1,6,6-trimethyl-4-propan-2-ylidene-2,5,7,7a-tetrahydro-1H-indene

Details

Top
Internal ID 4b11a9f8-6c0c-4d9f-aadf-464f30debffc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,6,6-trimethyl-4-propan-2-ylidene-2,5,7,7a-tetrahydro-1H-indene
SMILES (Canonical) CC1CC=C2C1CC(CC2=C(C)C)(C)C
SMILES (Isomeric) CC1CC=C2C1CC(CC2=C(C)C)(C)C
InChI InChI=1S/C15H24/c1-10(2)13-8-15(4,5)9-14-11(3)6-7-12(13)14/h7,11,14H,6,8-9H2,1-5H3
InChI Key INOXZQPYSRQSRK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1,6,6-trimethyl-4-propan-2-ylidene-2,5,7,7a-tetrahydro-1H-indene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.8228 82.28%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.7350 73.50%
OATP2B1 inhibitior - 0.8490 84.90%
OATP1B1 inhibitior + 0.9221 92.21%
OATP1B3 inhibitior + 0.9554 95.54%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9586 95.86%
P-glycoprotein inhibitior - 0.9400 94.00%
P-glycoprotein substrate - 0.8149 81.49%
CYP3A4 substrate - 0.5175 51.75%
CYP2C9 substrate - 0.8001 80.01%
CYP2D6 substrate - 0.7763 77.63%
CYP3A4 inhibition - 0.7336 73.36%
CYP2C9 inhibition - 0.7647 76.47%
CYP2C19 inhibition - 0.7147 71.47%
CYP2D6 inhibition - 0.8976 89.76%
CYP1A2 inhibition - 0.8315 83.15%
CYP2C8 inhibition - 0.9060 90.60%
CYP inhibitory promiscuity - 0.6337 63.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6836 68.36%
Carcinogenicity (trinary) Warning 0.4953 49.53%
Eye corrosion - 0.8744 87.44%
Eye irritation + 0.7933 79.33%
Skin irritation + 0.5526 55.26%
Skin corrosion - 0.9566 95.66%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7620 76.20%
Micronuclear - 0.9626 96.26%
Hepatotoxicity - 0.5196 51.96%
skin sensitisation + 0.8265 82.65%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.5412 54.12%
Nephrotoxicity - 0.5522 55.22%
Acute Oral Toxicity (c) III 0.6797 67.97%
Estrogen receptor binding - 0.9237 92.37%
Androgen receptor binding - 0.7560 75.60%
Thyroid receptor binding - 0.7584 75.84%
Glucocorticoid receptor binding - 0.9055 90.55%
Aromatase binding - 0.8486 84.86%
PPAR gamma - 0.8485 84.85%
Honey bee toxicity - 0.8939 89.39%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5300 53.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.77% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.60% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.26% 97.25%
CHEMBL2581 P07339 Cathepsin D 85.26% 98.95%
CHEMBL4208 P20618 Proteasome component C5 84.03% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.56% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.06% 97.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.63% 90.24%

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.
Conocephalum conicum

Cross-Links

Top
PubChem 101418024
LOTUS LTS0087242
wikiData Q105116327