3-(4,8,12,16,20-Pentamethylhenicosa-3,7,11,15,19-pentaenyl)furan

Details

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Internal ID beae51e2-6d69-471e-9d78-534a4d0ae818
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name 3-(4,8,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)furan
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC1=COC=C1)C)C)C)C)C
SMILES (Isomeric) CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC1=COC=C1)C)C)C)C)C
InChI InChI=1S/C30H46O/c1-25(2)12-7-13-26(3)14-8-15-27(4)16-9-17-28(5)18-10-19-29(6)20-11-21-30-22-23-31-24-30/h12,14,16,18,20,22-24H,7-11,13,15,17,19,21H2,1-6H3
InChI Key LOJYRXSXXRYRCN-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H46O
Molecular Weight 422.70 g/mol
Exact Mass 422.354866087 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 10.60
Atomic LogP (AlogP) 10.08
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4,8,12,16,20-Pentamethylhenicosa-3,7,11,15,19-pentaenyl)furan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.5188 51.88%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Nucleus 0.4321 43.21%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.7933 79.33%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9082 90.82%
P-glycoprotein inhibitior + 0.8062 80.62%
P-glycoprotein substrate - 0.9114 91.14%
CYP3A4 substrate - 0.5577 55.77%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.6885 68.85%
CYP3A4 inhibition - 0.9172 91.72%
CYP2C9 inhibition - 0.7389 73.89%
CYP2C19 inhibition - 0.6220 62.20%
CYP2D6 inhibition - 0.8916 89.16%
CYP1A2 inhibition + 0.5126 51.26%
CYP2C8 inhibition - 0.7986 79.86%
CYP inhibitory promiscuity + 0.5714 57.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.4191 41.91%
Eye corrosion - 0.7359 73.59%
Eye irritation - 0.8749 87.49%
Skin irritation + 0.6517 65.17%
Skin corrosion - 0.9254 92.54%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7546 75.46%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.8158 81.58%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5841 58.41%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.5628 56.28%
Acute Oral Toxicity (c) III 0.8464 84.64%
Estrogen receptor binding - 0.5585 55.85%
Androgen receptor binding - 0.6927 69.27%
Thyroid receptor binding + 0.5657 56.57%
Glucocorticoid receptor binding - 0.4886 48.86%
Aromatase binding - 0.5187 51.87%
PPAR gamma + 0.7680 76.80%
Honey bee toxicity - 0.9278 92.78%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6232 62.32%
Fish aquatic toxicity + 0.9887 98.87%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 97.67% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 93.44% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.07% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.57% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.12% 98.95%
CHEMBL2039 P27338 Monoamine oxidase B 88.04% 92.51%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.34% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.21% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.83% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 71437261
LOTUS LTS0180768
wikiData Q105154768