6-epi-Tetrahydrothebaine

Details

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Internal ID 0a888e76-7402-458d-b7c8-a947fdbe3bab
Taxonomy Alkaloids and derivatives > Morphinans
IUPAC Name (4R,4aR,7R,7aR,12bS)-7,9-dimethoxy-3-methyl-2,4,4a,5,6,7,7a,13-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H25NO3/c1-20-9-8-19-12-5-7-15(22-3)18(19)23-17-14(21-2)6-4-11(16(17)19)10-13(12)20/h4,6,12-13,15,18H,5,7-10H2,1-3H3/t12-,13+,15+,18-,19-/m0/s1
InChI Key RVJQWONQPCTLDL-MKUCUKIISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H25NO3
Molecular Weight 315.40 g/mol
Exact Mass 315.18344366 g/mol
Topological Polar Surface Area (TPSA) 30.90 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-epi-Tetrahydrothebaine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 + 0.9589 95.89%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.4968 49.68%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9221 92.21%
OATP1B3 inhibitior + 0.9470 94.70%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7237 72.37%
P-glycoprotein inhibitior - 0.7907 79.07%
P-glycoprotein substrate + 0.7678 76.78%
CYP3A4 substrate + 0.7708 77.08%
CYP2C9 substrate - 0.6651 66.51%
CYP2D6 substrate + 0.7554 75.54%
CYP3A4 inhibition - 0.8404 84.04%
CYP2C9 inhibition - 0.9200 92.00%
CYP2C19 inhibition - 0.8015 80.15%
CYP2D6 inhibition + 0.7488 74.88%
CYP1A2 inhibition - 0.8450 84.50%
CYP2C8 inhibition - 0.9280 92.80%
CYP inhibitory promiscuity - 0.8726 87.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6608 66.08%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9891 98.91%
Skin irritation - 0.8330 83.30%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6866 68.66%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8521 85.21%
Respiratory toxicity + 0.9667 96.67%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.7403 74.03%
Acute Oral Toxicity (c) II 0.6544 65.44%
Estrogen receptor binding - 0.6537 65.37%
Androgen receptor binding - 0.6620 66.20%
Thyroid receptor binding + 0.6085 60.85%
Glucocorticoid receptor binding - 0.4914 49.14%
Aromatase binding - 0.7680 76.80%
PPAR gamma - 0.5836 58.36%
Honey bee toxicity - 0.8165 81.65%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity + 0.6588 65.88%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.33% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 94.54% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.49% 95.56%
CHEMBL5203 P33316 dUTP pyrophosphatase 90.12% 99.18%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.95% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.86% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.98% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.37% 97.14%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.83% 89.62%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 84.27% 90.95%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.84% 91.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.69% 86.33%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 82.98% 95.78%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 82.87% 98.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.15% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.72% 100.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.57% 93.40%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.48% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.47% 93.99%
CHEMBL217 P14416 Dopamine D2 receptor 80.74% 95.62%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.45% 93.04%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.06% 97.25%

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.
Papaver somniferum

Cross-Links

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PubChem 20833250
LOTUS LTS0036743
wikiData Q105246077