[(6S,7R,9E,11S,12R,13R,14R,15R,16R,17S,18S)-2,6,11,15,17-pentahydroxy-3,7,12,14,16,18,26-heptamethyl-23,27,29-trioxo-8,30-dioxa-24-azatetracyclo[23.3.1.14,7.05,28]triaconta-1(28),2,4,9,19,21,25-heptaen-13-yl] acetate

Details

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Internal ID 4136c0f3-d41f-4933-911d-6a5cc5f267cf
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name [(6S,7R,9E,11S,12R,13R,14R,15R,16R,17S,18S)-2,6,11,15,17-pentahydroxy-3,7,12,14,16,18,26-heptamethyl-23,27,29-trioxo-8,30-dioxa-24-azatetracyclo[23.3.1.14,7.05,28]triaconta-1(28),2,4,9,19,21,25-heptaen-13-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H45NO12/c1-15-11-9-10-12-23(40)37-27-17(3)30(43)24-25(32(27)45)31(44)20(6)34-26(24)35(46)36(8,49-34)47-14-13-22(39)16(2)33(48-21(7)38)19(5)29(42)18(4)28(15)41/h9-16,18-19,22,28-29,33,35,39,41-42,44,46H,1-8H3,(H,37,40)/b11-9?,12-10?,14-13+/t15-,16+,18+,19+,22-,28-,29+,33+,35-,36+/m0/s1
InChI Key QWIHJIQXNOWSHR-NOENESPWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H45NO12
Molecular Weight 683.70 g/mol
Exact Mass 683.29417587 g/mol
Topological Polar Surface Area (TPSA) 209.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 12
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 [(6S,7R,9E,11S,12R,13R,14R,15R,16R,17S,18S)-2,6,11,15,17-pentahydroxy-3,7,12,14,16,18,26-heptamethyl-23,27,29-trioxo-8,30-dioxa-24-azatetracyclo[23.3.1.14,7.05,28]triaconta-1(28),2,4,9,19,21,25-heptaen-13-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9555 95.55%
Caco-2 - 0.8451 84.51%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Plasma membrane 0.5221 52.21%
OATP2B1 inhibitior - 0.5210 52.10%
OATP1B1 inhibitior + 0.7661 76.61%
OATP1B3 inhibitior + 0.9233 92.33%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9483 94.83%
P-glycoprotein inhibitior - 0.4467 44.67%
P-glycoprotein substrate + 0.6619 66.19%
CYP3A4 substrate + 0.7121 71.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8941 89.41%
CYP3A4 inhibition - 0.7988 79.88%
CYP2C9 inhibition - 0.7368 73.68%
CYP2C19 inhibition - 0.7816 78.16%
CYP2D6 inhibition - 0.8566 85.66%
CYP1A2 inhibition - 0.7390 73.90%
CYP2C8 inhibition + 0.7154 71.54%
CYP inhibitory promiscuity + 0.6850 68.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Danger 0.4965 49.65%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.9132 91.32%
Skin irritation - 0.7953 79.53%
Skin corrosion - 0.9444 94.44%
Ames mutagenesis + 0.6146 61.46%
Human Ether-a-go-go-Related Gene inhibition + 0.7237 72.37%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.5574 55.74%
skin sensitisation - 0.8371 83.71%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.6177 61.77%
Acute Oral Toxicity (c) III 0.5805 58.05%
Estrogen receptor binding + 0.7837 78.37%
Androgen receptor binding + 0.7061 70.61%
Thyroid receptor binding + 0.5234 52.34%
Glucocorticoid receptor binding + 0.7633 76.33%
Aromatase binding + 0.5852 58.52%
PPAR gamma + 0.7696 76.96%
Honey bee toxicity - 0.6503 65.03%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9386 93.86%

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 98.64% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.33% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.26% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.21% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 92.78% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.86% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.57% 94.00%
CHEMBL4040 P28482 MAP kinase ERK2 88.73% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.07% 96.09%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 87.04% 89.67%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.78% 93.03%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.66% 96.77%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.19% 97.28%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.18% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.11% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.82% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.23% 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.
There are no matching plants.

Cross-Links

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PubChem 163061391
LOTUS LTS0203297
wikiData Q105229189