Methylphytol

Details

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Internal ID a081a0ed-e599-4fd5-abbe-4ce23f36abf7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (E,7R,11R)-3,7,11,15-tetramethylheptadec-2-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H42O/c1-6-18(2)10-7-11-19(3)12-8-13-20(4)14-9-15-21(5)16-17-22/h16,18-20,22H,6-15,17H2,1-5H3/b21-16+/t18?,19-,20-/m1/s1
InChI Key WGPDWTXIMJHLLH-KFNBGFFQSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H42O
Molecular Weight 310.60 g/mol
Exact Mass 310.323565959 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 8.70
Atomic LogP (AlogP) 6.75
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methylphytol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.8587 85.87%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.6495 64.95%
OATP2B1 inhibitior - 0.8510 85.10%
OATP1B1 inhibitior + 0.9106 91.06%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6615 66.15%
P-glycoprotein inhibitior - 0.8337 83.37%
P-glycoprotein substrate - 0.8356 83.56%
CYP3A4 substrate - 0.6128 61.28%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.8252 82.52%
CYP2C9 inhibition - 0.8915 89.15%
CYP2C19 inhibition - 0.8921 89.21%
CYP2D6 inhibition - 0.8907 89.07%
CYP1A2 inhibition - 0.7932 79.32%
CYP2C8 inhibition - 0.9501 95.01%
CYP inhibitory promiscuity - 0.6182 61.82%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6321 63.21%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.5827 58.27%
Skin irritation + 0.6349 63.49%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.7923 79.23%
Human Ether-a-go-go-Related Gene inhibition + 0.7745 77.45%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation + 0.8664 86.64%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.6456 64.56%
Acute Oral Toxicity (c) III 0.8431 84.31%
Estrogen receptor binding - 0.5856 58.56%
Androgen receptor binding - 0.7729 77.29%
Thyroid receptor binding + 0.6712 67.12%
Glucocorticoid receptor binding - 0.6333 63.33%
Aromatase binding - 0.5693 56.93%
PPAR gamma - 0.4942 49.42%
Honey bee toxicity - 0.9749 97.49%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9577 95.77%

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
CHEMBL2581 P07339 Cathepsin D 90.65% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.95% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.92% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.27% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.94% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 83.38% 87.45%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.00% 92.86%
CHEMBL3401 O75469 Pregnane X receptor 80.67% 94.73%

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.
Akebia trifoliata
Neolitsea sericea

Cross-Links

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PubChem 129664483
LOTUS LTS0216652
wikiData Q105124757