(Z)-2-Methyloct-3-en-2-ol

Details

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Internal ID c0506ada-2d82-4903-816c-73c9fca75b87
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (Z)-2-methyloct-3-en-2-ol
SMILES (Canonical) CCCCC=CC(C)(C)O
SMILES (Isomeric) CCCC/C=C\C(C)(C)O
InChI InChI=1S/C9H18O/c1-4-5-6-7-8-9(2,3)10/h7-8,10H,4-6H2,1-3H3/b8-7-
InChI Key ACFQKNIZLQUKQA-FPLPWBNLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18O
Molecular Weight 142.24 g/mol
Exact Mass 142.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.50
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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18521-07-8
(Z)-2-methyl-3-octen-2-ol
3-Octen-2-ol, 2-methyl-, (Z)-
EINECS 242-395-4
DTXSID70879629
ACFQKNIZLQUKQA-FPLPWBNLSA-N
(3Z)-2-Methyl-3-octen-2-ol

2D Structure

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2D Structure of (Z)-2-Methyloct-3-en-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9862 98.62%
Caco-2 + 0.9815 98.15%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.3690 36.90%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.8607 86.07%
OATP1B3 inhibitior + 0.9344 93.44%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8702 87.02%
P-glycoprotein inhibitior - 0.9789 97.89%
P-glycoprotein substrate - 0.9296 92.96%
CYP3A4 substrate - 0.6484 64.84%
CYP2C9 substrate - 0.7948 79.48%
CYP2D6 substrate - 0.7612 76.12%
CYP3A4 inhibition - 0.9195 91.95%
CYP2C9 inhibition - 0.8345 83.45%
CYP2C19 inhibition - 0.8409 84.09%
CYP2D6 inhibition - 0.9271 92.71%
CYP1A2 inhibition - 0.6107 61.07%
CYP2C8 inhibition - 0.9140 91.40%
CYP inhibitory promiscuity - 0.6152 61.52%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6463 64.63%
Eye corrosion + 0.7841 78.41%
Eye irritation + 0.8517 85.17%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.8043 80.43%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5393 53.93%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation + 0.9372 93.72%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.6113 61.13%
Acute Oral Toxicity (c) III 0.8130 81.30%
Estrogen receptor binding - 0.9468 94.68%
Androgen receptor binding - 0.9067 90.67%
Thyroid receptor binding - 0.7259 72.59%
Glucocorticoid receptor binding - 0.7766 77.66%
Aromatase binding - 0.9441 94.41%
PPAR gamma - 0.7930 79.30%
Honey bee toxicity - 0.9838 98.38%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5468 54.68%
Fish aquatic toxicity + 0.7814 78.14%

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 91.26% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.59% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.10% 98.95%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 87.53% 85.40%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.82% 96.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.58% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.93% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.84% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 82.97% 87.45%
CHEMBL2996 Q05655 Protein kinase C delta 80.57% 97.79%

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.
Centipeda minima

Cross-Links

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PubChem 5366246
NPASS NPC256280