Xfcgmigooizcke-nscuhmnnsa-

Details

Top
Internal ID 62417168-ee35-44e7-87b3-bbb6ffbb2cd8
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name [5-[(E)-hept-5-en-1,3-diynyl]thiophen-2-yl]methanol
SMILES (Canonical) CC=CC#CC#CC1=CC=C(S1)CO
SMILES (Isomeric) C/C=C/C#CC#CC1=CC=C(S1)CO
InChI InChI=1S/C12H10OS/c1-2-3-4-5-6-7-11-8-9-12(10-13)14-11/h2-3,8-9,13H,10H2,1H3/b3-2+
InChI Key XFCGMIGOOIZCKE-NSCUHMNNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H10OS
Molecular Weight 202.27 g/mol
Exact Mass 202.04523611 g/mol
Topological Polar Surface Area (TPSA) 48.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.17
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
XFCGMIGOOIZCKE-NSCUHMNNSA-
InChI=1/C12H10OS/c1-2-3-4-5-6-7-11-8-9-12(10-13)14-11/h2-3,8-9,13H,10H2,1H3/b3-2+

2D Structure

Top
2D Structure of Xfcgmigooizcke-nscuhmnnsa-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 - 0.7333 73.33%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.3907 39.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8496 84.96%
OATP1B3 inhibitior + 0.9528 95.28%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8794 87.94%
P-glycoprotein inhibitior - 0.9749 97.49%
P-glycoprotein substrate - 0.9210 92.10%
CYP3A4 substrate - 0.6084 60.84%
CYP2C9 substrate + 0.8024 80.24%
CYP2D6 substrate - 0.8025 80.25%
CYP3A4 inhibition - 0.8823 88.23%
CYP2C9 inhibition - 0.6398 63.98%
CYP2C19 inhibition - 0.5545 55.45%
CYP2D6 inhibition - 0.8732 87.32%
CYP1A2 inhibition - 0.5496 54.96%
CYP2C8 inhibition - 0.7478 74.78%
CYP inhibitory promiscuity + 0.7323 73.23%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6917 69.17%
Carcinogenicity (trinary) Danger 0.5167 51.67%
Eye corrosion + 0.5253 52.53%
Eye irritation - 0.7640 76.40%
Skin irritation + 0.6113 61.13%
Skin corrosion - 0.5544 55.44%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7847 78.47%
Micronuclear - 0.7841 78.41%
Hepatotoxicity + 0.5303 53.03%
skin sensitisation + 0.6843 68.43%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4784 47.84%
Acute Oral Toxicity (c) III 0.6031 60.31%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.5515 55.15%
Thyroid receptor binding - 0.6353 63.53%
Glucocorticoid receptor binding + 0.5665 56.65%
Aromatase binding + 0.6474 64.74%
PPAR gamma + 0.5342 53.42%
Honey bee toxicity - 0.9173 91.73%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.7585 75.85%

Targets

Top

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
CHEMBL3492 P49721 Proteasome Macropain subunit 91.62% 90.24%
CHEMBL3401 O75469 Pregnane X receptor 89.47% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.60% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 86.38% 95.93%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 84.51% 96.42%
CHEMBL2581 P07339 Cathepsin D 81.43% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.40% 91.11%
CHEMBL2487 P05067 Beta amyloid A4 protein 81.30% 96.74%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.28% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.84% 86.33%

Plants that contains it

Top
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.
Rhaponticum carthamoides subsp. carthamoides
Xanthopappus subacaulis

Cross-Links

Top
PubChem 44583855
LOTUS LTS0103524
wikiData Q105326923