7,16-Diethyl-4-hydroxy-5,9,13,15-tetramethyl-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-1-oxacyclohexadeca-11,13-diene-2,10-dione

Details

Top
Internal ID d80cc95f-dc22-4ca4-8a00-1ca624859c2d
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 7,16-diethyl-4-hydroxy-5,9,13,15-tetramethyl-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-1-oxacyclohexadeca-11,13-diene-2,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H48O9/c1-8-20-13-16(4)21(30)11-10-15(3)12-17(5)23(9-2)37-24(32)14-22(31)18(6)28(20)38-29-27(35)26(34)25(33)19(7)36-29/h10-12,16-20,22-23,25-29,31,33-35H,8-9,13-14H2,1-7H3
InChI Key HVTQLPWTUIEUBT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C29H48O9
Molecular Weight 540.70 g/mol
Exact Mass 540.32983310 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 7,16-Diethyl-4-hydroxy-5,9,13,15-tetramethyl-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-1-oxacyclohexadeca-11,13-diene-2,10-dione

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7726 77.26%
Caco-2 - 0.7809 78.09%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.6693 66.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8545 85.45%
OATP1B3 inhibitior + 0.9092 90.92%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5841 58.41%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate + 0.5085 50.85%
CYP3A4 substrate + 0.6468 64.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8989 89.89%
CYP3A4 inhibition - 0.7227 72.27%
CYP2C9 inhibition - 0.9011 90.11%
CYP2C19 inhibition - 0.7824 78.24%
CYP2D6 inhibition - 0.9241 92.41%
CYP1A2 inhibition - 0.9364 93.64%
CYP2C8 inhibition - 0.5962 59.62%
CYP inhibitory promiscuity - 0.9637 96.37%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6743 67.43%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.9465 94.65%
Skin irritation - 0.6509 65.09%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis - 0.5754 57.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3682 36.82%
Micronuclear - 0.5841 58.41%
Hepatotoxicity - 0.5019 50.19%
skin sensitisation - 0.7965 79.65%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7516 75.16%
Acute Oral Toxicity (c) III 0.6173 61.73%
Estrogen receptor binding + 0.7989 79.89%
Androgen receptor binding - 0.4844 48.44%
Thyroid receptor binding - 0.5406 54.06%
Glucocorticoid receptor binding + 0.6409 64.09%
Aromatase binding + 0.5774 57.74%
PPAR gamma + 0.5523 55.23%
Honey bee toxicity - 0.7317 73.17%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9261 92.61%

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
CHEMBL3714130 P46095 G-protein coupled receptor 6 96.14% 97.36%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.14% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.96% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.03% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.68% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.57% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.32% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.70% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.33% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.83% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.89% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.25% 100.00%

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.
There are no matching plants.

Cross-Links

Top
PubChem 162954471
LOTUS LTS0151224
wikiData Q104168441