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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 01:15:04 UTC

Update Date

2022-03-07 02:56:19 UTC

HMDB ID

HMDB0039716

Secondary Accession Numbers

HMDB39716

Metabolite Identification

Common Name

12alpha-12-Hydroxy-7,13-abietadien-18-oic acid

Description

12alpha-12-Hydroxy-7,13-abietadien-18-oic acid belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Based on a literature review a small amount of articles have been published on 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid.

Structure

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

HMDB0039716
     RDKit          3D
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid
 53 55  0  0  0  0  0  0  0  0999 V2000
    4.9924    1.4820    0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3976    0.3506    0.0504 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9103   -0.9395    0.6203 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9354    0.4328    0.1516 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.5564    0.6920 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8044   -0.4689    0.7890 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1101   -1.2226    1.6273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3654   -1.0182    1.6118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9494   -1.0421    0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3453   -0.5735    0.2800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2985   -1.7599    0.4083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6387    0.3060    1.4410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4132   -0.0025    2.3759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0277    1.5481    1.5123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8296    0.1976   -0.9243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7614    1.0963   -1.4947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6509    0.2153   -1.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0186   -0.4337   -0.7565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1237   -1.5315   -1.3847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0084    0.4675   -0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9156    1.1569   -1.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1936    1.6149   -0.3409 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9839    2.2546   -1.2890 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1058    1.3168    0.9514 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7853    2.4138    0.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5342    1.4474    1.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7343    0.4075   -1.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7684   -1.0417    1.7054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5334   -1.8241    0.0596 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0247   -0.9448    0.4514 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7475   -1.4462    1.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6106   -1.9399    2.2769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508   -0.0952    2.1633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8575   -1.8306    2.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9742   -2.1573   -0.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2272   -2.2287    1.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9612   -2.5239   -0.3248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3367   -1.4592    0.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5334    2.4274    1.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1594   -0.4745   -1.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6940    0.8466   -0.6774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2044    1.5732   -2.4037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4704    1.9081   -0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0794   -0.5853   -2.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9379    0.7869   -2.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2914   -1.2143   -2.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530   -1.8550   -0.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7630   -2.4372   -1.5970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4779    1.2319    0.5876 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4266    2.0813   -1.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1973    0.5549   -1.8762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9880    2.2570    0.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7608    3.2316   -1.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 12 14  1  0
 10 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22  4  1  0
 20  6  1  0
 18  9  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 21 50  1  0
 21 51  1  0
 22 52  1  0
 23 53  1  0
M  END


  Mrv0541 05061311212D          

 23 25  0  0  0  0            999 V2000
    7.3954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5886    0.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6701    0.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0382   -0.3587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5269    0.9841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  8  5  1  0  0  0  0
  9  5  1  0  0  0  0
 12  1  1  0  0  0  0
 12  2  1  0  0  0  0
 13  6  2  0  0  0  0
 13 10  1  0  0  0  0
 14 10  2  0  0  0  0
 14 12  1  0  0  0  0
 15 11  1  0  0  0  0
 15 13  1  0  0  0  0
 16 11  1  0  0  0  0
 16 14  1  0  0  0  0
 17  7  1  0  0  0  0
 19  3  1  0  0  0  0
 19  8  1  0  0  0  0
 19 15  1  0  0  0  0
 19 17  1  0  0  0  0
 20  4  1  0  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 16  1  0  0  0  0
 22 18  2  0  0  0  0
 23 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0039716

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C1=CC2=CCC3C(C)(CCCC3(C)C(O)=O)C2CC1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O3/c1-12(2)14-10-13-6-7-17-19(3,15(13)11-16(14)21)8-5-9-20(17,4)18(22)23/h6,10,12,15-17,21H,5,7-9,11H2,1-4H3,(H,22,23)

> <INCHI_KEY>
DYNISIGUMYFVJW-UHFFFAOYSA-N

> <FORMULA>
C20H30O3

> <MOLECULAR_WEIGHT>
318.4504

> <EXACT_MASS>
318.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
37.0603161940235

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-hydroxy-1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,4b,5,6,10,10a-decahydrophenanthrene-1-carboxylic acid

> <ALOGPS_LOGP>
4.31

> <JCHEM_LOGP>
3.721753993333334

> <ALOGPS_LOGS>
-3.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.835616567327794

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.467012438036324

> <JCHEM_PKA_STRONGEST_BASIC>
-1.121102527477552

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
92.72969999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.96e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxy-7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0039716
     RDKit          3D
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid
 53 55  0  0  0  0  0  0  0  0999 V2000
    4.9924    1.4820    0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3976    0.3506    0.0504 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9103   -0.9395    0.6203 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9354    0.4328    0.1516 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.5564    0.6920 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8044   -0.4689    0.7890 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1101   -1.2226    1.6273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3654   -1.0182    1.6118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9494   -1.0421    0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3453   -0.5735    0.2800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2985   -1.7599    0.4083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6387    0.3060    1.4410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4132   -0.0025    2.3759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0277    1.5481    1.5123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8296    0.1976   -0.9243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7614    1.0963   -1.4947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6509    0.2153   -1.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0186   -0.4337   -0.7565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1237   -1.5315   -1.3847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0084    0.4675   -0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9156    1.1569   -1.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1936    1.6149   -0.3409 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9839    2.2546   -1.2890 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1058    1.3168    0.9514 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7853    2.4138    0.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5342    1.4474    1.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7343    0.4075   -1.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7684   -1.0417    1.7054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5334   -1.8241    0.0596 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0247   -0.9448    0.4514 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7475   -1.4462    1.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6106   -1.9399    2.2769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508   -0.0952    2.1633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8575   -1.8306    2.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9742   -2.1573   -0.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2272   -2.2287    1.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9612   -2.5239   -0.3248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3367   -1.4592    0.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5334    2.4274    1.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1594   -0.4745   -1.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6940    0.8466   -0.6774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2044    1.5732   -2.4037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4704    1.9081   -0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0794   -0.5853   -2.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9379    0.7869   -2.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2914   -1.2143   -2.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530   -1.8550   -0.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7630   -2.4372   -1.5970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4779    1.2319    0.5876 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4266    2.0813   -1.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1973    0.5549   -1.8762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9880    2.2570    0.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7608    3.2316   -1.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 12 14  1  0
 10 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22  4  1  0
 20  6  1  0
 18  9  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 21 50  1  0
 21 51  1  0
 22 52  1  0
 23 53  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      13.805  -2.874   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.805  -0.206   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.645  -2.874   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.832   1.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.035  -1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.118   0.320   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.495  -4.207   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       1.938  -0.670   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.850   1.837   0.000  0.00  0.00           O+0
CONECT    1   12                                                            
CONECT    2   12                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5    8    9                                                       
CONECT    6    7   13                                                       
CONECT    7    6   17                                                       
CONECT    8    5   19                                                       
CONECT    9    5   20                                                       
CONECT   10   13   14                                                       
CONECT   11   15   16                                                       
CONECT   12    1    2   14                                                  
CONECT   13    6   10   15                                                  
CONECT   14   10   12   16                                                  
CONECT   15   11   13   19                                                  
CONECT   16   11   14   21                                                  
CONECT   17    7   19   20                                                  
CONECT   18   20   22   23                                                  
CONECT   19    3    8   15   17                                             
CONECT   20    4    9   17   18                                             
CONECT   21   16                                                            
CONECT   22   18                                                            
CONECT   23   18                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

COMPND    HMDB0039716
HETATM    1  C1  UNL     1       4.992   1.482   0.873  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.398   0.351   0.050  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.910  -0.940   0.620  1.00  0.00           C  
HETATM    4  C4  UNL     1       2.935   0.433   0.152  1.00  0.00           C  
HETATM    5  C5  UNL     1       2.253  -0.556   0.692  1.00  0.00           C  
HETATM    6  C6  UNL     1       0.804  -0.469   0.789  1.00  0.00           C  
HETATM    7  C7  UNL     1       0.110  -1.223   1.627  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.365  -1.018   1.612  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.949  -1.042   0.212  1.00  0.00           C  
HETATM   10  C10 UNL     1      -3.345  -0.573   0.280  1.00  0.00           C  
HETATM   11  C11 UNL     1      -4.299  -1.760   0.408  1.00  0.00           C  
HETATM   12  C12 UNL     1      -3.639   0.306   1.441  1.00  0.00           C  
HETATM   13  O1  UNL     1      -4.413  -0.002   2.376  1.00  0.00           O  
HETATM   14  O2  UNL     1      -3.028   1.548   1.512  1.00  0.00           O  
HETATM   15  C13 UNL     1      -3.830   0.198  -0.924  1.00  0.00           C  
HETATM   16  C14 UNL     1      -2.761   1.096  -1.495  1.00  0.00           C  
HETATM   17  C15 UNL     1      -1.651   0.215  -1.939  1.00  0.00           C  
HETATM   18  C16 UNL     1      -1.019  -0.434  -0.756  1.00  0.00           C  
HETATM   19  C17 UNL     1      -0.124  -1.531  -1.385  1.00  0.00           C  
HETATM   20  C18 UNL     1      -0.008   0.467  -0.048  1.00  0.00           C  
HETATM   21  C19 UNL     1       0.916   1.157  -1.009  1.00  0.00           C  
HETATM   22  C20 UNL     1       2.194   1.615  -0.341  1.00  0.00           C  
HETATM   23  O3  UNL     1       2.984   2.255  -1.289  1.00  0.00           O  
HETATM   24  H1  UNL     1       6.106   1.317   0.951  1.00  0.00           H  
HETATM   25  H2  UNL     1       4.785   2.414   0.306  1.00  0.00           H  
HETATM   26  H3  UNL     1       4.534   1.447   1.865  1.00  0.00           H  
HETATM   27  H4  UNL     1       4.734   0.407  -1.005  1.00  0.00           H  
HETATM   28  H5  UNL     1       4.768  -1.042   1.705  1.00  0.00           H  
HETATM   29  H6  UNL     1       4.533  -1.824   0.060  1.00  0.00           H  
HETATM   30  H7  UNL     1       6.025  -0.945   0.451  1.00  0.00           H  
HETATM   31  H8  UNL     1       2.748  -1.446   1.072  1.00  0.00           H  
HETATM   32  H9  UNL     1       0.611  -1.940   2.277  1.00  0.00           H  
HETATM   33  H10 UNL     1      -1.551  -0.095   2.163  1.00  0.00           H  
HETATM   34  H11 UNL     1      -1.858  -1.831   2.213  1.00  0.00           H  
HETATM   35  H12 UNL     1      -1.974  -2.157  -0.023  1.00  0.00           H  
HETATM   36  H13 UNL     1      -4.227  -2.229   1.407  1.00  0.00           H  
HETATM   37  H14 UNL     1      -3.961  -2.524  -0.325  1.00  0.00           H  
HETATM   38  H15 UNL     1      -5.337  -1.459   0.174  1.00  0.00           H  
HETATM   39  H16 UNL     1      -3.533   2.427   1.554  1.00  0.00           H  
HETATM   40  H17 UNL     1      -4.159  -0.474  -1.742  1.00  0.00           H  
HETATM   41  H18 UNL     1      -4.694   0.847  -0.677  1.00  0.00           H  
HETATM   42  H19 UNL     1      -3.204   1.573  -2.404  1.00  0.00           H  
HETATM   43  H20 UNL     1      -2.470   1.908  -0.820  1.00  0.00           H  
HETATM   44  H21 UNL     1      -2.079  -0.585  -2.578  1.00  0.00           H  
HETATM   45  H22 UNL     1      -0.938   0.787  -2.540  1.00  0.00           H  
HETATM   46  H23 UNL     1       0.291  -1.214  -2.336  1.00  0.00           H  
HETATM   47  H24 UNL     1       0.653  -1.855  -0.693  1.00  0.00           H  
HETATM   48  H25 UNL     1      -0.763  -2.437  -1.597  1.00  0.00           H  
HETATM   49  H26 UNL     1      -0.478   1.232   0.588  1.00  0.00           H  
HETATM   50  H27 UNL     1       0.427   2.081  -1.406  1.00  0.00           H  
HETATM   51  H28 UNL     1       1.197   0.555  -1.876  1.00  0.00           H  
HETATM   52  H29 UNL     1       1.988   2.257   0.538  1.00  0.00           H  
HETATM   53  H30 UNL     1       2.761   3.232  -1.265  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3    4   27
CONECT    3   28   29   30
CONECT    4    5    5   22
CONECT    5    6   31
CONECT    6    7    7   20
CONECT    7    8   32
CONECT    8    9   33   34
CONECT    9   10   18   35
CONECT   10   11   12   15
CONECT   11   36   37   38
CONECT   12   13   13   14
CONECT   14   39
CONECT   15   16   40   41
CONECT   16   17   42   43
CONECT   17   18   44   45
CONECT   18   19   20
CONECT   19   46   47   48
CONECT   20   21   49
CONECT   21   22   50   51
CONECT   22   23   52
CONECT   23   53
END

HMDB0039716
     RDKit          3D
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid
 53 55  0  0  0  0  0  0  0  0999 V2000
    4.9924    1.4820    0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3976    0.3506    0.0504 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9103   -0.9395    0.6203 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9354    0.4328    0.1516 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.5564    0.6920 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8044   -0.4689    0.7890 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1101   -1.2226    1.6273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3654   -1.0182    1.6118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9494   -1.0421    0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3453   -0.5735    0.2800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2985   -1.7599    0.4083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6387    0.3060    1.4410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4132   -0.0025    2.3759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0277    1.5481    1.5123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8296    0.1976   -0.9243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7614    1.0963   -1.4947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6509    0.2153   -1.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0186   -0.4337   -0.7565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1237   -1.5315   -1.3847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0084    0.4675   -0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9156    1.1569   -1.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1936    1.6149   -0.3409 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9839    2.2546   -1.2890 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1058    1.3168    0.9514 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7853    2.4138    0.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5342    1.4474    1.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7343    0.4075   -1.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7684   -1.0417    1.7054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5334   -1.8241    0.0596 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0247   -0.9448    0.4514 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7475   -1.4462    1.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6106   -1.9399    2.2769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508   -0.0952    2.1633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8575   -1.8306    2.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9742   -2.1573   -0.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2272   -2.2287    1.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9612   -2.5239   -0.3248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3367   -1.4592    0.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5334    2.4274    1.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1594   -0.4745   -1.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6940    0.8466   -0.6774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2044    1.5732   -2.4037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4704    1.9081   -0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0794   -0.5853   -2.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9379    0.7869   -2.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2914   -1.2143   -2.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530   -1.8550   -0.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7630   -2.4372   -1.5970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4779    1.2319    0.5876 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4266    2.0813   -1.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1973    0.5549   -1.8762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9880    2.2570    0.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7608    3.2316   -1.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 12 14  1  0
 10 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22  4  1  0
 20  6  1  0
 18  9  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 21 50  1  0
 21 51  1  0
 22 52  1  0
 23 53  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
12a-12-Hydroxy-7,13-abietadien-18-Oate	Generator
12a-12-Hydroxy-7,13-abietadien-18-Oic acid	Generator
12alpha-12-Hydroxy-7,13-abietadien-18-Oate	Generator
12Α-12-hydroxy-7,13-abietadien-18-Oate	Generator
12Α-12-hydroxy-7,13-abietadien-18-Oic acid	Generator
6-Hydroxy-1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,4b,5,6,10,10a-decahydrophenanthrene-1-carboxylate	HMDB

Chemical Formula

C₂₀H₃₀O₃

Average Molecular Weight

318.4504

Monoisotopic Molecular Weight

318.219494826

IUPAC Name

6-hydroxy-1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,4b,5,6,10,10a-decahydrophenanthrene-1-carboxylic acid

Traditional Name

6-hydroxy-7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid

CAS Registry Number

3484-61-5

SMILES

CC(C)C1=CC2=CCC3C(C)(CCCC3(C)C(O)=O)C2CC1O

InChI Identifier

InChI=1S/C20H30O3/c1-12(2)14-10-13-6-7-17-19(3,15(13)11-16(14)21)8-5-9-20(17,4)18(22)23/h6,10,12,15-17,21H,5,7-9,11H2,1-4H3,(H,22,23)

InChI Key

DYNISIGUMYFVJW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Abietane diterpenoid
Phenanthrene
Hydrophenanthrene
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
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

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0039716)
Cell membrane (HMDB: HMDB0039716)

Cellular substructure

Extracellular (HMDB: HMDB0039716)
Membrane (HMDB: HMDB0039716)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0039716)

Source

Endogenous

Endogenous (HMDB: HMDB0039716)

Animal

Animal (HMDB: HMDB0039716)

Exogenous

Food

Food (HMDB: HMDB0039716)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0039716)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0039716)

Cellular process

Cell signaling (HMDB: HMDB0039716)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0039716)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0039716)

Nutrient

Nutrient (HMDB: HMDB0039716)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0039716)

Emulsifier (HMDB: HMDB0039716)

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.09 g/L	ALOGPS
logP	4.31	ALOGPS
logP	3.72	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	4.47	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	92.73 m³·mol⁻¹	ChemAxon
Polarizability	37.06 Å³	ChemAxon
Number of Rings	3	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]+	176.35	31661259
DarkChem	[M-H]-	170.711	31661259
DeepCCS	[M+H]+	177.955	30932474
DeepCCS	[M-H]-	175.597	30932474
DeepCCS	[M-2H]-	209.313	30932474
DeepCCS	[M+Na]+	184.665	30932474
AllCCS	[M+H]+	179.4	32859911
AllCCS	[M+H-H2O]+	176.4	32859911
AllCCS	[M+NH4]+	182.1	32859911
AllCCS	[M+Na]+	182.9	32859911
AllCCS	[M-H]-	185.0	32859911
AllCCS	[M+Na-2H]-	185.5	32859911
AllCCS	[M+HCOO]-	186.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid	CC(C)C1=CC2=CCC3C(C)(CCCC3(C)C(O)=O)C2CC1O	3994.0	Standard polar	33892256
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid	CC(C)C1=CC2=CCC3C(C)(CCCC3(C)C(O)=O)C2CC1O	2440.4	Standard non polar	33892256
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid	CC(C)C1=CC2=CCC3C(C)(CCCC3(C)C(O)=O)C2CC1O	2660.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid,1TMS,isomer #1	CC(C)C1=CC2=CCC3C(C)(C(=O)O[Si](C)(C)C)CCCC3(C)C2CC1O	2594.5	Semi standard non polar	33892256
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid,1TMS,isomer #2	CC(C)C1=CC2=CCC3C(C)(C(=O)O)CCCC3(C)C2CC1O[Si](C)(C)C	2734.3	Semi standard non polar	33892256
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid,2TMS,isomer #1	CC(C)C1=CC2=CCC3C(C)(C(=O)O[Si](C)(C)C)CCCC3(C)C2CC1O[Si](C)(C)C	2631.0	Semi standard non polar	33892256
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid,1TBDMS,isomer #1	CC(C)C1=CC2=CCC3C(C)(C(=O)O[Si](C)(C)C(C)(C)C)CCCC3(C)C2CC1O	2882.9	Semi standard non polar	33892256
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid,1TBDMS,isomer #2	CC(C)C1=CC2=CCC3C(C)(C(=O)O)CCCC3(C)C2CC1O[Si](C)(C)C(C)(C)C	2973.9	Semi standard non polar	33892256
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid,2TBDMS,isomer #1	CC(C)C1=CC2=CCC3C(C)(C(=O)O[Si](C)(C)C(C)(C)C)CCCC3(C)C2CC1O[Si](C)(C)C(C)(C)C	3142.4	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 - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0udi-0293000000-4200ef95fee5bd7b23fe	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid GC-MS (2 TMS) - 70eV, Positive	splash10-0092-6056900000-a222a3dbd5c29194dfbc	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 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 - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 10V, Positive-QTOF	splash10-0uxr-0059000000-dc6b970161db2f6b6ce0	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 20V, Positive-QTOF	splash10-0pir-1193000000-3df9d9610520ada665ad	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 40V, Positive-QTOF	splash10-00ku-2950000000-2beeb3cd4af8fe1feb24	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 10V, Negative-QTOF	splash10-014i-0069000000-ff95f06d050be29f0585	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 20V, Negative-QTOF	splash10-06di-0093000000-787c045cf1ec7607fa3b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 40V, Negative-QTOF	splash10-0ab9-1091000000-568f1bb760d9d3285cfc	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 10V, Negative-QTOF	splash10-014i-0009000000-062ad2a35e11d303cf23	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 20V, Negative-QTOF	splash10-014i-0039000000-b90f2d4ab6f2bcb687ee	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 40V, Negative-QTOF	splash10-00lg-2092000000-a14ccd9e0c63f8bab033	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 10V, Positive-QTOF	splash10-01b9-0097000000-afb143c13652c151b365	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 20V, Positive-QTOF	splash10-0q2a-0091000000-55b97dd7a14931e5e837	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid 40V, Positive-QTOF	splash10-060r-3930000000-4840a56898055317cf58	2021-09-24	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

FDB019352

KNApSAcK ID

Not Available

Chemspider ID

254332

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

288368

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 12alpha-12-Hydroxy-7,13-abietadien-18-oic acid (HMDB0039716)

MOL for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

3D MOL for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

3D SDF for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

3D-SDF for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

PDB for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

3D PDB for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

SMILES for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

INCHI for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

Structure for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

3D Structure for HMDB0039716 (12alpha-12-Hydroxy-7,13-abietadien-18-oic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra