1,1,5,5-tetramethyl-4-methylidene-3,4a,6,7-tetrahydro-2H-naphthalene

Details

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Internal ID cabf1605-5abd-4a77-b414-9f7f5ad035c2
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1,1,5,5-tetramethyl-4-methylidene-3,4a,6,7-tetrahydro-2H-naphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-11-8-10-14(2,3)12-7-6-9-15(4,5)13(11)12/h7,13H,1,6,8-10H2,2-5H3
InChI Key DOTPZZZHOADLRP-UHFFFAOYSA-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 4.60
Atomic LogP (AlogP) 4.73
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 1,1,5,5-tetramethyl-4-methylidene-3,4a,6,7-tetrahydro-2H-naphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.8561 85.61%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.7089 70.89%
OATP2B1 inhibitior - 0.8483 84.83%
OATP1B1 inhibitior + 0.9126 91.26%
OATP1B3 inhibitior + 0.8356 83.56%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9118 91.18%
P-glycoprotein inhibitior - 0.9085 90.85%
P-glycoprotein substrate - 0.9389 93.89%
CYP3A4 substrate - 0.5384 53.84%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.8826 88.26%
CYP2C9 inhibition - 0.6712 67.12%
CYP2C19 inhibition - 0.5623 56.23%
CYP2D6 inhibition - 0.9054 90.54%
CYP1A2 inhibition - 0.8300 83.00%
CYP2C8 inhibition - 0.7645 76.45%
CYP inhibitory promiscuity - 0.6428 64.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.4666 46.66%
Eye corrosion - 0.9366 93.66%
Eye irritation + 0.9419 94.19%
Skin irritation - 0.6147 61.47%
Skin corrosion - 0.9481 94.81%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6619 66.19%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5662 56.62%
skin sensitisation + 0.8220 82.20%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6009 60.09%
Acute Oral Toxicity (c) III 0.8084 80.84%
Estrogen receptor binding - 0.8957 89.57%
Androgen receptor binding - 0.5591 55.91%
Thyroid receptor binding - 0.7297 72.97%
Glucocorticoid receptor binding - 0.6988 69.88%
Aromatase binding - 0.6007 60.07%
PPAR gamma - 0.8574 85.74%
Honey bee toxicity - 0.8799 87.99%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.22% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.47% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.13% 96.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.08% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.68% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.43% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.95% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.60% 92.94%

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.
Holarrhena pubescens

Cross-Links

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PubChem 5321892
NPASS NPC172931