Seriniquinone

Details

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Internal ID 2696946a-1215-417f-8364-c2163f2aa1e3
Taxonomy Benzenoids > Naphthalenes > Naphthothiophenes
IUPAC Name 12-thiapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(13),2(11),4,6,8,15,17,19-octaene-3,10,14,21-tetrone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H8O4S/c21-15-9-5-1-3-7-11(9)17(23)19-13(15)14-16(22)10-6-2-4-8-12(10)18(24)20(14)25-19/h1-8H
InChI Key PWUWIMAXHCTYJA-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C20H8O4S
Molecular Weight 344.30 g/mol
Exact Mass 344.01432991 g/mol
Topological Polar Surface Area (TPSA) 96.50 Ų
XlogP 4.20
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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22200-69-7
12-thiapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(13),2(11),4,6,8,15,17,19-octaene-3,10,14,21-tetrone
12-thiapentacyclo(11.8.0.02,11.04,9.015,20)henicosa-1(13),2(11),4,6,8,15,17,19-octaene-3,10,14,21-tetrone
RefChem:182516
Dinaphtho[2,3-b;2',3'-d]thiophene-5,7,12,13-tetraone
orb1702812
CHEMBL4438542
SCHEMBL15551462
SCHEMBL29906291
CHEBI:215683
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Seriniquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.6403 64.03%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.6344 63.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9743 97.43%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.5577 55.77%
P-glycoprotein inhibitior - 0.7814 78.14%
P-glycoprotein substrate - 0.9793 97.93%
CYP3A4 substrate - 0.6587 65.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8107 81.07%
CYP3A4 inhibition + 0.5196 51.96%
CYP2C9 inhibition + 0.5367 53.67%
CYP2C19 inhibition + 0.5339 53.39%
CYP2D6 inhibition - 0.7633 76.33%
CYP1A2 inhibition + 0.8914 89.14%
CYP2C8 inhibition - 0.9473 94.73%
CYP inhibitory promiscuity + 0.5784 57.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8485 84.85%
Carcinogenicity (trinary) Warning 0.4282 42.82%
Eye corrosion - 0.9682 96.82%
Eye irritation + 0.7740 77.40%
Skin irritation - 0.6191 61.91%
Skin corrosion - 0.9724 97.24%
Ames mutagenesis + 0.6991 69.91%
Human Ether-a-go-go-Related Gene inhibition - 0.7221 72.21%
Micronuclear + 0.6907 69.07%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation - 0.7273 72.73%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6228 62.28%
Acute Oral Toxicity (c) III 0.6843 68.43%
Estrogen receptor binding + 0.7327 73.27%
Androgen receptor binding + 0.7065 70.65%
Thyroid receptor binding - 0.6966 69.66%
Glucocorticoid receptor binding + 0.6319 63.19%
Aromatase binding - 0.5091 50.91%
PPAR gamma - 0.6096 60.96%
Honey bee toxicity - 0.8943 89.43%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.9831 98.31%

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
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 96.95% 85.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.71% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.89% 91.11%
CHEMBL2581 P07339 Cathepsin D 87.04% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.98% 99.23%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 83.21% 92.67%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.50% 93.99%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 15154132
LOTUS LTS0014219
wikiData Q77563204