Alvaradoin J

Details

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Internal ID e239918a-5a58-4fcf-bd58-e5538c2859dc
Taxonomy Benzenoids > Anthracenes
IUPAC Name [(2S,3R,4R,5R,6R)-2-acetyloxy-3,5-dihydroxy-6-[(9S)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]oxan-4-yl] 3-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H28O11/c1-11(2)8-18(31)37-24-22(33)25(38-26(23(24)34)36-13(4)28)27(35)14-6-5-7-16(29)19(14)21(32)20-15(27)9-12(3)10-17(20)30/h5-10,22-26,29-30,33-35H,1-4H3/t22-,23-,24-,25-,26-,27+/m1/s1
InChI Key CWTBVTWONZDFAF-XXVOEFFYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H28O11
Molecular Weight 528.50 g/mol
Exact Mass 528.16316171 g/mol
Topological Polar Surface Area (TPSA) 180.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Alvaradoin J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9624 96.24%
Caco-2 - 0.7761 77.61%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7195 71.95%
OATP2B1 inhibitior + 0.5741 57.41%
OATP1B1 inhibitior + 0.8852 88.52%
OATP1B3 inhibitior + 0.8347 83.47%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6215 62.15%
P-glycoprotein inhibitior + 0.6318 63.18%
P-glycoprotein substrate - 0.5558 55.58%
CYP3A4 substrate + 0.6607 66.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8780 87.80%
CYP3A4 inhibition - 0.7130 71.30%
CYP2C9 inhibition + 0.7184 71.84%
CYP2C19 inhibition + 0.6645 66.45%
CYP2D6 inhibition - 0.8974 89.74%
CYP1A2 inhibition - 0.7425 74.25%
CYP2C8 inhibition + 0.5303 53.03%
CYP inhibitory promiscuity + 0.7186 71.86%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Danger 0.4508 45.08%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.8331 83.31%
Skin irritation - 0.7438 74.38%
Skin corrosion - 0.9456 94.56%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6647 66.47%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.8016 80.16%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.6157 61.57%
Acute Oral Toxicity (c) III 0.6507 65.07%
Estrogen receptor binding + 0.6291 62.91%
Androgen receptor binding + 0.5705 57.05%
Thyroid receptor binding - 0.5198 51.98%
Glucocorticoid receptor binding + 0.6733 67.33%
Aromatase binding - 0.5309 53.09%
PPAR gamma + 0.6593 65.93%
Honey bee toxicity - 0.7531 75.31%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9948 99.48%

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 98.99% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.60% 95.56%
CHEMBL2581 P07339 Cathepsin D 96.59% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.47% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 94.91% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.10% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.35% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.21% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.23% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.30% 94.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.28% 93.40%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.41% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 85.82% 91.19%
CHEMBL1951 P21397 Monoamine oxidase A 85.26% 91.49%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 84.35% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.06% 97.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.40% 96.09%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 82.59% 97.53%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.88% 96.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.41% 100.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.34% 93.03%

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.
Alvaradoa haitiensis

Cross-Links

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PubChem 16736024
NPASS NPC177044
LOTUS LTS0077555
wikiData Q27133841