[(1S,2R,3R,4R,7S,10S,12S,14S,15S,17R,19S,20R)-15-(furan-3-yl)-3,10,20-trihydroxy-2,7,14,20-tetramethyl-5,13-dioxo-6,11,18-trioxahexacyclo[10.8.0.02,10.03,7.014,19.017,19]icos-8-en-4-yl] acetate

Details

Top
Internal ID 8d0a230e-e91f-4c4b-9db2-9c3fc09b4e18
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name [(1S,2R,3R,4R,7S,10S,12S,14S,15S,17R,19S,20R)-15-(furan-3-yl)-3,10,20-trihydroxy-2,7,14,20-tetramethyl-5,13-dioxo-6,11,18-trioxahexacyclo[10.8.0.02,10.03,7.014,19.017,19]icos-8-en-4-yl] acetate
SMILES (Canonical) CC(=O)OC1C(=O)OC2(C1(C3(C4C(C(=O)C5(C(CC6C5(C4(C)O)O6)C7=COC=C7)C)OC3(C=C2)O)C)O)C
SMILES (Isomeric) CC(=O)O[C@H]1C(=O)O[C@@]2([C@]1([C@]3([C@H]4[C@@H](C(=O)[C@]5([C@@H](C[C@@H]6[C@@]5([C@]4(C)O)O6)C7=COC=C7)C)O[C@]3(C=C2)O)C)O)C
InChI InChI=1S/C27H30O11/c1-12(28)35-19-20(30)38-21(2)7-8-25(32)23(4,26(19,21)33)17-16(37-25)18(29)22(3)14(13-6-9-34-11-13)10-15-27(22,36-15)24(17,5)31/h6-9,11,14-17,19,31-33H,10H2,1-5H3/t14-,15+,16-,17+,19-,21-,22+,23-,24+,25-,26+,27+/m0/s1
InChI Key GRNZBGWUEOICKI-ABIJRLSZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C27H30O11
Molecular Weight 530.50 g/mol
Exact Mass 530.17881177 g/mol
Topological Polar Surface Area (TPSA) 165.00 Ų
XlogP -0.60
Atomic LogP (AlogP) 0.50
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [(1S,2R,3R,4R,7S,10S,12S,14S,15S,17R,19S,20R)-15-(furan-3-yl)-3,10,20-trihydroxy-2,7,14,20-tetramethyl-5,13-dioxo-6,11,18-trioxahexacyclo[10.8.0.02,10.03,7.014,19.017,19]icos-8-en-4-yl] acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8964 89.64%
Caco-2 - 0.7777 77.77%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6452 64.52%
OATP2B1 inhibitior - 0.7173 71.73%
OATP1B1 inhibitior + 0.7303 73.03%
OATP1B3 inhibitior + 0.8548 85.48%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8992 89.92%
P-glycoprotein inhibitior + 0.6610 66.10%
P-glycoprotein substrate + 0.6251 62.51%
CYP3A4 substrate + 0.7138 71.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8656 86.56%
CYP3A4 inhibition + 0.6901 69.01%
CYP2C9 inhibition - 0.8350 83.50%
CYP2C19 inhibition - 0.8722 87.22%
CYP2D6 inhibition - 0.9165 91.65%
CYP1A2 inhibition - 0.9014 90.14%
CYP2C8 inhibition + 0.5861 58.61%
CYP inhibitory promiscuity - 0.6444 64.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Danger 0.5141 51.41%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.8938 89.38%
Skin irritation - 0.6930 69.30%
Skin corrosion - 0.8937 89.37%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4268 42.68%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8250 82.50%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.6968 69.68%
Acute Oral Toxicity (c) I 0.4705 47.05%
Estrogen receptor binding + 0.8053 80.53%
Androgen receptor binding + 0.7417 74.17%
Thyroid receptor binding + 0.6721 67.21%
Glucocorticoid receptor binding + 0.7509 75.09%
Aromatase binding + 0.6812 68.12%
PPAR gamma + 0.6418 64.18%
Honey bee toxicity - 0.6975 69.75%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9558 95.58%

Targets

Top

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 98.75% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.45% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.49% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.30% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.57% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.04% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.81% 97.09%
CHEMBL2581 P07339 Cathepsin D 88.18% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.79% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 85.03% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.47% 95.56%
CHEMBL4208 P20618 Proteasome component C5 83.02% 90.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.13% 90.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.04% 94.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.79% 94.08%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.55% 97.28%
CHEMBL3401 O75469 Pregnane X receptor 80.44% 94.73%

Plants that contains it

Top
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.
Toona ciliata

Cross-Links

Top
PubChem 42639331
LOTUS LTS0129711
wikiData Q105016276