MiMeDB: Showing metabocard for 12-hydroxyalbrassitriol (MMDBc0024091)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 13:56:54 UTC

Update Date

2025-10-07 16:07:24 UTC

Metabolite ID

MMDBc0024091

Metabolite Identification

Common Name

12-hydroxyalbrassitriol

Description

12-hydroxyalbrassitriol is a drimane sesquiterpenoid, a chemical class characterized by a specific arrangement of carbon atoms and functional groups. Its chemical structure features a hydroxyl group at the 12-position, which is significant in determining its reactivity and interactions. This compound was isolated from cultures of the fungus Penicillium sp., highlighting its potential as a natural product with unique chemical properties (PMID:27892687 ). In terms of biological pathways, sesquiterpenoids like 12-hydroxyalbrassitriol are often involved in various metabolic processes, including those related to plant defense mechanisms and interactions with other organisms. They can also play roles in signaling pathways within fungi and plants, contributing to ecological interactions. The presence of hydroxyl groups in such compounds often enhances their solubility and biological activity, facilitating their involvement in diverse biochemical pathways. Overall, 12-hydroxyalbrassitriol exemplifies the complexity and significance of natural products derived from fungi, offering insights into both chemistry and potential biological applications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152115562D          

 21 22  0  0  1  0            999 V2000
    1.9592    0.1930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986    0.1930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3882    3.1070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1060    3.8822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276    3.1070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  6  4  1  0  0  0  0
 10  7  2  0  0  0  0
 10  8  1  0  0  0  0
 11  7  1  0  0  0  0
 12 11  1  0  0  0  0
 13  1  1  0  0  0  0
 13  2  1  0  0  0  0
 13  5  1  0  0  0  0
 13 12  1  0  0  0  0
 14  3  1  1  0  0  0
 14  6  1  0  0  0  0
 14 12  1  0  0  0  0
 15  9  1  1  0  0  0
 15 10  1  0  0  0  0
 15 14  1  0  0  0  0
 16  8  1  0  0  0  0
 17  9  1  0  0  0  0
 11 18  1  6  0  0  0
 15 19  1  6  0  0  0
 11 20  1  1  0  0  0
 12 21  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0024091

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]1(O)C=C(CO)[C@](O)(CO)[C@@]2(C)CCCC(C)(C)[C@]12[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O4/c1-13(2)5-4-6-14(3)12(13)11(18)7-10(8-16)15(14,19)9-17/h7,11-12,16-19H,4-6,8-9H2,1-3H3/t11-,12-,14-,15+/m0/s1

> <INCHI_KEY>
HUZKUSWQRONLOJ-NZBPQXDJSA-N

> <FORMULA>
C15H26O4

> <MOLECULAR_WEIGHT>
270.369

> <EXACT_MASS>
270.183109317

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
29.973559231618836

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4S,4aS,8aS)-1,2-bis(hydroxymethyl)-5,5,8a-trimethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalene-1,4-diol

> <ALOGPS_LOGP>
1.12

> <JCHEM_LOGP>
0.16054916233333297

> <ALOGPS_LOGS>
-1.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.373845658814432

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.982165160781143

> <JCHEM_PKA_STRONGEST_BASIC>
-2.771088405469177

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
73.757

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.78e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,4aS,8aS)-1,2-bis(hydroxymethyl)-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalene-1,4-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       3.657   0.360   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.677   0.360   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.325   5.800   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.336   3.850   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       5.798   7.247   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       4.345   5.800   0.000  0.00  0.00           O+0
HETATM   20  H   UNK     0       4.001   0.770   0.000  0.00  0.00           H+0
HETATM   21  H   UNK     0       2.667   3.080   0.000  0.00  0.00           H+0
CONECT    1   13                                                            
CONECT    2   13                                                            
CONECT    3   14                                                            
CONECT    4    5    6                                                       
CONECT    5    4   13                                                       
CONECT    6    4   14                                                       
CONECT    7   10   11                                                       
CONECT    8   10   16                                                       
CONECT    9   15   17                                                       
CONECT   10    7    8   15                                                  
CONECT   11    7   12   18   20                                             
CONECT   12   11   13   14   21                                             
CONECT   13    1    2    5   12                                             
CONECT   14    3    6   12   15                                             
CONECT   15    9   10   14   19                                             
CONECT   16    8                                                            
CONECT   17    9                                                            
CONECT   18   11                                                            
CONECT   19   15                                                            
CONECT   20   11                                                            
CONECT   21   12                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

Synonyms

Not Available

Molecular Formula

C₁₅H₂₆O₄

Average Mass

270.369

Monoisotopic Mass

270.183109317

IUPAC Name

(1S,4S,4aS,8aS)-1,2-bis(hydroxymethyl)-5,5,8a-trimethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalene-1,4-diol

Traditional Name

(1S,4S,4aS,8aS)-1,2-bis(hydroxymethyl)-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalene-1,4-diol

CAS Registry Number

Not Available

SMILES

[H][C@]1(O)C=C(CO)[C@](O)(CO)[C@@]2(C)CCCC(C)(C)[C@]12[H]

InChI Identifier

InChI=1S/C15H26O4/c1-13(2)5-4-6-14(3)12(13)11(18)7-10(8-16)15(14,19)9-17/h7,11-12,16-19H,4-6,8-9H2,1-3H3/t11-,12-,14-,15+/m0/s1

InChI Key

HUZKUSWQRONLOJ-NZBPQXDJSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Tertiary alcohols

Alternative Parents

Substituents

Tertiary alcohol
Secondary alcohol
Hydrocarbon derivative
Primary alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	4.78 g/L	ALOGPS
logP	1.12	ALOGPS
logP	0.16	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	12.98	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	73.76 m³·mol⁻¹	ChemAxon
Polarizability	29.97 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

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	2	Human feces	Metabolic reconstruction; Microbial culture

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78439428

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139591336

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

HUZKUSWQRONLOJ-NZBPQXDJSA-N

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for 12-hydroxyalbrassitriol (MMDBc0024091)

MOL for #<Metabolite:0x00007f8d7f48cad8>

3D MOL for #<Metabolite:0x00007f8d7f48cad8>

3D SDF for #<Metabolite:0x00007f8d7f48cad8>

3D-SDF for #<Metabolite:0x00007f8d7f48cad8>

PDB for #<Metabolite:0x00007f8d7f48cad8>

3D PDB for #<Metabolite:0x00007f8d7f48cad8>

SMILES for #<Metabolite:0x00007f8d7f48cad8>

INCHI for #<Metabolite:0x00007f8d7f48cad8>

Structure for #<Metabolite:0x00007f8d7f48cad8>

3D Structure for #<Metabolite:0x00007f8d7f48cad8>