N-(2-hydroxy-3-methylbutyl)-3-methylbutanamide

Details

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Internal ID bd81fa4f-7e78-41a9-9f72-bd99f4d15a3c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name N-(2-hydroxy-3-methylbutyl)-3-methylbutanamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H21NO2/c1-7(2)5-10(13)11-6-9(12)8(3)4/h7-9,12H,5-6H2,1-4H3,(H,11,13)
InChI Key YCKYNSJEWUMKBY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H21NO2
Molecular Weight 187.28 g/mol
Exact Mass 187.157228913 g/mol
Topological Polar Surface Area (TPSA) 49.30 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.17
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N-(2-hydroxy-3-methylbutyl)-3-methylbutanamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9832 98.32%
Caco-2 + 0.7420 74.20%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6826 68.26%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9476 94.76%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9475 94.75%
P-glycoprotein inhibitior - 0.9616 96.16%
P-glycoprotein substrate - 0.8864 88.64%
CYP3A4 substrate - 0.6536 65.36%
CYP2C9 substrate - 0.5862 58.62%
CYP2D6 substrate - 0.8227 82.27%
CYP3A4 inhibition - 0.9653 96.53%
CYP2C9 inhibition - 0.9094 90.94%
CYP2C19 inhibition - 0.8407 84.07%
CYP2D6 inhibition - 0.8488 84.88%
CYP1A2 inhibition - 0.7923 79.23%
CYP2C8 inhibition - 0.9969 99.69%
CYP inhibitory promiscuity - 0.9514 95.14%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.7011 70.11%
Eye corrosion - 0.8298 82.98%
Eye irritation - 0.6700 67.00%
Skin irritation - 0.8027 80.27%
Skin corrosion - 0.9060 90.60%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7713 77.13%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5303 53.03%
skin sensitisation - 0.9403 94.03%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.5799 57.99%
Acute Oral Toxicity (c) III 0.6855 68.55%
Estrogen receptor binding - 0.8839 88.39%
Androgen receptor binding - 0.8815 88.15%
Thyroid receptor binding - 0.7529 75.29%
Glucocorticoid receptor binding - 0.7899 78.99%
Aromatase binding - 0.8206 82.06%
PPAR gamma - 0.9007 90.07%
Honey bee toxicity - 0.9654 96.54%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.8997 89.97%

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 96.76% 83.82%
CHEMBL2581 P07339 Cathepsin D 96.61% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.11% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.33% 97.29%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 88.80% 89.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 87.46% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.25% 85.14%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.47% 96.47%
CHEMBL3401 O75469 Pregnane X receptor 81.16% 94.73%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 81.02% 96.67%

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.
Garcinia scortechinii

Cross-Links

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PubChem 115701638
LOTUS LTS0061510
wikiData Q105031055