4-Methyl-3-heptanol

Details

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Internal ID 9ba9e993-d523-48dd-9e6d-95a5799a5cc0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 4-methylheptan-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H18O/c1-4-6-7(3)8(9)5-2/h7-9H,4-6H2,1-3H3
InChI Key BKQICAFAUMRYLZ-UHFFFAOYSA-N
Popularity 136 references 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) 2.19
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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14979-39-6
4-Methylheptan-3-ol
3-HEPTANOL, 4-METHYL-
DTXSID0041519
NSC-93808
L4RU749510
Caswell No. 570A
EINECS 239-058-9
NSC 93808
EPA Pesticide Chemical Code 571200
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Methyl-3-heptanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 + 0.8827 88.27%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4190 41.90%
OATP2B1 inhibitior - 0.8163 81.63%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9183 91.83%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9623 96.23%
P-glycoprotein inhibitior - 0.9785 97.85%
P-glycoprotein substrate - 0.9334 93.34%
CYP3A4 substrate - 0.7675 76.75%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.6696 66.96%
CYP3A4 inhibition - 0.9383 93.83%
CYP2C9 inhibition - 0.8675 86.75%
CYP2C19 inhibition - 0.9155 91.55%
CYP2D6 inhibition - 0.9255 92.55%
CYP1A2 inhibition + 0.5926 59.26%
CYP2C8 inhibition - 0.9956 99.56%
CYP inhibitory promiscuity - 0.8437 84.37%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7419 74.19%
Eye corrosion + 0.7963 79.63%
Eye irritation + 0.9695 96.95%
Skin irritation + 0.5221 52.21%
Skin corrosion - 0.9020 90.20%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6124 61.24%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6001 60.01%
skin sensitisation + 0.9434 94.34%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.9263 92.63%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.5522 55.22%
Acute Oral Toxicity (c) III 0.8406 84.06%
Estrogen receptor binding - 0.9248 92.48%
Androgen receptor binding - 0.8987 89.87%
Thyroid receptor binding - 0.8444 84.44%
Glucocorticoid receptor binding - 0.9220 92.20%
Aromatase binding - 0.9084 90.84%
PPAR gamma - 0.9214 92.14%
Honey bee toxicity - 0.9799 97.99%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.7539 75.39%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.48% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.21% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.90% 97.25%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.04% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 82.84% 87.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.84% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 26989
LOTUS LTS0038799
wikiData Q27282706