Hydroxysulfanyl hydrogen selenate

Details

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Internal ID eef9484d-46ca-443f-a95c-44499547b75d
Taxonomy Mixed metal/non-metal compounds > Other mixed metal/non-metal oxoanionic compounds > Non-metal selenates
IUPAC Name hydroxysulfanyl hydrogen selenate
SMILES (Canonical) OSO[Se](=O)(=O)O
SMILES (Isomeric) OSO[Se](=O)(=O)O
InChI InChI=1S/H2O5SSe/c1-6-5-7(2,3)4/h1H,(H,2,3,4)
InChI Key FNOLPWREOXWXTF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula H2O5SSe
Molecular Weight 193.05 g/mol
Exact Mass 193.87882 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.59
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hydroxysulfanyl hydrogen selenate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8857 88.57%
Caco-2 - 0.6617 66.17%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6309 63.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9723 97.23%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9429 94.29%
P-glycoprotein inhibitior - 0.9762 97.62%
P-glycoprotein substrate - 0.9955 99.55%
CYP3A4 substrate - 0.7063 70.63%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.8010 80.10%
CYP3A4 inhibition - 0.9727 97.27%
CYP2C9 inhibition - 0.8187 81.87%
CYP2C19 inhibition - 0.8266 82.66%
CYP2D6 inhibition - 0.9045 90.45%
CYP1A2 inhibition - 0.8427 84.27%
CYP2C8 inhibition - 0.9758 97.58%
CYP inhibitory promiscuity - 0.9365 93.65%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) + 0.5445 54.45%
Carcinogenicity (trinary) Non-required 0.6437 64.37%
Eye corrosion + 0.5321 53.21%
Eye irritation + 0.7721 77.21%
Skin irritation - 0.5504 55.04%
Skin corrosion + 0.7640 76.40%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7551 75.51%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.6902 69.02%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.7667 76.67%
Acute Oral Toxicity (c) III 0.6304 63.04%
Estrogen receptor binding - 0.8861 88.61%
Androgen receptor binding - 0.9378 93.78%
Thyroid receptor binding - 0.7559 75.59%
Glucocorticoid receptor binding - 0.8740 87.40%
Aromatase binding - 0.8177 81.77%
PPAR gamma - 0.8673 86.73%
Honey bee toxicity - 0.5000 50.00%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6255 62.55%
Fish aquatic toxicity + 0.7402 74.02%

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 80.86% 96.09%

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.
Allium ampeloprasum

Cross-Links

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PubChem 163192398
LOTUS LTS0024036
wikiData Q104998413