(2S)-2-chloro-4-(5-penta-1,3-diynylthiophen-2-yl)but-3-yn-1-ol

Details

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Internal ID fb04254c-5ea0-4440-8acd-304263eb9650
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name (2S)-2-chloro-4-(5-penta-1,3-diynylthiophen-2-yl)but-3-yn-1-ol
SMILES (Canonical) CC#CC#CC1=CC=C(S1)C#CC(CO)Cl
SMILES (Isomeric) CC#CC#CC1=CC=C(S1)C#C[C@@H](CO)Cl
InChI InChI=1S/C13H9ClOS/c1-2-3-4-5-12-8-9-13(16-12)7-6-11(14)10-15/h8-9,11,15H,10H2,1H3/t11-/m0/s1
InChI Key OIMRGFPTZIUKNX-NSHDSACASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H9ClOS
Molecular Weight 248.73 g/mol
Exact Mass 248.0062638 g/mol
Topological Polar Surface Area (TPSA) 48.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2-chloro-4-(5-penta-1,3-diynylthiophen-2-yl)but-3-yn-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 + 0.9925 99.25%
Caco-2 - 0.7764 77.64%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4747 47.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9393 93.93%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6841 68.41%
P-glycoprotein inhibitior - 0.9689 96.89%
P-glycoprotein substrate - 0.9122 91.22%
CYP3A4 substrate - 0.5785 57.85%
CYP2C9 substrate - 0.7985 79.85%
CYP2D6 substrate - 0.7981 79.81%
CYP3A4 inhibition - 0.8205 82.05%
CYP2C9 inhibition + 0.5214 52.14%
CYP2C19 inhibition + 0.6734 67.34%
CYP2D6 inhibition - 0.8269 82.69%
CYP1A2 inhibition + 0.5594 55.94%
CYP2C8 inhibition - 0.8906 89.06%
CYP inhibitory promiscuity + 0.6029 60.29%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5929 59.29%
Carcinogenicity (trinary) Danger 0.5414 54.14%
Eye corrosion + 0.6120 61.20%
Eye irritation - 0.9169 91.69%
Skin irritation + 0.5602 56.02%
Skin corrosion - 0.5069 50.69%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6196 61.96%
Micronuclear - 0.8041 80.41%
Hepatotoxicity + 0.5770 57.70%
skin sensitisation + 0.5681 56.81%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.5828 58.28%
Acute Oral Toxicity (c) II 0.5496 54.96%
Estrogen receptor binding + 0.6402 64.02%
Androgen receptor binding + 0.5837 58.37%
Thyroid receptor binding - 0.4917 49.17%
Glucocorticoid receptor binding + 0.6362 63.62%
Aromatase binding + 0.6469 64.69%
PPAR gamma + 0.6110 61.10%
Honey bee toxicity - 0.8823 88.23%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5802 58.02%
Fish aquatic toxicity + 0.7329 73.29%

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 92.18% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.41% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.33% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.14% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.23% 86.92%

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.
Pluchea dioscoridis

Cross-Links

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PubChem 162921304
LOTUS LTS0015716
wikiData Q105192606