18-Rabieta-8,11,13-triene-4,15-diol

Details

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Internal ID e78c49c8-d335-4031-a485-d539a17874f3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol
SMILES (Canonical) CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)O
SMILES (Isomeric) CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)O
InChI InChI=1S/C19H28O2/c1-17(2,20)14-7-8-15-13(12-14)6-9-16-18(15,3)10-5-11-19(16,4)21/h7-8,12,16,20-21H,5-6,9-11H2,1-4H3
InChI Key NYEXXEJYGVAGEE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H28O2
Molecular Weight 288.40 g/mol
Exact Mass 288.208930132 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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203455-81-6

2D Structure

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2D Structure of 18-Rabieta-8,11,13-triene-4,15-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9072 90.72%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7035 70.35%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.9169 91.69%
OATP1B3 inhibitior + 0.9501 95.01%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6517 65.17%
P-glycoprotein inhibitior - 0.9064 90.64%
P-glycoprotein substrate - 0.7712 77.12%
CYP3A4 substrate + 0.6001 60.01%
CYP2C9 substrate + 0.6532 65.32%
CYP2D6 substrate + 0.3555 35.55%
CYP3A4 inhibition - 0.8722 87.22%
CYP2C9 inhibition - 0.8584 85.84%
CYP2C19 inhibition - 0.8083 80.83%
CYP2D6 inhibition - 0.9324 93.24%
CYP1A2 inhibition + 0.7047 70.47%
CYP2C8 inhibition + 0.5688 56.88%
CYP inhibitory promiscuity - 0.8837 88.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6511 65.11%
Carcinogenicity (trinary) Non-required 0.6319 63.19%
Eye corrosion - 0.9791 97.91%
Eye irritation - 0.8552 85.52%
Skin irritation - 0.6183 61.83%
Skin corrosion - 0.9492 94.92%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4528 45.28%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6813 68.13%
skin sensitisation - 0.5964 59.64%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8788 87.88%
Acute Oral Toxicity (c) III 0.8967 89.67%
Estrogen receptor binding + 0.5464 54.64%
Androgen receptor binding + 0.6083 60.83%
Thyroid receptor binding + 0.7806 78.06%
Glucocorticoid receptor binding + 0.6538 65.38%
Aromatase binding + 0.6487 64.87%
PPAR gamma + 0.6746 67.46%
Honey bee toxicity - 0.9550 95.50%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9733 97.33%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.27% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.74% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.68% 92.94%
CHEMBL2581 P07339 Cathepsin D 89.37% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.34% 93.99%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.14% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.84% 86.33%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.85% 93.04%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.32% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.13% 95.56%
CHEMBL4581 P52732 Kinesin-like protein 1 84.32% 93.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.76% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.27% 97.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.09% 95.78%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.76% 96.09%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.83% 100.00%

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.
Larix kaempferi
Pinus yunnanensis

Cross-Links

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PubChem 73069324
LOTUS LTS0139452
wikiData Q105187477