2,3,4,5,6,7-Hexahydro-1beta,6,6-trimethyl-4-(1-methylethylidene)-1H-indene

Details

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Internal ID c0458020-d473-432c-a5fd-71532f31d8ad
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3S)-3,5,5-trimethyl-7-propan-2-ylidene-2,3,4,6-tetrahydro-1H-indene
SMILES (Canonical) CC1CCC2=C1CC(CC2=C(C)C)(C)C
SMILES (Isomeric) C[C@H]1CCC2=C1CC(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/h11H,6-9H2,1-5H3/t11-/m0/s1
InChI Key XLVUTANZHOECMR-NSHDSACASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,3,4,5,6,7-Hexahydro-1beta,6,6-trimethyl-4-(1-methylethylidene)-1H-indene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.8937 89.37%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.7186 71.86%
OATP2B1 inhibitior - 0.8448 84.48%
OATP1B1 inhibitior + 0.9463 94.63%
OATP1B3 inhibitior + 0.9521 95.21%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9361 93.61%
P-glycoprotein inhibitior - 0.9403 94.03%
P-glycoprotein substrate - 0.8762 87.62%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8001 80.01%
CYP2D6 substrate - 0.7763 77.63%
CYP3A4 inhibition - 0.9005 90.05%
CYP2C9 inhibition - 0.7302 73.02%
CYP2C19 inhibition - 0.6980 69.80%
CYP2D6 inhibition - 0.9335 93.35%
CYP1A2 inhibition - 0.8114 81.14%
CYP2C8 inhibition - 0.8706 87.06%
CYP inhibitory promiscuity - 0.6924 69.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Warning 0.4740 47.40%
Eye corrosion - 0.9232 92.32%
Eye irritation + 0.9253 92.53%
Skin irritation + 0.5325 53.25%
Skin corrosion - 0.9756 97.56%
Ames mutagenesis - 0.7354 73.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3951 39.51%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.8722 87.22%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5455 54.55%
Acute Oral Toxicity (c) III 0.6583 65.83%
Estrogen receptor binding - 0.9381 93.81%
Androgen receptor binding - 0.6410 64.10%
Thyroid receptor binding - 0.7099 70.99%
Glucocorticoid receptor binding - 0.8645 86.45%
Aromatase binding - 0.8922 89.22%
PPAR gamma - 0.8180 81.80%
Honey bee toxicity - 0.8857 88.57%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9974 99.74%

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 95.76% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.43% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.93% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.84% 92.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.87% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.15% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.26% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.09% 95.89%

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.
Conocephalum conicum

Cross-Links

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PubChem 15484924
NPASS NPC179719
LOTUS LTS0067712
wikiData Q105330453