Cannithrene 2

Details

Top
Internal ID 970ea8ce-0c9b-4cee-98d4-f1e84f156a1b
Taxonomy Benzenoids > Phenanthrenes and derivatives > Hydrophenanthrenes
IUPAC Name 2,6-dimethoxy-9,10-dihydrophenanthrene-4,5-diol
SMILES (Canonical) COC1=C(C2=C(CCC3=C2C(=CC(=C3)OC)O)C=C1)O
SMILES (Isomeric) COC1=C(C2=C(CCC3=C2C(=CC(=C3)OC)O)C=C1)O
InChI InChI=1S/C16H16O4/c1-19-11-7-10-4-3-9-5-6-13(20-2)16(18)15(9)14(10)12(17)8-11/h5-8,17-18H,3-4H2,1-2H3
InChI Key JOPGVVOTXYNMIS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C16H16O4
Molecular Weight 272.29 g/mol
Exact Mass 272.10485899 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Cannithrene 2

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9660 96.60%
Caco-2 + 0.8178 81.78%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8068 80.68%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9282 92.82%
OATP1B3 inhibitior + 0.9729 97.29%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6058 60.58%
P-glycoprotein inhibitior - 0.8230 82.30%
P-glycoprotein substrate - 0.9154 91.54%
CYP3A4 substrate + 0.5059 50.59%
CYP2C9 substrate - 0.6180 61.80%
CYP2D6 substrate + 0.5879 58.79%
CYP3A4 inhibition - 0.8034 80.34%
CYP2C9 inhibition + 0.5721 57.21%
CYP2C19 inhibition + 0.7080 70.80%
CYP2D6 inhibition - 0.7818 78.18%
CYP1A2 inhibition + 0.9583 95.83%
CYP2C8 inhibition + 0.5866 58.66%
CYP inhibitory promiscuity + 0.6155 61.55%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7920 79.20%
Carcinogenicity (trinary) Non-required 0.5256 52.56%
Eye corrosion - 0.9773 97.73%
Eye irritation - 0.5757 57.57%
Skin irritation - 0.5804 58.04%
Skin corrosion - 0.8887 88.87%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4163 41.63%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8298 82.98%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5445 54.45%
Acute Oral Toxicity (c) III 0.5762 57.62%
Estrogen receptor binding + 0.8656 86.56%
Androgen receptor binding + 0.7505 75.05%
Thyroid receptor binding + 0.6840 68.40%
Glucocorticoid receptor binding + 0.8472 84.72%
Aromatase binding + 0.5875 58.75%
PPAR gamma + 0.6303 63.03%
Honey bee toxicity - 0.9552 95.52%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5351 53.51%
Fish aquatic toxicity + 0.9226 92.26%

Targets

Top

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 97.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.42% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.14% 95.56%
CHEMBL4208 P20618 Proteasome component C5 91.44% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 91.15% 91.49%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 89.50% 91.79%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.36% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.16% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.86% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.23% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.52% 99.15%
CHEMBL205 P00918 Carbonic anhydrase II 85.44% 98.44%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.25% 92.68%
CHEMBL2535 P11166 Glucose transporter 84.10% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.98% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.61% 95.89%
CHEMBL2056 P21728 Dopamine D1 receptor 83.29% 91.00%
CHEMBL2581 P07339 Cathepsin D 81.87% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.07% 92.94%

Plants that contains it

Top
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.
Cannabis sativa
Dendrobium nobile
Empetrum nigrum

Cross-Links

Top
PubChem 86021565
LOTUS LTS0233419
wikiData Q105237331