv0541 05061305452D          

 26 29  0  0  0  0            999 V2000
   -0.3996    4.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7828    2.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7366    0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3550    0.7609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1623    0.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9942    0.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7314    2.6342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6222    1.5413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5456    0.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9121    2.4782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0998    1.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7383    2.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7862    2.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3993    2.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6695    3.4229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5599    0.6390    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2704    2.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1836    1.0613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0798    2.1630    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0032    1.2235    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5715    1.6963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1409    1.3963    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7703    3.4139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4795    3.2668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5355    0.9239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1293    2.7993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  8  4  1  0  0  0  0
  9  4  1  0  0  0  0
 10  7  1  0  0  0  0
 15  1  1  0  0  0  0
 16  5  1  0  0  0  0
 16 11  1  1  0  0  0
 17  7  1  0  0  0  0
 18  6  1  0  0  0  0
 19  2  1  1  0  0  0
 19  8  1  0  0  0  0
 19 13  1  6  0  0  0
 19 17  1  0  0  0  0
 20  3  1  6  0  0  0
 20  9  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 10  1  0  0  0  0
 21 11  1  0  0  0  0
 21 12  1  0  0  0  0
 21 18  1  0  0  0  0
 22 12  1  0  0  0  0
 22 14  1  6  0  0  0
 22 16  1  0  0  0  0
 23 13  2  0  0  0  0
 24 15  2  0  0  0  0
 22 25  1  1  0  0  0
 26 14  1  0  0  0  0
 26 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0031137

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(=O)OC[C@]1(O)CC23C[C@@H]1CCC2[C@]1(C)CCC[C@@](C)(C=O)C1CC3

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O4/c1-15(24)26-14-22(25)12-21-10-7-17-19(2,13-23)8-4-9-20(17,3)18(21)6-5-16(22)11-21/h13,16-18,25H,4-12,14H2,1-3H3/t16-,17?,18?,19-,20+,21?,22+/m0/s1

> <INCHI_KEY>
FCHGRGOUMXZTFS-QZRFJHGNSA-N

> <FORMULA>
C22H34O4

> <MOLECULAR_WEIGHT>
362.503

> <EXACT_MASS>
362.245709576

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
41.15301052695048

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(5R,9S,13S,14S)-5-formyl-14-hydroxy-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]methyl acetate

> <ALOGPS_LOGP>
3.11

> <JCHEM_LOGP>
3.0758685416666687

> <ALOGPS_LOGS>
-4.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.752230213691345

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3445745045314057

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
99.03799999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.89e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(5R,9S,13S,14S)-5-formyl-14-hydroxy-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0031137
     RDKit          3D
Annosquamosin A
 60 63  0  0  0  0  0  0  0  0999 V2000
    6.8446    1.5397   -0.9003 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8615    0.5306   -0.3564 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9907    0.1163    0.8192 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8293    0.0506   -1.1073 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8308   -0.8580   -0.7909 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9248   -0.3773    0.2613 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5957   -0.1455    1.4462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7858   -1.3139    0.5806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5356   -0.4764    0.7545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2083   -0.8457    2.0205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4281    0.0673    2.0593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3782   -0.4602    1.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7556   -0.7597   -0.2991 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9847   -2.2521   -0.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4889   -0.0463   -1.4486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9512   -0.3563   -1.4236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5804   -0.1464   -0.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6168    0.4164    0.9351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3492    1.8661    0.7556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3004    0.2588    2.2715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0821    1.0472    3.1750 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3186   -0.4776   -0.4680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0227    0.8049   -1.2344 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4817    0.8821   -1.3736 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2037    0.9083   -0.0801 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1610    0.8971    1.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7755    1.4106   -0.3304 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9535    1.4564   -1.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4744    2.5834   -0.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2836   -1.8251   -0.3969 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3157   -1.1981   -1.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5832   -0.9854    1.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9820   -1.9772    1.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6479   -1.9634   -0.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5992   -1.8830    1.9671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4448   -0.6667    2.8780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8827   -0.0980    3.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1899    1.1216    1.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7814   -1.4145    1.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9680   -2.4435   -1.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1633   -2.8659   -0.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9220   -2.6034   -0.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3132    1.0267   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0756   -0.5448   -2.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4494    0.3298   -2.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1475   -1.3874   -1.8273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9006   -1.1489    0.3038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4678    0.5094   -0.1143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7575    2.5018    1.5985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3050    2.1660    0.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8825    2.2838   -0.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9979   -0.5425    2.4806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1172   -1.2689   -1.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4901    1.6938   -0.8357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4154    0.6462   -2.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6910    1.8607   -1.8977 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7842    0.1006   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9262    1.7282    0.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4621    1.7177    0.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6880    0.8104    2.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  1
 20 21  2  0
 13 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25  6  1  0
 22  9  1  0
 26  9  1  0
 18 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  5 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 14 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  0
 19 50  1  0
 19 51  1  0
 20 52  1  0
 22 53  1  0
 23 54  1  0
 23 55  1  0
 24 56  1  0
 24 57  1  0
 25 58  1  6
 26 59  1  0
 26 60  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -0.746   7.845   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.061   5.474   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.108   0.827   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.129   1.420   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.170   0.028   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.722   0.398   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.099   4.917   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.628   2.877   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.618   1.124   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.569   4.626   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.053   2.140   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.378   3.797   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.934   4.833   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.745   3.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.250   6.389   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.045   1.193   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.105   3.741   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.076   1.981   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.616   4.038   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.606   2.284   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.933   3.166   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.263   2.606   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.905   6.373   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -2.762   6.098   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -1.000   1.725   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -0.241   5.225   0.000  0.00  0.00           O+0
CONECT    1   15                                                            
CONECT    2   19                                                            
CONECT    3   20                                                            
CONECT    4    8    9                                                       
CONECT    5    6   16                                                       
CONECT    6    5   18                                                       
CONECT    7   10   17                                                       
CONECT    8    4   19                                                       
CONECT    9    4   20                                                       
CONECT   10    7   21                                                       
CONECT   11   16   21                                                       
CONECT   12   21   22                                                       
CONECT   13   19   23                                                       
CONECT   14   22   26                                                       
CONECT   15    1   24   26                                                  
CONECT   16    5   11   22                                                  
CONECT   17    7   19   20                                                  
CONECT   18    6   20   21                                                  
CONECT   19    2    8   13   17                                             
CONECT   20    3    9   17   18                                             
CONECT   21   10   11   12   18                                             
CONECT   22   12   14   16   25                                             
CONECT   23   13                                                            
CONECT   24   15                                                            
CONECT   25   22                                                            
CONECT   26   14   15                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

COMPND    HMDB0031137
HETATM    1  C1  UNL     1       6.845   1.540  -0.900  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.862   0.531  -0.356  1.00  0.00           C  
HETATM    3  O1  UNL     1       5.991   0.116   0.819  1.00  0.00           O  
HETATM    4  O2  UNL     1       4.829   0.051  -1.107  1.00  0.00           O  
HETATM    5  C3  UNL     1       3.831  -0.858  -0.791  1.00  0.00           C  
HETATM    6  C4  UNL     1       2.925  -0.377   0.261  1.00  0.00           C  
HETATM    7  O3  UNL     1       3.596  -0.145   1.446  1.00  0.00           O  
HETATM    8  C5  UNL     1       1.786  -1.314   0.581  1.00  0.00           C  
HETATM    9  C6  UNL     1       0.536  -0.476   0.754  1.00  0.00           C  
HETATM   10  C7  UNL     1      -0.208  -0.846   2.021  1.00  0.00           C  
HETATM   11  C8  UNL     1      -1.428   0.067   2.059  1.00  0.00           C  
HETATM   12  C9  UNL     1      -2.378  -0.460   1.012  1.00  0.00           C  
HETATM   13  C10 UNL     1      -1.756  -0.760  -0.299  1.00  0.00           C  
HETATM   14  C11 UNL     1      -1.985  -2.252  -0.609  1.00  0.00           C  
HETATM   15  C12 UNL     1      -2.489  -0.046  -1.449  1.00  0.00           C  
HETATM   16  C13 UNL     1      -3.951  -0.356  -1.424  1.00  0.00           C  
HETATM   17  C14 UNL     1      -4.580  -0.146  -0.086  1.00  0.00           C  
HETATM   18  C15 UNL     1      -3.617   0.416   0.935  1.00  0.00           C  
HETATM   19  C16 UNL     1      -3.349   1.866   0.756  1.00  0.00           C  
HETATM   20  C17 UNL     1      -4.300   0.259   2.272  1.00  0.00           C  
HETATM   21  O4  UNL     1      -4.082   1.047   3.175  1.00  0.00           O  
HETATM   22  C18 UNL     1      -0.319  -0.478  -0.468  1.00  0.00           C  
HETATM   23  C19 UNL     1      -0.023   0.805  -1.234  1.00  0.00           C  
HETATM   24  C20 UNL     1       1.482   0.882  -1.374  1.00  0.00           C  
HETATM   25  C21 UNL     1       2.204   0.908  -0.080  1.00  0.00           C  
HETATM   26  C22 UNL     1       1.161   0.897   1.036  1.00  0.00           C  
HETATM   27  H1  UNL     1       7.775   1.411  -0.330  1.00  0.00           H  
HETATM   28  H2  UNL     1       6.953   1.456  -1.987  1.00  0.00           H  
HETATM   29  H3  UNL     1       6.474   2.583  -0.697  1.00  0.00           H  
HETATM   30  H4  UNL     1       4.284  -1.825  -0.397  1.00  0.00           H  
HETATM   31  H5  UNL     1       3.316  -1.198  -1.721  1.00  0.00           H  
HETATM   32  H6  UNL     1       3.583  -0.985   1.961  1.00  0.00           H  
HETATM   33  H7  UNL     1       1.982  -1.977   1.427  1.00  0.00           H  
HETATM   34  H8  UNL     1       1.648  -1.963  -0.320  1.00  0.00           H  
HETATM   35  H9  UNL     1      -0.599  -1.883   1.967  1.00  0.00           H  
HETATM   36  H10 UNL     1       0.445  -0.667   2.878  1.00  0.00           H  
HETATM   37  H11 UNL     1      -1.883  -0.098   3.074  1.00  0.00           H  
HETATM   38  H12 UNL     1      -1.190   1.122   1.992  1.00  0.00           H  
HETATM   39  H13 UNL     1      -2.781  -1.415   1.481  1.00  0.00           H  
HETATM   40  H14 UNL     1      -1.968  -2.444  -1.690  1.00  0.00           H  
HETATM   41  H15 UNL     1      -1.163  -2.866  -0.166  1.00  0.00           H  
HETATM   42  H16 UNL     1      -2.922  -2.603  -0.145  1.00  0.00           H  
HETATM   43  H17 UNL     1      -2.313   1.027  -1.456  1.00  0.00           H  
HETATM   44  H18 UNL     1      -2.076  -0.545  -2.376  1.00  0.00           H  
HETATM   45  H19 UNL     1      -4.449   0.330  -2.142  1.00  0.00           H  
HETATM   46  H20 UNL     1      -4.148  -1.387  -1.827  1.00  0.00           H  
HETATM   47  H21 UNL     1      -4.901  -1.149   0.304  1.00  0.00           H  
HETATM   48  H22 UNL     1      -5.468   0.509  -0.114  1.00  0.00           H  
HETATM   49  H23 UNL     1      -3.757   2.502   1.599  1.00  0.00           H  
HETATM   50  H24 UNL     1      -2.305   2.166   0.652  1.00  0.00           H  
HETATM   51  H25 UNL     1      -3.883   2.284  -0.150  1.00  0.00           H  
HETATM   52  H26 UNL     1      -4.998  -0.542   2.481  1.00  0.00           H  
HETATM   53  H27 UNL     1       0.117  -1.269  -1.155  1.00  0.00           H  
HETATM   54  H28 UNL     1      -0.490   1.694  -0.836  1.00  0.00           H  
HETATM   55  H29 UNL     1      -0.415   0.646  -2.279  1.00  0.00           H  
HETATM   56  H30 UNL     1       1.691   1.861  -1.898  1.00  0.00           H  
HETATM   57  H31 UNL     1       1.784   0.101  -2.078  1.00  0.00           H  
HETATM   58  H32 UNL     1       2.926   1.728   0.039  1.00  0.00           H  
HETATM   59  H33 UNL     1       0.462   1.718   0.962  1.00  0.00           H  
HETATM   60  H34 UNL     1       1.688   0.810   2.005  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3    3    4
CONECT    4    5
CONECT    5    6   30   31
CONECT    6    7    8   25
CONECT    7   32
CONECT    8    9   33   34
CONECT    9   10   22   26
CONECT   10   11   35   36
CONECT   11   12   37   38
CONECT   12   13   18   39
CONECT   13   14   15   22
CONECT   14   40   41   42
CONECT   15   16   43   44
CONECT   16   17   45   46
CONECT   17   18   47   48
CONECT   18   19   20
CONECT   19   49   50   51
CONECT   20   21   21   52
CONECT   22   23   53
CONECT   23   24   54   55
CONECT   24   25   56   57
CONECT   25   26   58
CONECT   26   59   60
END

HMDB0031137
     RDKit          3D
Annosquamosin A
 60 63  0  0  0  0  0  0  0  0999 V2000
    6.8446    1.5397   -0.9003 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8615    0.5306   -0.3564 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9907    0.1163    0.8192 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8293    0.0506   -1.1073 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8308   -0.8580   -0.7909 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9248   -0.3773    0.2613 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5957   -0.1455    1.4462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7858   -1.3139    0.5806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5356   -0.4764    0.7545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2083   -0.8457    2.0205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4281    0.0673    2.0593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3782   -0.4602    1.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7556   -0.7597   -0.2991 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9847   -2.2521   -0.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4889   -0.0463   -1.4486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9512   -0.3563   -1.4236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5804   -0.1464   -0.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6168    0.4164    0.9351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3492    1.8661    0.7556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3004    0.2588    2.2715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0821    1.0472    3.1750 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3186   -0.4776   -0.4680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0227    0.8049   -1.2344 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4817    0.8821   -1.3736 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2037    0.9083   -0.0801 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1610    0.8971    1.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7755    1.4106   -0.3304 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9535    1.4564   -1.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4744    2.5834   -0.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2836   -1.8251   -0.3969 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3157   -1.1981   -1.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5832   -0.9854    1.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9820   -1.9772    1.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6479   -1.9634   -0.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5992   -1.8830    1.9671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4448   -0.6667    2.8780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8827   -0.0980    3.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1899    1.1216    1.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7814   -1.4145    1.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9680   -2.4435   -1.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1633   -2.8659   -0.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9220   -2.6034   -0.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3132    1.0267   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0756   -0.5448   -2.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4494    0.3298   -2.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1475   -1.3874   -1.8273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9006   -1.1489    0.3038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4678    0.5094   -0.1143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7575    2.5018    1.5985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3050    2.1660    0.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8825    2.2838   -0.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9979   -0.5425    2.4806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1172   -1.2689   -1.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4901    1.6938   -0.8357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4154    0.6462   -2.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6910    1.8607   -1.8977 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7842    0.1006   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9262    1.7282    0.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4621    1.7177    0.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6880    0.8104    2.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  1
 20 21  2  0
 13 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25  6  1  0
 22  9  1  0
 26  9  1  0
 18 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  5 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 14 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  0
 19 50  1  0
 19 51  1  0
 20 52  1  0
 22 53  1  0
 23 54  1  0
 23 55  1  0
 24 56  1  0
 24 57  1  0
 25 58  1  6
 26 59  1  0
 26 60  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
[(5R,9S,13S,14S)-5-Formyl-14-hydroxy-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]methyl acetic acid	Generator
16beta-Hydroxy-17-acetoxy-ent-kauran-19-al	MeSH
Annosquamosin a	MeSH

Chemical Formula

C₂₂H₃₄O₄

Average Molecular Weight

362.503

Monoisotopic Molecular Weight

362.245709576

IUPAC Name

[(5R,9S,13S,14S)-5-formyl-14-hydroxy-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]methyl acetate

Traditional Name

[(5R,9S,13S,14S)-5-formyl-14-hydroxy-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]methyl acetate

CAS Registry Number

192584-48-8

SMILES

CC(=O)OC[C@]1(O)CC23C[C@@H]1CCC2[C@]1(C)CCC[C@@](C)(C=O)C1CC3

InChI Identifier

InChI=1S/C22H34O4/c1-15(24)26-14-22(25)12-21-10-7-17-19(2,13-23)8-4-9-20(17,3)18(21)6-5-16(22)11-21/h13,16-18,25H,4-12,14H2,1-3H3/t16-,17?,18?,19-,20+,21?,22+/m0/s1

InChI Key

FCHGRGOUMXZTFS-QZRFJHGNSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0031137)
Cell membrane (HMDB: HMDB0031137)

Cellular substructure

Extracellular (HMDB: HMDB0031137)
Membrane (HMDB: HMDB0031137)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0031137)

Source

Endogenous

Endogenous (HMDB: HMDB0031137)

Plant

Plant (HMDB: HMDB0031137)

Animal

Animal (HMDB: HMDB0031137)

Exogenous

Food

Food (HMDB: HMDB0031137)

Fruit

Fruits (FooDB: FOOD00871)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0031137)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0031137)

Cellular process

Cell signaling (HMDB: HMDB0031137)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0031137)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0031137)

Nutrient

Nutrient (HMDB: HMDB0031137)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0031137)

Emulsifier (HMDB: HMDB0031137)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	215 - 216 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0039 g/L	ALOGPS
logP	3.11	ALOGPS
logP	3.08	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	13.75	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	99.04 m³·mol⁻¹	ChemAxon
Polarizability	41.15 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	183.492	31661259
DarkChem	[M-H]-	181.277	31661259
DeepCCS	[M-2H]-	212.949	30932474
DeepCCS	[M+Na]+	187.756	30932474
AllCCS	[M+H]+	190.2	32859911
AllCCS	[M+H-H2O]+	187.8	32859911
AllCCS	[M+NH4]+	192.4	32859911
AllCCS	[M+Na]+	193.0	32859911
AllCCS	[M-H]-	190.9	32859911
AllCCS	[M+Na-2H]-	191.6	32859911
AllCCS	[M+HCOO]-	192.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Annosquamosin A	CC(=O)OC[C@]1(O)CC23C[C@@H]1CCC2[C@]1(C)CCC[C@@](C)(C=O)C1CC3	3033.0	Standard polar	33892256
Annosquamosin A	CC(=O)OC[C@]1(O)CC23C[C@@H]1CCC2[C@]1(C)CCC[C@@](C)(C=O)C1CC3	2623.2	Standard non polar	33892256
Annosquamosin A	CC(=O)OC[C@]1(O)CC23C[C@@H]1CCC2[C@]1(C)CCC[C@@](C)(C=O)C1CC3	2841.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Annosquamosin A,1TMS,isomer #1	CC(=O)OC[C@]1(O[Si](C)(C)C)CC23CCC4[C@@](C)(CCC[C@@]4(C)C=O)C2CC[C@H]1C3	2852.7	Semi standard non polar	33892256
Annosquamosin A,1TBDMS,isomer #1	CC(=O)OC[C@]1(O[Si](C)(C)C(C)(C)C)CC23CCC4[C@@](C)(CCC[C@@]4(C)C=O)C2CC[C@H]1C3	3117.0	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Annosquamosin A GC-MS (Non-derivatized) - 70eV, Positive	splash10-0002-2093000000-f88d4e65f5821a536dde	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Annosquamosin A GC-MS (1 TMS) - 70eV, Positive	splash10-05vy-9246600000-bcafd0d01386dd9c0a6e	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Annosquamosin A GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 10V, Negative-QTOF	splash10-03di-5009000000-f694ccd31c80b6c3387a	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 20V, Negative-QTOF	splash10-0bt9-9017000000-da811a527664ad79d2ee	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 40V, Negative-QTOF	splash10-0a4l-9021000000-08698cf77f3208553947	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 10V, Negative-QTOF	splash10-03di-0009000000-64c7eccecc0e967c403c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 20V, Negative-QTOF	splash10-03di-0029000000-9a68be9e7af1b9aa936e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 40V, Negative-QTOF	splash10-0079-2090000000-8ac52bcc9d493686ae93	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 10V, Positive-QTOF	splash10-0ik9-0009000000-b83cf2b4d3f5238ee709	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 20V, Positive-QTOF	splash10-0udi-1239000000-b68c3d758392bbf1d758	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 40V, Positive-QTOF	splash10-03dl-5491000000-67f8d4f377e0ee29eaee	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 10V, Positive-QTOF	splash10-01q9-0049000000-15a296bfd2bde7abc4c9	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 20V, Positive-QTOF	splash10-02mi-0594000000-8cf01656333229e29aea	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Annosquamosin A 40V, Positive-QTOF	splash10-01w1-0921000000-36ca0c7950a7b831bfac	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB003148

KNApSAcK ID

Not Available

Chemspider ID

412204

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

469215

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Annosquamosin A (HMDB0031137)

MOL for HMDB0031137 (Annosquamosin A)

3D MOL for HMDB0031137 (Annosquamosin A)

3D SDF for HMDB0031137 (Annosquamosin A)

3D-SDF for HMDB0031137 (Annosquamosin A)

PDB for HMDB0031137 (Annosquamosin A)

3D PDB for HMDB0031137 (Annosquamosin A)

SMILES for HMDB0031137 (Annosquamosin A)

INCHI for HMDB0031137 (Annosquamosin A)

Structure for HMDB0031137 (Annosquamosin A)

3D Structure for HMDB0031137 (Annosquamosin A)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra