(2R)-2-methylbutane-1,1-diol

Details

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Internal ID e295b295-79ce-4ce7-b8e1-65e276b6c70b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Carbonyl hydrates
IUPAC Name (2R)-2-methylbutane-1,1-diol
SMILES (Canonical) CCC(C)C(O)O
SMILES (Isomeric) CC[C@@H](C)C(O)O
InChI InChI=1S/C5H12O2/c1-3-4(2)5(6)7/h4-7H,3H2,1-2H3/t4-/m1/s1
InChI Key BIWVHGWGBMHTTP-SCSAIBSYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H12O2
Molecular Weight 104.15 g/mol
Exact Mass 104.083729621 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.34
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2-methylbutane-1,1-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9853 98.53%
Caco-2 + 0.5257 52.57%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5177 51.77%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.9215 92.15%
OATP1B3 inhibitior + 0.9318 93.18%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9330 93.30%
P-glycoprotein inhibitior - 0.9828 98.28%
P-glycoprotein substrate - 0.9777 97.77%
CYP3A4 substrate - 0.8111 81.11%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7565 75.65%
CYP3A4 inhibition - 0.9639 96.39%
CYP2C9 inhibition - 0.8472 84.72%
CYP2C19 inhibition - 0.9339 93.39%
CYP2D6 inhibition - 0.9321 93.21%
CYP1A2 inhibition - 0.8982 89.82%
CYP2C8 inhibition - 0.9941 99.41%
CYP inhibitory promiscuity - 0.9619 96.19%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) + 0.5958 59.58%
Carcinogenicity (trinary) Non-required 0.6332 63.32%
Eye corrosion + 0.7101 71.01%
Eye irritation + 0.7954 79.54%
Skin irritation + 0.4909 49.09%
Skin corrosion + 0.7298 72.98%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7321 73.21%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5749 57.49%
skin sensitisation - 0.5426 54.26%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6941 69.41%
Acute Oral Toxicity (c) III 0.7572 75.72%
Estrogen receptor binding - 0.9083 90.83%
Androgen receptor binding - 0.9195 91.95%
Thyroid receptor binding - 0.8338 83.38%
Glucocorticoid receptor binding - 0.9179 91.79%
Aromatase binding - 0.9228 92.28%
PPAR gamma - 0.8848 88.48%
Honey bee toxicity - 0.9752 97.52%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.9500 95.00%
Fish aquatic toxicity + 0.6549 65.49%

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 92.70% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.37% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.35% 97.25%
CHEMBL2885 P07451 Carbonic anhydrase III 84.03% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.45% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.90% 96.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.97% 85.14%

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 53684422
NPASS NPC6231