2,3-Dimethylbutan-1-ol

Details

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Internal ID 6801a33c-2219-4558-b4db-ee9c4e025626
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name 2,3-dimethylbutan-1-ol
SMILES (Canonical) CC(C)C(C)CO
SMILES (Isomeric) CC(C)C(C)CO
InChI InChI=1S/C6H14O/c1-5(2)6(3)4-7/h5-7H,4H2,1-3H3
InChI Key SXSWMAUXEHKFGX-UHFFFAOYSA-N
Popularity 22 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 1.70
Atomic LogP (AlogP) 1.27
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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19550-30-2
2,3-DIMETHYL-1-BUTANOL
DIMETHYLBUTANOL
1-Butanol, 2,3-dimethyl-
2,3-DIMETHYLBUTANOL
EINECS 243-153-0
20281-85-0
54206-54-1
79956-98-2
2,3-methylbutanol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3-Dimethylbutan-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 + 0.9900 99.00%
Caco-2 + 0.5366 53.66%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.6432 64.32%
OATP2B1 inhibitior - 0.8634 86.34%
OATP1B1 inhibitior + 0.9567 95.67%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9239 92.39%
P-glycoprotein inhibitior - 0.9843 98.43%
P-glycoprotein substrate - 0.9774 97.74%
CYP3A4 substrate - 0.8096 80.96%
CYP2C9 substrate - 0.8169 81.69%
CYP2D6 substrate - 0.7784 77.84%
CYP3A4 inhibition - 0.9661 96.61%
CYP2C9 inhibition - 0.9600 96.00%
CYP2C19 inhibition - 0.9424 94.24%
CYP2D6 inhibition - 0.9471 94.71%
CYP1A2 inhibition - 0.8454 84.54%
CYP2C8 inhibition - 0.9987 99.87%
CYP inhibitory promiscuity - 0.9618 96.18%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.5083 50.83%
Carcinogenicity (trinary) Non-required 0.7075 70.75%
Eye corrosion + 0.9867 98.67%
Eye irritation + 0.9685 96.85%
Skin irritation + 0.8523 85.23%
Skin corrosion - 0.7226 72.26%
Ames mutagenesis - 0.9583 95.83%
Human Ether-a-go-go-Related Gene inhibition - 0.7219 72.19%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5443 54.43%
skin sensitisation - 0.5474 54.74%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5416 54.16%
Acute Oral Toxicity (c) III 0.8865 88.65%
Estrogen receptor binding - 0.9400 94.00%
Androgen receptor binding - 0.8855 88.55%
Thyroid receptor binding - 0.8601 86.01%
Glucocorticoid receptor binding - 0.9249 92.49%
Aromatase binding - 0.9146 91.46%
PPAR gamma - 0.9210 92.10%
Honey bee toxicity - 0.9687 96.87%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.5237 52.37%

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 90.62% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 85.68% 87.45%
CHEMBL2581 P07339 Cathepsin D 85.23% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.45% 97.25%

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 29656
NPASS NPC121664