Xanthopappin A

Details

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Internal ID 674f6ac7-b340-491b-ba0d-8f17293af29c
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-[(E)-hept-5-en-1,3-diynyl]thiophene
SMILES (Canonical) CC=CC#CC#CC1=CC=CS1
SMILES (Isomeric) C/C=C/C#CC#CC1=CC=CS1
InChI InChI=1S/C11H8S/c1-2-3-4-5-6-8-11-9-7-10-12-11/h2-3,7,9-10H,1H3/b3-2+
InChI Key VDPJXBAVKXXKLA-NSCUHMNNSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H8S
Molecular Weight 172.25 g/mol
Exact Mass 172.03467143 g/mol
Topological Polar Surface Area (TPSA) 28.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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CHEMBL453761
2-[(E)-hept-5-en-1,3-diynyl]thiophene

2D Structure

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2D Structure of Xanthopappin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.6813 68.13%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4537 45.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8897 88.97%
OATP1B3 inhibitior + 0.9586 95.86%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8844 88.44%
P-glycoprotein inhibitior - 0.9782 97.82%
P-glycoprotein substrate - 0.9487 94.87%
CYP3A4 substrate - 0.6462 64.62%
CYP2C9 substrate + 0.8110 81.10%
CYP2D6 substrate - 0.8058 80.58%
CYP3A4 inhibition - 0.9329 93.29%
CYP2C9 inhibition + 0.5641 56.41%
CYP2C19 inhibition + 0.5883 58.83%
CYP2D6 inhibition - 0.8023 80.23%
CYP1A2 inhibition - 0.5552 55.52%
CYP2C8 inhibition - 0.8528 85.28%
CYP inhibitory promiscuity + 0.8403 84.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6217 62.17%
Carcinogenicity (trinary) Danger 0.4936 49.36%
Eye corrosion + 0.8634 86.34%
Eye irritation + 0.8135 81.35%
Skin irritation + 0.7757 77.57%
Skin corrosion - 0.5609 56.09%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7385 73.85%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5891 58.91%
skin sensitisation + 0.8122 81.22%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.5937 59.37%
Acute Oral Toxicity (c) III 0.8363 83.63%
Estrogen receptor binding - 0.5441 54.41%
Androgen receptor binding - 0.7718 77.18%
Thyroid receptor binding - 0.6861 68.61%
Glucocorticoid receptor binding - 0.5155 51.55%
Aromatase binding + 0.5659 56.59%
PPAR gamma - 0.5877 58.77%
Honey bee toxicity - 0.9015 90.15%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.9539 95.39%

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 95.08% 96.42%
CHEMBL2581 P07339 Cathepsin D 86.14% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.04% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 84.51% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.30% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.07% 86.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.54% 90.24%

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.
Xanthopappus subacaulis

Cross-Links

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PubChem 16083186
LOTUS LTS0073744
wikiData Q105284314