2,3-Dimethylpentane, (S)-

Details

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Internal ID 38566aaf-064d-41cb-ae36-b3b55ef0737b
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name (3S)-2,3-dimethylpentane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H16/c1-5-7(4)6(2)3/h6-7H,5H2,1-4H3/t7-/m0/s1
InChI Key WGECXQBGLLYSFP-ZETCQYMHSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C7H16
Molecular Weight 100.20 g/mol
Exact Mass 100.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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KAA3S74KJD
2,3-Dimethylpentane, (S)-
7485-45-2
RefChem:1059489
(-)-2,3-Dimethylpentane
(3S)-2,3-Dimethylpentane
Pentane, 2,3-dimethyl-, (S)-
Pentane, 2,3-dimethyl-, (3S)-
UNII-KAA3S74KJD
Pentane, 2,3-dimethyl-, (3S)-(-)-
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-Dimethylpentane, (S)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.6563 65.63%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.4994 49.94%
OATP2B1 inhibitior - 0.8625 86.25%
OATP1B1 inhibitior + 0.9379 93.79%
OATP1B3 inhibitior + 0.9502 95.02%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9387 93.87%
P-glycoprotein inhibitior - 0.9812 98.12%
P-glycoprotein substrate - 0.9685 96.85%
CYP3A4 substrate - 0.8218 82.18%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9819 98.19%
CYP2C9 inhibition - 0.9346 93.46%
CYP2C19 inhibition - 0.9590 95.90%
CYP2D6 inhibition - 0.9254 92.54%
CYP1A2 inhibition - 0.8390 83.90%
CYP2C8 inhibition - 0.9955 99.55%
CYP inhibitory promiscuity - 0.8784 87.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.5352 53.52%
Eye corrosion + 0.9918 99.18%
Eye irritation + 0.9919 99.19%
Skin irritation + 0.8624 86.24%
Skin corrosion - 0.9544 95.44%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7561 75.61%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7590 75.90%
skin sensitisation + 0.8839 88.39%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity + 1.0000 100.00%
Nephrotoxicity + 0.4943 49.43%
Acute Oral Toxicity (c) III 0.5749 57.49%
Estrogen receptor binding - 0.9090 90.90%
Androgen receptor binding - 0.9016 90.16%
Thyroid receptor binding - 0.8640 86.40%
Glucocorticoid receptor binding - 0.9301 93.01%
Aromatase binding - 0.8685 86.85%
PPAR gamma - 0.9041 90.41%
Honey bee toxicity - 0.9458 94.58%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9077 90.77%

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
CHEMBL2581 P07339 Cathepsin D 89.65% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.38% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.47% 97.25%
CHEMBL2885 P07451 Carbonic anhydrase III 80.61% 87.45%

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.
Glycyrrhiza

Cross-Links

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PubChem 22810194
NPASS NPC238164