1-(Butan-2-yldisulfanyl)-4,4-dimethylpent-1-en-3-ol

Details

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Internal ID e6c2b220-7998-47bd-8f88-2988ad967040
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 1-(butan-2-yldisulfanyl)-4,4-dimethylpent-1-en-3-ol
SMILES (Canonical) CCC(C)SSC=CC(C(C)(C)C)O
SMILES (Isomeric) CCC(C)SSC=CC(C(C)(C)C)O
InChI InChI=1S/C11H22OS2/c1-6-9(2)14-13-8-7-10(12)11(3,4)5/h7-10,12H,6H2,1-5H3
InChI Key NHPBKKHMGJBYLO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H22OS2
Molecular Weight 234.40 g/mol
Exact Mass 234.11120767 g/mol
Topological Polar Surface Area (TPSA) 70.80 Ų
XlogP 3.50
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(Butan-2-yldisulfanyl)-4,4-dimethylpent-1-en-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9867 98.67%
Caco-2 + 0.5732 57.32%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.3652 36.52%
OATP2B1 inhibitior - 0.8627 86.27%
OATP1B1 inhibitior + 0.8804 88.04%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9321 93.21%
P-glycoprotein inhibitior - 0.9568 95.68%
P-glycoprotein substrate - 0.9078 90.78%
CYP3A4 substrate - 0.6592 65.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7607 76.07%
CYP3A4 inhibition - 0.5488 54.88%
CYP2C9 inhibition - 0.6498 64.98%
CYP2C19 inhibition - 0.6959 69.59%
CYP2D6 inhibition - 0.8717 87.17%
CYP1A2 inhibition - 0.7118 71.18%
CYP2C8 inhibition - 0.9465 94.65%
CYP inhibitory promiscuity - 0.5533 55.33%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6094 60.94%
Eye corrosion + 0.5434 54.34%
Eye irritation - 0.9117 91.17%
Skin irritation + 0.5973 59.73%
Skin corrosion - 0.6389 63.89%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6818 68.18%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5891 58.91%
skin sensitisation + 0.7422 74.22%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.6310 63.10%
Nephrotoxicity - 0.7141 71.41%
Acute Oral Toxicity (c) III 0.7495 74.95%
Estrogen receptor binding - 0.8271 82.71%
Androgen receptor binding - 0.8892 88.92%
Thyroid receptor binding + 0.5441 54.41%
Glucocorticoid receptor binding - 0.7528 75.28%
Aromatase binding - 0.8763 87.63%
PPAR gamma - 0.6467 64.67%
Honey bee toxicity - 0.8456 84.56%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity + 0.9230 92.30%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.11% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.25% 85.14%
CHEMBL2581 P07339 Cathepsin D 94.45% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.44% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.17% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.12% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.94% 93.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.32% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.20% 99.17%

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.
Ferula persica

Cross-Links

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PubChem 163192301
LOTUS LTS0053274
wikiData Q105179528