Trinoranastreptene

Details

Top
Internal ID 3f62b558-7964-4b41-ba99-a4e99c653576
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (1S,5S,6S)-2,6-dimethyltricyclo[4.4.0.01,5]deca-2,9-diene
SMILES (Canonical) CC1=CCC2C13C2(CCC=C3)C
SMILES (Isomeric) CC1=CC[C@@H]2[C@]13[C@]2(CCC=C3)C
InChI InChI=1S/C12H16/c1-9-5-6-10-11(2)7-3-4-8-12(9,10)11/h4-5,8,10H,3,6-7H2,1-2H3/t10-,11-,12+/m0/s1
InChI Key GOAGZWVCKOCSLC-SDDRHHMPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H16
Molecular Weight 160.25 g/mol
Exact Mass 160.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.31
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
DTXSID001019193
86160-98-7

2D Structure

Top
2D Structure of Trinoranastreptene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.9083 90.83%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.7714 77.14%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9394 93.94%
OATP1B3 inhibitior + 0.9461 94.61%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9377 93.77%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9100 91.00%
CYP3A4 substrate - 0.5330 53.30%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.7566 75.66%
CYP3A4 inhibition - 0.8345 83.45%
CYP2C9 inhibition - 0.7679 76.79%
CYP2C19 inhibition - 0.6632 66.32%
CYP2D6 inhibition - 0.9028 90.28%
CYP1A2 inhibition - 0.7118 71.18%
CYP2C8 inhibition - 0.8296 82.96%
CYP inhibitory promiscuity - 0.5558 55.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.4643 46.43%
Eye corrosion - 0.9463 94.63%
Eye irritation - 0.5357 53.57%
Skin irritation - 0.5806 58.06%
Skin corrosion - 0.9549 95.49%
Ames mutagenesis - 0.7170 71.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4857 48.57%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation + 0.7930 79.30%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5569 55.69%
Acute Oral Toxicity (c) III 0.7848 78.48%
Estrogen receptor binding - 0.9501 95.01%
Androgen receptor binding + 0.5256 52.56%
Thyroid receptor binding - 0.8418 84.18%
Glucocorticoid receptor binding - 0.9224 92.24%
Aromatase binding - 0.8745 87.45%
PPAR gamma - 0.8731 87.31%
Honey bee toxicity - 0.9094 90.94%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 1.0000 100.00%

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 87.97% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.49% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 85.05% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.88% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.62% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.24% 97.09%

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.
Calypogeia granulata

Cross-Links

Top
PubChem 154735202
LOTUS LTS0082086
wikiData Q105013570