(R)-4-Methyl-1-heptanol

Details

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Internal ID ad75c4ee-1349-46f8-98a4-c80d49da5376
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (4R)-4-methylheptan-1-ol
SMILES (Canonical) CCCC(C)CCCO
SMILES (Isomeric) CCC[C@@H](C)CCCO
InChI InChI=1S/C8H18O/c1-3-5-8(2)6-4-7-9/h8-9H,3-7H2,1-2H3/t8-/m1/s1
InChI Key LLUQZGDMUIMPTC-MRVPVSSYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C8H18O
Molecular Weight 130.23 g/mol
Exact Mass 130.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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(4R)-4-methylheptan-1-ol
SCHEMBL17831605
CHEBI:67887
Q27136363

2D Structure

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2D Structure of (R)-4-Methyl-1-heptanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9242 92.42%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6942 69.42%
OATP2B1 inhibitior - 0.8344 83.44%
OATP1B1 inhibitior + 0.9405 94.05%
OATP1B3 inhibitior + 0.9103 91.03%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9521 95.21%
P-glycoprotein inhibitior - 0.9872 98.72%
P-glycoprotein substrate - 0.8837 88.37%
CYP3A4 substrate - 0.7351 73.51%
CYP2C9 substrate - 0.8468 84.68%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.9008 90.08%
CYP2C9 inhibition - 0.9045 90.45%
CYP2C19 inhibition - 0.9432 94.32%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.5924 59.24%
CYP2C8 inhibition - 0.9909 99.09%
CYP inhibitory promiscuity - 0.9268 92.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7694 76.94%
Eye corrosion + 0.7917 79.17%
Eye irritation + 0.9661 96.61%
Skin irritation - 0.6192 61.92%
Skin corrosion - 0.9825 98.25%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6175 61.75%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6100 61.00%
skin sensitisation + 0.8792 87.92%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.9684 96.84%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.4732 47.32%
Acute Oral Toxicity (c) III 0.9159 91.59%
Estrogen receptor binding - 0.9472 94.72%
Androgen receptor binding - 0.8946 89.46%
Thyroid receptor binding - 0.7741 77.41%
Glucocorticoid receptor binding - 0.8813 88.13%
Aromatase binding - 0.8606 86.06%
PPAR gamma - 0.9061 90.61%
Honey bee toxicity - 0.9890 98.90%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.9237 92.37%
Fish aquatic toxicity + 0.6895 68.95%

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
CHEMBL2885 P07451 Carbonic anhydrase III 94.11% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.52% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.59% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.86% 97.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.55% 97.25%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.60% 92.86%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 84.40% 95.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.97% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.32% 99.17%

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.
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 13800371
NPASS NPC207998