5-Epi-asperdichrome

Details

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Internal ID b58a2d80-8e86-491b-a8b9-a04bc33cde62
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthenes
IUPAC Name methyl (3S,4R,4aR)-7-[[(5R,6S,10aR)-5,9-dihydroxy-10a-methoxycarbonyl-6-methyl-8-oxo-6,7-dihydro-5H-xanthen-1-yl]oxy]-4,8,9-trihydroxy-3-methyl-1-oxo-3,4-dihydro-2H-xanthene-4a-carboxylate
SMILES (Canonical) CC1CC(=O)C2=C(C3=C(C=CC=C3OC4=C(C5=C(C=C4)OC6(C(C(CC(=O)C6=C5O)C)O)C(=O)OC)O)OC2(C1O)C(=O)OC)O
SMILES (Isomeric) C[C@H]1CC(=O)C2=C(C3=C(C=CC=C3OC4=C(C5=C(C=C4)O[C@]6([C@@H]([C@H](CC(=O)C6=C5O)C)O)C(=O)OC)O)O[C@]2([C@@H]1O)C(=O)OC)O
InChI InChI=1S/C32H30O14/c1-12-10-14(33)22-25(36)20-16(6-5-7-17(20)45-31(22,27(12)38)29(40)42-3)44-19-9-8-18-21(24(19)35)26(37)23-15(34)11-13(2)28(39)32(23,46-18)30(41)43-4/h5-9,12-13,27-28,35-39H,10-11H2,1-4H3/t12-,13-,27+,28+,31+,32+/m0/s1
InChI Key ZWKHHTDRHMFWDL-NKGGJOAPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C32H30O14
Molecular Weight 638.60 g/mol
Exact Mass 638.16355563 g/mol
Topological Polar Surface Area (TPSA) 216.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.27
H-Bond Acceptor 14
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 5-Epi-asperdichrome

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9229 92.29%
Caco-2 - 0.8461 84.61%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5408 54.08%
OATP2B1 inhibitior + 0.5689 56.89%
OATP1B1 inhibitior + 0.9070 90.70%
OATP1B3 inhibitior + 0.8877 88.77%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9571 95.71%
P-glycoprotein inhibitior + 0.7427 74.27%
P-glycoprotein substrate - 0.5286 52.86%
CYP3A4 substrate + 0.6631 66.31%
CYP2C9 substrate - 0.6017 60.17%
CYP2D6 substrate - 0.8531 85.31%
CYP3A4 inhibition - 0.7880 78.80%
CYP2C9 inhibition - 0.7318 73.18%
CYP2C19 inhibition - 0.7528 75.28%
CYP2D6 inhibition - 0.8154 81.54%
CYP1A2 inhibition - 0.7441 74.41%
CYP2C8 inhibition + 0.5510 55.10%
CYP inhibitory promiscuity - 0.7057 70.57%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.5064 50.64%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.8979 89.79%
Skin irritation - 0.7206 72.06%
Skin corrosion - 0.9340 93.40%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7739 77.39%
Micronuclear + 0.6700 67.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8240 82.40%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.5632 56.32%
Acute Oral Toxicity (c) I 0.7011 70.11%
Estrogen receptor binding + 0.7972 79.72%
Androgen receptor binding + 0.7337 73.37%
Thyroid receptor binding + 0.6260 62.60%
Glucocorticoid receptor binding + 0.7452 74.52%
Aromatase binding + 0.6538 65.38%
PPAR gamma + 0.6755 67.55%
Honey bee toxicity - 0.8050 80.50%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9802 98.02%

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 97.63% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.18% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.58% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.56% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.64% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.41% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.53% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.13% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 88.34% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.48% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.97% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.20% 95.89%
CHEMBL5028 O14672 ADAM10 82.66% 97.50%
CHEMBL4040 P28482 MAP kinase ERK2 82.41% 83.82%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.30% 94.80%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.76% 90.71%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.46% 97.14%

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 139590722
LOTUS LTS0180740
wikiData Q105384991