7-epi-8-hydroxyaltertoxin I

Details

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Internal ID 7d9c2fa3-2b53-4bf8-986a-fa0e90a1f15a
Taxonomy Benzenoids > Perylenequinones
IUPAC Name (11R,12R,12aR,12bS)-4,9,11,12,12b-pentahydroxy-2,11,12,12a-tetrahydro-1H-perylene-3,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H16O7/c21-9-4-2-8-7-1-3-10(22)14-12(7)16(18(25)19(26)17(14)24)20(27)6-5-11(23)13(9)15(8)20/h1-4,16,18-19,21-22,25-27H,5-6H2/t16-,18-,19+,20-/m1/s1
InChI Key WUCMTTYUUQBEMP-RSPOEFSDSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H16O7
Molecular Weight 368.30 g/mol
Exact Mass 368.08960285 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-epi-8-hydroxyaltertoxin I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8993 89.93%
Caco-2 - 0.8662 86.62%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6420 64.20%
OATP2B1 inhibitior - 0.6966 69.66%
OATP1B1 inhibitior + 0.9480 94.80%
OATP1B3 inhibitior + 0.9645 96.45%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9071 90.71%
BSEP inhibitior - 0.7731 77.31%
P-glycoprotein inhibitior - 0.8985 89.85%
P-glycoprotein substrate - 0.7736 77.36%
CYP3A4 substrate + 0.5804 58.04%
CYP2C9 substrate - 0.5981 59.81%
CYP2D6 substrate - 0.8122 81.22%
CYP3A4 inhibition - 0.8149 81.49%
CYP2C9 inhibition - 0.8498 84.98%
CYP2C19 inhibition - 0.8757 87.57%
CYP2D6 inhibition - 0.8879 88.79%
CYP1A2 inhibition - 0.6622 66.22%
CYP2C8 inhibition - 0.8198 81.98%
CYP inhibitory promiscuity - 0.9700 97.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9111 91.11%
Carcinogenicity (trinary) Non-required 0.5038 50.38%
Eye corrosion - 0.9921 99.21%
Eye irritation + 0.5263 52.63%
Skin irritation - 0.5541 55.41%
Skin corrosion - 0.8344 83.44%
Ames mutagenesis + 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7838 78.38%
Micronuclear - 0.5041 50.41%
Hepatotoxicity - 0.5541 55.41%
skin sensitisation - 0.7100 71.00%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.7757 77.57%
Acute Oral Toxicity (c) III 0.6806 68.06%
Estrogen receptor binding + 0.6862 68.62%
Androgen receptor binding + 0.6368 63.68%
Thyroid receptor binding - 0.6641 66.41%
Glucocorticoid receptor binding + 0.8055 80.55%
Aromatase binding - 0.5698 56.98%
PPAR gamma + 0.7637 76.37%
Honey bee toxicity - 0.8798 87.98%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9093 90.93%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.94% 91.11%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 97.66% 96.38%
CHEMBL2581 P07339 Cathepsin D 93.48% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.53% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.23% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.87% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.57% 100.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.45% 93.40%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.26% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.93% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.64% 99.15%
CHEMBL1929 P47989 Xanthine dehydrogenase 84.59% 96.12%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.58% 95.89%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.22% 93.03%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.11% 93.04%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.01% 90.71%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 82.72% 85.11%
CHEMBL2535 P11166 Glucose transporter 81.81% 98.75%

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 139585408
LOTUS LTS0219477
wikiData Q77421662