Thiophene A

Details

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Internal ID fe46a928-c751-4880-ad84-41f06caa1607
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name 2-hex-5-en-1,3-diynyl-5-prop-1-ynylthiophene
SMILES (Canonical) CC#CC1=CC=C(S1)C#CC#CC=C
SMILES (Isomeric) CC#CC1=CC=C(S1)C#CC#CC=C
InChI InChI=1S/C13H8S/c1-3-5-6-7-9-13-11-10-12(14-13)8-4-2/h3,10-11H,1H2,2H3
InChI Key CHXZRHMQQRUVHF-UHFFFAOYSA-N
Popularity 26 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8S
Molecular Weight 196.27 g/mol
Exact Mass 196.03467143 g/mol
Topological Polar Surface Area (TPSA) 28.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2134-99-8
2-hex-5-en-1,3-diynyl-5-prop-1-ynylthiophene
Y5IXF40LUG
BOHLMANN K4018
NSC-302303
2-(hexa-5-en-1,3-diyn-1-yl)-5-(prop-1-yn-1-yl)thiophene
2-(hexa-5-en-1,3-diynyl)-5-(propynyl)-thiophene
Thiophene, 2-(5-hexene-1,3-diynyl)-5-(1-propynyl)-
Thiophene-A
UNII-Y5IXF40LUG
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Thiophene A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.5602 56.02%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.4708 47.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9195 91.95%
OATP1B3 inhibitior + 0.9562 95.62%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8796 87.96%
P-glycoprotein inhibitior - 0.9511 95.11%
P-glycoprotein substrate - 0.9493 94.93%
CYP3A4 substrate - 0.6366 63.66%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8104 81.04%
CYP3A4 inhibition - 0.8756 87.56%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.5917 59.17%
CYP2D6 inhibition - 0.8194 81.94%
CYP1A2 inhibition - 0.5849 58.49%
CYP2C8 inhibition - 0.8273 82.73%
CYP inhibitory promiscuity + 0.8056 80.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6317 63.17%
Carcinogenicity (trinary) Danger 0.4188 41.88%
Eye corrosion + 0.8553 85.53%
Eye irritation + 0.6290 62.90%
Skin irritation + 0.7152 71.52%
Skin corrosion - 0.6372 63.72%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7005 70.05%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.6803 68.03%
skin sensitisation + 0.8015 80.15%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8170 81.70%
Estrogen receptor binding - 0.7934 79.34%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5917 59.17%
Glucocorticoid receptor binding + 0.6032 60.32%
Aromatase binding + 0.6596 65.96%
PPAR gamma - 0.4950 49.50%
Honey bee toxicity - 0.8809 88.09%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9790 97.90%

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
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 94.62% 96.42%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.88% 85.30%
CHEMBL1951 P21397 Monoamine oxidase A 89.08% 91.49%
CHEMBL2487 P05067 Beta amyloid A4 protein 87.69% 96.74%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.88% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.09% 98.95%
CHEMBL240 Q12809 HERG 83.09% 89.76%
CHEMBL3401 O75469 Pregnane X receptor 82.69% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.31% 95.56%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.24% 82.05%

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.
Ambrosia artemisiifolia
Ambrosia chamissonis
Blainvillea acmella
Brachylaena discolor var. transvaalensis
Centaurea cineraria subsp. cineraria
Chaenactis douglasii
Neurolaena lobata
Picradeniopsis multiflora
Pterocaulon balansae
Rudbeckia hirta
Wedelia hookeriana

Cross-Links

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PubChem 100448
NPASS NPC64849
LOTUS LTS0139821
wikiData Q83045956