3-Methyl-2-prenylthiophene

Details

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Internal ID 6819729c-1f2f-40c0-b06d-b0dfe651abd2
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 3-methyl-2-(3-methylbut-2-enyl)thiophene
SMILES (Canonical) CC1=C(SC=C1)CC=C(C)C
SMILES (Isomeric) CC1=C(SC=C1)CC=C(C)C
InChI InChI=1S/C10H14S/c1-8(2)4-5-10-9(3)6-7-11-10/h4,6-7H,5H2,1-3H3
InChI Key CVIDZLCXVGUFAC-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H14S
Molecular Weight 166.29 g/mol
Exact Mass 166.08162162 g/mol
Topological Polar Surface Area (TPSA) 28.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.57
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Methyl-2-prenylthiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.8432 84.32%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Nucleus 0.3443 34.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9587 95.87%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8414 84.14%
P-glycoprotein inhibitior - 0.9787 97.87%
P-glycoprotein substrate - 0.9461 94.61%
CYP3A4 substrate - 0.6977 69.77%
CYP2C9 substrate - 0.6131 61.31%
CYP2D6 substrate - 0.7027 70.27%
CYP3A4 inhibition - 0.9302 93.02%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.5802 58.02%
CYP2D6 inhibition - 0.7631 76.31%
CYP1A2 inhibition + 0.5681 56.81%
CYP2C8 inhibition - 0.9259 92.59%
CYP inhibitory promiscuity + 0.9359 93.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.4276 42.76%
Eye corrosion - 0.7906 79.06%
Eye irritation + 0.9545 95.45%
Skin irritation + 0.5548 55.48%
Skin corrosion - 0.8021 80.21%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5528 55.28%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8198 81.98%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7541 75.41%
Acute Oral Toxicity (c) III 0.7329 73.29%
Estrogen receptor binding - 0.9126 91.26%
Androgen receptor binding - 0.8909 89.09%
Thyroid receptor binding - 0.9117 91.17%
Glucocorticoid receptor binding - 0.8577 85.77%
Aromatase binding - 0.5530 55.30%
PPAR gamma - 0.8227 82.27%
Honey bee toxicity - 0.9714 97.14%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9951 99.51%

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
CHEMBL3401 O75469 Pregnane X receptor 90.76% 94.73%
CHEMBL2581 P07339 Cathepsin D 89.20% 98.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.77% 90.24%
CHEMBL221 P23219 Cyclooxygenase-1 83.92% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.68% 96.09%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.57% 96.90%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.08% 96.00%

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.
Rosa canina

Cross-Links

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PubChem 10942818
LOTUS LTS0045866
wikiData Q104970756