Isoplumbagin

Details

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Internal ID f40453c8-e68f-4537-a6bc-8157935e96ed
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 8-hydroxy-2-methylnaphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H8O3/c1-6-5-9(13)7-3-2-4-8(12)10(7)11(6)14/h2-5,12H,1H3
InChI Key ZMOIGGHUSNHCAB-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C11H8O3
Molecular Weight 188.18 g/mol
Exact Mass 188.047344113 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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14777-17-4
8-hydroxy-2-methylnaphthalene-1,4-dione
1,4-Naphthalenedione, 8-hydroxy-2-methyl-
SW8KH5YY53
2-Methyl-8-hydroxy-1,4-naphthoquinone
UNII-SW8KH5YY53
8-Hydroxy-2-methyl-1,4-naphthalenedione
2-Methyl-8-oxidanyl-naphthalene-1,4-dione
8-hydroxy-2-methyl-1,4-dihydronaphthalene-1,4-dione
Naphthsaritone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isoplumbagin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6657 66.57%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.8798 87.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9423 94.23%
OATP1B3 inhibitior + 0.9776 97.76%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9115 91.15%
P-glycoprotein inhibitior - 0.9743 97.43%
P-glycoprotein substrate - 0.9555 95.55%
CYP3A4 substrate - 0.5739 57.39%
CYP2C9 substrate - 0.8093 80.93%
CYP2D6 substrate - 0.8659 86.59%
CYP3A4 inhibition - 0.8351 83.51%
CYP2C9 inhibition + 0.8504 85.04%
CYP2C19 inhibition + 0.5513 55.13%
CYP2D6 inhibition - 0.7826 78.26%
CYP1A2 inhibition + 0.9504 95.04%
CYP2C8 inhibition - 0.9283 92.83%
CYP inhibitory promiscuity + 0.7349 73.49%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7906 79.06%
Carcinogenicity (trinary) Non-required 0.4831 48.31%
Eye corrosion - 0.9783 97.83%
Eye irritation + 0.9632 96.32%
Skin irritation + 0.7111 71.11%
Skin corrosion - 0.9239 92.39%
Ames mutagenesis + 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8705 87.05%
Micronuclear + 0.6808 68.08%
Hepatotoxicity + 0.8500 85.00%
skin sensitisation + 0.7017 70.17%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.7502 75.02%
Acute Oral Toxicity (c) II 0.7316 73.16%
Estrogen receptor binding - 0.7235 72.35%
Androgen receptor binding + 0.6489 64.89%
Thyroid receptor binding - 0.6880 68.80%
Glucocorticoid receptor binding - 0.7148 71.48%
Aromatase binding - 0.7483 74.83%
PPAR gamma - 0.6567 65.67%
Honey bee toxicity - 0.9648 96.48%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9911 99.11%

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
CHEMBL2581 P07339 Cathepsin D 97.87% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.72% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 93.27% 94.75%
CHEMBL1951 P21397 Monoamine oxidase A 92.75% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.50% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 89.47% 94.73%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 89.11% 96.67%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.31% 93.03%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.29% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.88% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.55% 93.65%

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.
Diospyros mannii
Juglans nigra
Lawsonia inermis

Cross-Links

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PubChem 375105
LOTUS LTS0163574
wikiData Q105379608