Harunmadagacarin B

Details

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Internal ID d48a3685-13fa-44d6-a5f1-6594176cb7fa
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name 6,7-dihydroxy-2,2,9-trimethyl-10,12,12-tris(3-methylbut-2-enyl)naphtho[2,3-g]chromen-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H42O4/c1-20(2)10-11-24-23(7)18-28(36)29-26(24)19-27-30(32(29)38)31(37)25-14-15-34(8,9)39-33(25)35(27,16-12-21(3)4)17-13-22(5)6/h10,12-15,18-19,36,38H,11,16-17H2,1-9H3
InChI Key KFXIGAOBONVSQG-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C35H42O4
Molecular Weight 526.70 g/mol
Exact Mass 526.30830982 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 10.00
Atomic LogP (AlogP) 8.83
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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10,12,12-Tris(3,3-dimethylallyl)-6,7-dihydroxy-2,2,9- trimethyl-1H-pyrano[2,3-b]anthracen-5(12H)-one

2D Structure

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2D Structure of Harunmadagacarin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 + 0.4939 49.39%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7214 72.14%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.7926 79.26%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9732 97.32%
P-glycoprotein inhibitior + 0.7779 77.79%
P-glycoprotein substrate - 0.5457 54.57%
CYP3A4 substrate + 0.6473 64.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8406 84.06%
CYP3A4 inhibition - 0.6978 69.78%
CYP2C9 inhibition + 0.8499 84.99%
CYP2C19 inhibition + 0.7973 79.73%
CYP2D6 inhibition - 0.7522 75.22%
CYP1A2 inhibition + 0.8666 86.66%
CYP2C8 inhibition + 0.6045 60.45%
CYP inhibitory promiscuity + 0.9012 90.12%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6229 62.29%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.5479 54.79%
Skin irritation - 0.6615 66.15%
Skin corrosion - 0.9249 92.49%
Ames mutagenesis + 0.5408 54.08%
Human Ether-a-go-go-Related Gene inhibition + 0.7768 77.68%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.5011 50.11%
skin sensitisation - 0.6622 66.22%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6082 60.82%
Acute Oral Toxicity (c) III 0.7124 71.24%
Estrogen receptor binding + 0.9272 92.72%
Androgen receptor binding + 0.6013 60.13%
Thyroid receptor binding + 0.7047 70.47%
Glucocorticoid receptor binding + 0.8777 87.77%
Aromatase binding + 0.6933 69.33%
PPAR gamma + 0.8615 86.15%
Honey bee toxicity - 0.8405 84.05%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9929 99.29%

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 99.54% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.51% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.32% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 95.58% 94.73%
CHEMBL2581 P07339 Cathepsin D 95.40% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.24% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.72% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.57% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.56% 93.40%
CHEMBL3038469 P24941 CDK2/Cyclin A 85.58% 91.38%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.64% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.99% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.73% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.11% 86.33%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.60% 96.90%
CHEMBL1937 Q92769 Histone deacetylase 2 80.44% 94.75%

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.
Harungana madagascariensis

Cross-Links

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PubChem 11329963
NPASS NPC118886
LOTUS LTS0073619
wikiData Q105140598