Streptochlorin

Details

Top
Internal ID f59b2409-51bf-41d1-854b-3d526b85d1a5
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name 4-chloro-5-(1H-indol-3-yl)-1,3-oxazole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H7ClN2O/c12-11-10(15-6-14-11)8-5-13-9-4-2-1-3-7(8)9/h1-6,13H
InChI Key BKYJGKRXUHPPLR-UHFFFAOYSA-N
Popularity 31 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H7ClN2O
Molecular Weight 218.64 g/mol
Exact Mass 218.0246905 g/mol
Topological Polar Surface Area (TPSA) 41.80 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
120191-51-7
4-Chloro-5-(1H-indol-3-yl)oxazole
SF 2583A
3-(4-chloro-5-oxazolyl)-1H-indole
SCHEMBL3797259
CHEMBL2252884
EX-A7999F
AKOS027325049
NCGC00380969-01
HY-124035
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Streptochlorin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7846 78.46%
Blood Brain Barrier + 0.8521 85.21%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6649 66.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9205 92.05%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5155 51.55%
P-glycoprotein inhibitior - 0.9478 94.78%
P-glycoprotein substrate - 0.9393 93.93%
CYP3A4 substrate + 0.5586 55.86%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.7550 75.50%
CYP3A4 inhibition - 0.7483 74.83%
CYP2C9 inhibition - 0.8838 88.38%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9288 92.88%
CYP1A2 inhibition + 0.9593 95.93%
CYP2C8 inhibition + 0.5620 56.20%
CYP inhibitory promiscuity + 0.8031 80.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6719 67.19%
Carcinogenicity (trinary) Non-required 0.6841 68.41%
Eye corrosion - 0.9865 98.65%
Eye irritation + 0.6442 64.42%
Skin irritation - 0.6916 69.16%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5603 56.03%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8733 87.33%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.6822 68.22%
Nephrotoxicity - 0.7205 72.05%
Acute Oral Toxicity (c) III 0.6909 69.09%
Estrogen receptor binding + 0.9332 93.32%
Androgen receptor binding + 0.7414 74.14%
Thyroid receptor binding + 0.7957 79.57%
Glucocorticoid receptor binding + 0.8601 86.01%
Aromatase binding + 0.9321 93.21%
PPAR gamma + 0.8009 80.09%
Honey bee toxicity - 0.8785 87.85%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity - 0.3714 37.14%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.63% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.98% 94.00%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 91.54% 89.44%
CHEMBL1951 P21397 Monoamine oxidase A 91.14% 91.49%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.47% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.40% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.93% 94.73%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 86.90% 92.67%
CHEMBL3902 P09211 Glutathione S-transferase Pi 86.26% 93.81%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 85.36% 96.39%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 84.20% 96.67%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 83.02% 93.24%
CHEMBL3310 Q96DB2 Histone deacetylase 11 82.67% 88.56%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 82.43% 83.00%
CHEMBL5543 Q9Y463 Dual specificity tyrosine-phosphorylation-regulated kinase 1B 82.06% 94.70%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 81.97% 90.71%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.10% 80.96%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.83% 100.00%
CHEMBL213 P08588 Beta-1 adrenergic receptor 80.00% 95.56%
CHEMBL1293289 P25440 Bromodomain-containing protein 2 80.00% 86.19%

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.
There are no matching plants.

Cross-Links

Top
PubChem 44608049
LOTUS LTS0185431
wikiData Q104937834