Thiophene-2-aldoxime

Details

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Internal ID 134e05b1-9174-423f-a395-2cd24dfc7a91
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name (NE)-N-(thiophen-2-ylmethylidene)hydroxylamine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H5NOS/c7-6-4-5-2-1-3-8-5/h1-4,7H/b6-4+
InChI Key GASLBPLHYRZLLT-GQCTYLIASA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C5H5NOS
Molecular Weight 127.17 g/mol
Exact Mass 127.00918496 g/mol
Topological Polar Surface Area (TPSA) 60.80 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Thiophene-2-aldoxime
4W6UB726D3
NSC-110538
RefChem:897898
249-778-5
29683-84-9
2-Thiophenecarboxaldehyde, oxime
Thiophene-2-Carboxaldoxime
38266-87-4
2-Thiophenealdehyde oxime
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-2-aldoxime

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9130 91.30%
Caco-2 + 0.9198 91.98%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.4284 42.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9521 95.21%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9155 91.55%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9925 99.25%
CYP3A4 substrate - 0.7773 77.73%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8084 80.84%
CYP3A4 inhibition - 0.9234 92.34%
CYP2C9 inhibition - 0.7526 75.26%
CYP2C19 inhibition + 0.5490 54.90%
CYP2D6 inhibition - 0.7960 79.60%
CYP1A2 inhibition + 0.5314 53.14%
CYP2C8 inhibition - 0.9678 96.78%
CYP inhibitory promiscuity + 0.5218 52.18%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5715 57.15%
Carcinogenicity (trinary) Non-required 0.4808 48.08%
Eye corrosion - 0.6328 63.28%
Eye irritation + 0.9963 99.63%
Skin irritation + 0.5803 58.03%
Skin corrosion - 0.7178 71.78%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7987 79.87%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.8228 82.28%
skin sensitisation + 0.5235 52.35%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7301 73.01%
Acute Oral Toxicity (c) III 0.4800 48.00%
Estrogen receptor binding - 0.9055 90.55%
Androgen receptor binding - 0.9176 91.76%
Thyroid receptor binding - 0.8549 85.49%
Glucocorticoid receptor binding - 0.8890 88.90%
Aromatase binding - 0.9120 91.20%
PPAR gamma - 0.7362 73.62%
Honey bee toxicity - 0.9642 96.42%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity - 0.5455 54.55%

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 86.27% 96.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.97% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.06% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.03% 86.33%
CHEMBL2581 P07339 Cathepsin D 81.51% 98.95%

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.
Capparis spinosa

Cross-Links

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PubChem 6876527
LOTUS LTS0232576
wikiData Q105005606