(6R,10S)-6,10,14-trimethylpentadecanal

Details

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Internal ID f6d41950-6f87-4bc4-b985-7cb87d2c060c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (6R,10S)-6,10,14-trimethylpentadecanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H36O/c1-16(2)10-8-12-18(4)14-9-13-17(3)11-6-5-7-15-19/h15-18H,5-14H2,1-4H3/t17-,18+/m1/s1
InChI Key UTAMACDSDSDLHB-MSOLQXFVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H36O
Molecular Weight 268.50 g/mol
Exact Mass 268.276615768 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 7.30
Atomic LogP (AlogP) 6.01
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6R,10S)-6,10,14-trimethylpentadecanal

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 + 0.8190 81.90%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4564 45.64%
OATP2B1 inhibitior - 0.8493 84.93%
OATP1B1 inhibitior + 0.9512 95.12%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.4801 48.01%
P-glycoprotein inhibitior - 0.8410 84.10%
P-glycoprotein substrate - 0.8239 82.39%
CYP3A4 substrate - 0.6199 61.99%
CYP2C9 substrate - 0.5862 58.62%
CYP2D6 substrate - 0.7805 78.05%
CYP3A4 inhibition - 0.9858 98.58%
CYP2C9 inhibition - 0.9361 93.61%
CYP2C19 inhibition - 0.9618 96.18%
CYP2D6 inhibition - 0.9707 97.07%
CYP1A2 inhibition - 0.6565 65.65%
CYP2C8 inhibition - 0.9901 99.01%
CYP inhibitory promiscuity - 0.9447 94.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.7450 74.50%
Eye corrosion + 0.9889 98.89%
Eye irritation + 0.8015 80.15%
Skin irritation + 0.7665 76.65%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5481 54.81%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation + 0.9322 93.22%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity - 0.9549 95.49%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.5754 57.54%
Acute Oral Toxicity (c) III 0.8417 84.17%
Estrogen receptor binding - 0.6098 60.98%
Androgen receptor binding - 0.8778 87.78%
Thyroid receptor binding + 0.7199 71.99%
Glucocorticoid receptor binding - 0.5916 59.16%
Aromatase binding - 0.5297 52.97%
PPAR gamma - 0.5213 52.13%
Honey bee toxicity - 0.9475 94.75%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8790 87.90%

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 92.94% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 88.58% 93.31%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.99% 89.34%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.45% 97.29%
CHEMBL3401 O75469 Pregnane X receptor 86.09% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.64% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.60% 96.47%
CHEMBL230 P35354 Cyclooxygenase-2 84.86% 89.63%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.64% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.60% 96.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.16% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.43% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.71% 95.56%

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.
Sideritis hirsuta

Cross-Links

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PubChem 163185756
LOTUS LTS0022412
wikiData Q105278647