Hinesene

Details

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Internal ID 7a9e0840-c83d-4f0b-b1e0-25f46ccd84ac
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3R,5S,6S)-6,10-dimethyl-3-prop-1-en-2-ylspiro[4.5]dec-9-ene
SMILES (Canonical) CC1CCC=C(C12CCC(C2)C(=C)C)C
SMILES (Isomeric) C[C@H]1CCC=C([C@]12CC[C@H](C2)C(=C)C)C
InChI InChI=1S/C15H24/c1-11(2)14-8-9-15(10-14)12(3)6-5-7-13(15)4/h6,13-14H,1,5,7-10H2,2-4H3/t13-,14+,15+/m0/s1
InChI Key WEZDOYDDKIHCLM-RRFJBIMHSA-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 5.40
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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WEZDOYDDKIHCLM-RRFJBIMHSA-N
Q67879919

2D Structure

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2D Structure of Hinesene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 + 0.8182 81.82%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.8002 80.02%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.9571 95.71%
OATP1B3 inhibitior + 0.8923 89.23%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8100 81.00%
P-glycoprotein inhibitior - 0.9542 95.42%
P-glycoprotein substrate - 0.8107 81.07%
CYP3A4 substrate - 0.5209 52.09%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.7620 76.20%
CYP3A4 inhibition - 0.8453 84.53%
CYP2C9 inhibition - 0.8128 81.28%
CYP2C19 inhibition - 0.7747 77.47%
CYP2D6 inhibition - 0.9423 94.23%
CYP1A2 inhibition - 0.8103 81.03%
CYP2C8 inhibition - 0.8261 82.61%
CYP inhibitory promiscuity - 0.7992 79.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Warning 0.5123 51.23%
Eye corrosion - 0.8186 81.86%
Eye irritation + 0.6337 63.37%
Skin irritation + 0.6416 64.16%
Skin corrosion - 0.9869 98.69%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5575 55.75%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6448 64.48%
skin sensitisation + 0.8626 86.26%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.6195 61.95%
Acute Oral Toxicity (c) III 0.8589 85.89%
Estrogen receptor binding - 0.8947 89.47%
Androgen receptor binding - 0.7495 74.95%
Thyroid receptor binding - 0.8196 81.96%
Glucocorticoid receptor binding - 0.6278 62.78%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.6935 69.35%
Honey bee toxicity - 0.9101 91.01%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.5300 53.00%
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 91.49% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.29% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.01% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.23% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.80% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 87.51% 86.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.39% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.73% 93.04%
CHEMBL221 P23219 Cyclooxygenase-1 81.48% 90.17%
CHEMBL4208 P20618 Proteasome component C5 81.17% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.11% 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.
Rolandra fruticosa

Cross-Links

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PubChem 11310242
LOTUS LTS0150975
wikiData Q67879919