Altertoxin IV(Racemic Mixture)

Details

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Internal ID d901a92e-6282-46e4-8ccc-29ad2cf5cbf6
Taxonomy Benzenoids > Phenanthrenes and derivatives
IUPAC Name 4,14-dioxaheptacyclo[10.8.1.12,7.03,5.013,15.017,21.011,22]docosa-1(21),7,9,11(22),17,19-hexaene-6,8,16,18-tetrol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H16O6/c21-7-3-1-5-9-12(18-20(26-18)15(23)13(7)9)6-2-4-8(22)14-10(6)11(5)17-19(25-17)16(14)24/h1-4,11-12,15-24H
InChI Key XSDHEAABYNNUIQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H16O6
Molecular Weight 352.30 g/mol
Exact Mass 352.09468823 g/mol
Topological Polar Surface Area (TPSA) 106.00 Ų
XlogP 0.10
Atomic LogP (AlogP) 1.30
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Altertoxin IV(Racemic Mixture)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9475 94.75%
Caco-2 - 0.7451 74.51%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4361 43.61%
OATP2B1 inhibitior - 0.7102 71.02%
OATP1B1 inhibitior + 0.9425 94.25%
OATP1B3 inhibitior + 0.8987 89.87%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8169 81.69%
P-glycoprotein inhibitior - 0.7462 74.62%
P-glycoprotein substrate - 0.9483 94.83%
CYP3A4 substrate - 0.6338 63.38%
CYP2C9 substrate - 0.5885 58.85%
CYP2D6 substrate + 0.3503 35.03%
CYP3A4 inhibition - 0.6116 61.16%
CYP2C9 inhibition - 0.5942 59.42%
CYP2C19 inhibition - 0.5279 52.79%
CYP2D6 inhibition - 0.8044 80.44%
CYP1A2 inhibition + 0.6266 62.66%
CYP2C8 inhibition - 0.7200 72.00%
CYP inhibitory promiscuity + 0.5239 52.39%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5909 59.09%
Eye corrosion - 0.9832 98.32%
Eye irritation + 0.6455 64.55%
Skin irritation + 0.5924 59.24%
Skin corrosion - 0.9292 92.92%
Ames mutagenesis + 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6877 68.77%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.6128 61.28%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5972 59.72%
Acute Oral Toxicity (c) III 0.5008 50.08%
Estrogen receptor binding - 0.5183 51.83%
Androgen receptor binding + 0.6685 66.85%
Thyroid receptor binding + 0.7088 70.88%
Glucocorticoid receptor binding + 0.6319 63.19%
Aromatase binding - 0.4931 49.31%
PPAR gamma + 0.7586 75.86%
Honey bee toxicity - 0.9290 92.90%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.8388 83.88%

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 95.88% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.56% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 87.31% 91.49%
CHEMBL4040 P28482 MAP kinase ERK2 82.74% 83.82%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.37% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 81.41% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.25% 96.09%

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 162922296
LOTUS LTS0060988
wikiData Q104201297