(2S)-2-methylpentan-1-ol

Details

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Internal ID 452d59be-70ea-4699-b86f-3dc0c0737ca1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name (2S)-2-methylpentan-1-ol
SMILES (Canonical) CCCC(C)CO
SMILES (Isomeric) CCC[C@H](C)CO
InChI InChI=1S/C6H14O/c1-3-4-6(2)5-7/h6-7H,3-5H2,1-2H3/t6-/m0/s1
InChI Key PFNHSEQQEPMLNI-LURJTMIESA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C6H14O
Molecular Weight 102.17 g/mol
Exact Mass 102.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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(s)-2-methyl-pentan-1-ol
(2S)-2-methyl-1-pentanol
(S)-2-Methyl-1-pentanol
SCHEMBL1203795
A801188

2D Structure

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2D Structure of (2S)-2-methylpentan-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.7697 76.97%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.6926 69.26%
OATP2B1 inhibitior - 0.8321 83.21%
OATP1B1 inhibitior + 0.9645 96.45%
OATP1B3 inhibitior + 0.9227 92.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9569 95.69%
P-glycoprotein inhibitior - 0.9881 98.81%
P-glycoprotein substrate - 0.9508 95.08%
CYP3A4 substrate - 0.7729 77.29%
CYP2C9 substrate - 0.8468 84.68%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.9295 92.95%
CYP2C9 inhibition - 0.8437 84.37%
CYP2C19 inhibition - 0.9003 90.03%
CYP2D6 inhibition - 0.8991 89.91%
CYP1A2 inhibition - 0.6179 61.79%
CYP2C8 inhibition - 0.9974 99.74%
CYP inhibitory promiscuity - 0.8206 82.06%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6586 65.86%
Eye corrosion + 0.8820 88.20%
Eye irritation + 0.9630 96.30%
Skin irritation - 0.7288 72.88%
Skin corrosion - 0.9536 95.36%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6911 69.11%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6324 63.24%
skin sensitisation + 0.9176 91.76%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5449 54.49%
Acute Oral Toxicity (c) III 0.8358 83.58%
Estrogen receptor binding - 0.9435 94.35%
Androgen receptor binding - 0.9497 94.97%
Thyroid receptor binding - 0.8758 87.58%
Glucocorticoid receptor binding - 0.9330 93.30%
Aromatase binding - 0.8857 88.57%
PPAR gamma - 0.9306 93.06%
Honey bee toxicity - 0.9922 99.22%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.8934 89.34%
Fish aquatic toxicity + 0.7978 79.78%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.95% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.15% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 88.33% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.61% 97.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.52% 97.25%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 81.62% 95.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.65% 93.56%

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.
Patrinia scabiosifolia
Patrinia villosa

Cross-Links

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PubChem 6999993
NPASS NPC291024