8a-Methyl-5-methylidene-3-propan-2-yl-1,2,3,3a,4,6,7,8-octahydroazulene-4,8-diol

Details

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Internal ID db89f9ca-f8df-4873-82bc-2ce1130f97b0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 8a-methyl-5-methylidene-3-propan-2-yl-1,2,3,3a,4,6,7,8-octahydroazulene-4,8-diol
SMILES (Canonical) CC(C)C1CCC2(C1C(C(=C)CCC2O)O)C
SMILES (Isomeric) CC(C)C1CCC2(C1C(C(=C)CCC2O)O)C
InChI InChI=1S/C15H26O2/c1-9(2)11-7-8-15(4)12(16)6-5-10(3)14(17)13(11)15/h9,11-14,16-17H,3,5-8H2,1-2,4H3
InChI Key YYJZEVFUWRXYOT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.75
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8a-Methyl-5-methylidene-3-propan-2-yl-1,2,3,3a,4,6,7,8-octahydroazulene-4,8-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.4943 49.43%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.5120 51.20%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.9176 91.76%
OATP1B3 inhibitior + 0.8629 86.29%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9401 94.01%
P-glycoprotein inhibitior - 0.9025 90.25%
P-glycoprotein substrate - 0.8792 87.92%
CYP3A4 substrate + 0.5649 56.49%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8510 85.10%
CYP2C9 inhibition - 0.8043 80.43%
CYP2C19 inhibition - 0.7694 76.94%
CYP2D6 inhibition - 0.9396 93.96%
CYP1A2 inhibition - 0.6270 62.70%
CYP2C8 inhibition - 0.8785 87.85%
CYP inhibitory promiscuity - 0.8279 82.79%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5960 59.60%
Eye corrosion - 0.9808 98.08%
Eye irritation - 0.5317 53.17%
Skin irritation + 0.5957 59.57%
Skin corrosion - 0.9466 94.66%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6424 64.24%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6008 60.08%
skin sensitisation + 0.5344 53.44%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.7998 79.98%
Acute Oral Toxicity (c) III 0.6144 61.44%
Estrogen receptor binding - 0.5569 55.69%
Androgen receptor binding + 0.5469 54.69%
Thyroid receptor binding - 0.6138 61.38%
Glucocorticoid receptor binding - 0.6383 63.83%
Aromatase binding - 0.7584 75.84%
PPAR gamma - 0.8377 83.77%
Honey bee toxicity - 0.9124 91.24%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9774 97.74%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 93.26% 96.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.67% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.73% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 89.65% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.38% 95.89%
CHEMBL1871 P10275 Androgen Receptor 88.22% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.61% 96.09%
CHEMBL204 P00734 Thrombin 86.85% 96.01%
CHEMBL1937 Q92769 Histone deacetylase 2 85.91% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.35% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.80% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.20% 82.69%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Artabotrys monteiroae
Jacobaea erucifolia subsp. argunensis

Cross-Links

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PubChem 75221124
LOTUS LTS0248339
wikiData Q105368692