CID 78409313

Details

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Internal ID b6093f49-2739-4b73-b57f-4d4980886b1e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 3-methyldec-3-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H22O/c1-3-4-5-6-7-8-11(2)9-10-12/h8,12H,3-7,9-10H2,1-2H3
InChI Key IIHSHWXQNLODTC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H22O
Molecular Weight 170.29 g/mol
Exact Mass 170.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.29
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 78409313

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.9692 96.92%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Lysosomes 0.7160 71.60%
OATP2B1 inhibitior - 0.8457 84.57%
OATP1B1 inhibitior + 0.8694 86.94%
OATP1B3 inhibitior + 0.9354 93.54%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8147 81.47%
P-glycoprotein inhibitior - 0.9699 96.99%
P-glycoprotein substrate - 0.8992 89.92%
CYP3A4 substrate - 0.6390 63.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.8319 83.19%
CYP2C9 inhibition - 0.9353 93.53%
CYP2C19 inhibition - 0.9274 92.74%
CYP2D6 inhibition - 0.9197 91.97%
CYP1A2 inhibition - 0.7152 71.52%
CYP2C8 inhibition - 0.8904 89.04%
CYP inhibitory promiscuity - 0.8118 81.18%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7022 70.22%
Eye corrosion + 0.4945 49.45%
Eye irritation + 0.9485 94.85%
Skin irritation + 0.6091 60.91%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis - 0.9323 93.23%
Human Ether-a-go-go-Related Gene inhibition - 0.4215 42.15%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5996 59.96%
skin sensitisation + 0.8783 87.83%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6336 63.36%
Acute Oral Toxicity (c) III 0.9121 91.21%
Estrogen receptor binding - 0.9405 94.05%
Androgen receptor binding - 0.7920 79.20%
Thyroid receptor binding - 0.8480 84.80%
Glucocorticoid receptor binding - 0.8301 83.01%
Aromatase binding - 0.8542 85.42%
PPAR gamma - 0.7345 73.45%
Honey bee toxicity - 0.9837 98.37%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity + 0.6185 61.85%
Fish aquatic toxicity + 0.8490 84.90%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 98.90% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.61% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 93.50% 97.29%
CHEMBL2581 P07339 Cathepsin D 93.00% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.39% 92.86%
CHEMBL2885 P07451 Carbonic anhydrase III 89.38% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.31% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.91% 91.81%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.84% 91.11%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.42% 100.00%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 81.66% 85.40%
CHEMBL3401 O75469 Pregnane X receptor 80.72% 94.73%
CHEMBL299 P17252 Protein kinase C alpha 80.26% 98.03%

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.
Vachellia farnesiana var. farnesiana

Cross-Links

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PubChem 78409313
LOTUS LTS0093675
wikiData Q105113487