(3R)-3,8,9-trihydroxy-3-methyl-7-[(2R)-2,5,10-trihydroxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl]-2,4-dihydroanthracen-1-one

Details

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Internal ID d0fbfa27-8c8d-4116-8b78-379d5d481ca5
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name (3R)-3,8,9-trihydroxy-3-methyl-7-[(2R)-2,5,10-trihydroxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl]-2,4-dihydroanthracen-1-one
SMILES (Canonical) CC1(CC2=C(C(=O)C1)C(=C3C(=C2)C=CC(=C3O)C4=C5CC(CC(=O)C5=C(C6=C4C=CC=C6O)O)(C)O)O)O
SMILES (Isomeric) C[C@]1(CC2=C(C(=O)C1)C(=C3C(=C2)C=CC(=C3O)C4=C5C[C@@](CC(=O)C5=C(C6=C4C=CC=C6O)O)(C)O)O)O
InChI InChI=1S/C30H26O8/c1-29(37)9-14-8-13-6-7-16(26(34)22(13)27(35)21(14)19(32)11-29)23-15-4-3-5-18(31)24(15)28(36)25-17(23)10-30(2,38)12-20(25)33/h3-8,31,34-38H,9-12H2,1-2H3/t29-,30-/m1/s1
InChI Key FBPZAGOTWAVQJH-LOYHVIPDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H26O8
Molecular Weight 514.50 g/mol
Exact Mass 514.16276778 g/mol
Topological Polar Surface Area (TPSA) 156.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.24
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R)-3,8,9-trihydroxy-3-methyl-7-[(2R)-2,5,10-trihydroxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl]-2,4-dihydroanthracen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9832 98.32%
Caco-2 - 0.8071 80.71%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8093 80.93%
OATP2B1 inhibitior - 0.5619 56.19%
OATP1B1 inhibitior + 0.8582 85.82%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8741 87.41%
P-glycoprotein inhibitior - 0.4365 43.65%
P-glycoprotein substrate + 0.6060 60.60%
CYP3A4 substrate + 0.6584 65.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8222 82.22%
CYP3A4 inhibition - 0.6304 63.04%
CYP2C9 inhibition - 0.6291 62.91%
CYP2C19 inhibition - 0.7881 78.81%
CYP2D6 inhibition - 0.8309 83.09%
CYP1A2 inhibition - 0.5163 51.63%
CYP2C8 inhibition - 0.5706 57.06%
CYP inhibitory promiscuity - 0.8405 84.05%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8632 86.32%
Carcinogenicity (trinary) Non-required 0.5800 58.00%
Eye corrosion - 0.9943 99.43%
Eye irritation - 0.8222 82.22%
Skin irritation - 0.6645 66.45%
Skin corrosion - 0.8829 88.29%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7447 74.47%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.5898 58.98%
skin sensitisation - 0.8797 87.97%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.5067 50.67%
Acute Oral Toxicity (c) III 0.5826 58.26%
Estrogen receptor binding + 0.8673 86.73%
Androgen receptor binding + 0.6900 69.00%
Thyroid receptor binding + 0.5722 57.22%
Glucocorticoid receptor binding + 0.8085 80.85%
Aromatase binding + 0.6438 64.38%
PPAR gamma + 0.7901 79.01%
Honey bee toxicity - 0.9064 90.64%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9921 99.21%

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 99.70% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.64% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 98.37% 91.49%
CHEMBL1937 Q92769 Histone deacetylase 2 95.71% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.16% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.23% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.93% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.17% 99.23%
CHEMBL2535 P11166 Glucose transporter 90.15% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 89.63% 93.31%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 88.78% 81.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.60% 89.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.53% 96.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.44% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.22% 96.67%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 87.86% 85.11%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.56% 93.03%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.07% 94.00%
CHEMBL2056 P21728 Dopamine D1 receptor 86.44% 91.00%
CHEMBL4208 P20618 Proteasome component C5 84.37% 90.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.61% 100.00%

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.
Karwinskia parvifolia

Cross-Links

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PubChem 9806503
LOTUS LTS0026814
wikiData Q104992825