(3R,4S)-3-ethenyl-3-methyl-6-propan-2-ylidene-4-prop-1-en-2-ylcyclohexene

Details

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Internal ID e89b40a1-01aa-40db-ab5a-a2e4a5120759
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3R,4S)-3-ethenyl-3-methyl-6-propan-2-ylidene-4-prop-1-en-2-ylcyclohexene
SMILES (Canonical) CC(=C1CC(C(C=C1)(C)C=C)C(=C)C)C
SMILES (Isomeric) CC(=C1C[C@H]([C@](C=C1)(C)C=C)C(=C)C)C
InChI InChI=1S/C15H22/c1-7-15(6)9-8-13(11(2)3)10-14(15)12(4)5/h7-9,14H,1,4,10H2,2-3,5-6H3/t14-,15+/m0/s1
InChI Key AXYSUALLGDLVIT-LSDHHAIUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.67
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,4S)-3-ethenyl-3-methyl-6-propan-2-ylidene-4-prop-1-en-2-ylcyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.6294 62.94%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.6596 65.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9173 91.73%
OATP1B3 inhibitior + 0.8620 86.20%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7805 78.05%
P-glycoprotein inhibitior - 0.9404 94.04%
P-glycoprotein substrate - 0.8177 81.77%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.7951 79.51%
CYP3A4 inhibition - 0.7498 74.98%
CYP2C9 inhibition - 0.8491 84.91%
CYP2C19 inhibition - 0.7711 77.11%
CYP2D6 inhibition - 0.9340 93.40%
CYP1A2 inhibition - 0.8460 84.60%
CYP2C8 inhibition - 0.8584 85.84%
CYP inhibitory promiscuity - 0.5666 56.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5083 50.83%
Carcinogenicity (trinary) Non-required 0.4818 48.18%
Eye corrosion + 0.6516 65.16%
Eye irritation + 0.8555 85.55%
Skin irritation + 0.7580 75.80%
Skin corrosion - 0.9401 94.01%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7228 72.28%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.9370 93.70%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.6616 66.16%
Nephrotoxicity + 0.5151 51.51%
Acute Oral Toxicity (c) III 0.7254 72.54%
Estrogen receptor binding - 0.8817 88.17%
Androgen receptor binding - 0.7303 73.03%
Thyroid receptor binding - 0.7882 78.82%
Glucocorticoid receptor binding - 0.7868 78.68%
Aromatase binding - 0.7102 71.02%
PPAR gamma - 0.6808 68.08%
Honey bee toxicity - 0.7772 77.72%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9936 99.36%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.35% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 94.90% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.46% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.50% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.16% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.76% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 82.25% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 81.55% 90.17%
CHEMBL2581 P07339 Cathepsin D 80.21% 98.95%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.02% 85.30%

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.
Baccharis darwinii

Cross-Links

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PubChem 53310786
LOTUS LTS0214926
wikiData Q104920921