[3,5-Diacetyloxy-4-[3,5-diacetyloxy-4-[3,5-diacetyloxy-4-[3,5-diacetyloxy-4-[3,5-diacetyloxy-4-(3,4,5-triacetyloxyphenoxy)phenoxy]phenoxy]phenoxy]phenoxy]phenyl] acetate

Details

• Internal ID: 4ab855a7-0c46-405a-b1bd-069123e6fa9f
• Taxonomy: Phenylpropanoids and polyketides > Tannins
• IUPAC Name: [3,5-diacetyloxy-4-[3,5-diacetyloxy-4-[3,5-diacetyloxy-4-[3,5-diacetyloxy-4-[3,5-diacetyloxy-4-(3,4,5-triacetyloxyphenoxy)phenoxy]phenoxy]phenoxy]phenoxy]phenyl] acetate
• InChI: InChI=1S/C64H54O33/c1-27(65)79-41-15-49(82-30(4)68)60(50(16-41)83-31(5)69)94-43-19-53(86-34(8)72)62(54(20-43)87-35(9)73)96-45-23-57(90-38(12)76)64(58(24-45)91-39(13)77)97-46-25-55(88-36(10)74)63(56(26-46)89-37(11)75)95-44-21-51(84-32(6)70)61(52(22-44)85-33(7)71)93-42-17-47(80-28(2)66)59(92-40(14)78)48(18-42)81-29(3)67/h15-26H,1-14H3
• InChI Key: SLFCHAJCWGLTLB-UHFFFAOYSA-N
• Popularity: 2 references in papers

Physical and Chemical Properties

• Molecular Formula: C₆₄H₅₄O₃₃
• Molecular Weight: 1351.10 g/mol
• Exact Mass: 1350.2547342 g/mol
• Topological Polar Surface Area (TPSA): 414.00 Ų
• XlogP: 6.10
• Atomic LogP (AlogP): 9.60
• H-Bond Acceptor: 33
• H-Bond Donor: 0
• Rotatable Bonds: 24

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9897	98.97%
Caco-2	-	0.8477	84.77%
Blood Brain Barrier	-	0.5500	55.00%
Human oral bioavailability	+	0.5429	54.29%
Subcellular localzation	Mitochondria	0.8827	88.27%
OATP2B1 inhibitior	+	0.5706	57.06%
OATP1B1 inhibitior	+	0.9440	94.40%
OATP1B3 inhibitior	+	0.9094	90.94%
MATE1 inhibitior	-	0.9200	92.00%
OCT2 inhibitior	-	0.9500	95.00%
BSEP inhibitior	+	0.9661	96.61%
P-glycoprotein inhibitior	+	0.7780	77.80%
P-glycoprotein substrate	-	0.9703	97.03%
CYP3A4 substrate	-	0.6400	64.00%
CYP2C9 substrate	-	0.8046	80.46%
CYP2D6 substrate	-	0.8564	85.64%
CYP3A4 inhibition	-	0.8264	82.64%
CYP2C9 inhibition	-	0.8662	86.62%
CYP2C19 inhibition	-	0.7550	75.50%
CYP2D6 inhibition	-	0.9590	95.90%
CYP1A2 inhibition	+	0.8814	88.14%
CYP2C8 inhibition	-	0.7969	79.69%
CYP inhibitory promiscuity	-	0.5757	57.57%
UGT catelyzed	-	0.0000	0.00%
Carcinogenicity (binary)	-	0.7297	72.97%
Carcinogenicity (trinary)	Non-required	0.5971	59.71%
Eye corrosion	-	0.9699	96.99%
Eye irritation	-	0.8905	89.05%
Skin irritation	-	0.8724	87.24%
Skin corrosion	-	0.9814	98.14%
Ames mutagenesis	-	0.6800	68.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.7540	75.40%
Micronuclear	+	0.5807	58.07%
Hepatotoxicity	+	0.6785	67.85%
skin sensitisation	-	0.8985	89.85%
Respiratory toxicity	-	0.8667	86.67%
Reproductive toxicity	-	0.5386	53.86%
Mitochondrial toxicity	-	0.7250	72.50%
Nephrotoxicity	+	0.7163	71.63%
Acute Oral Toxicity (c)	III	0.7509	75.09%
Estrogen receptor binding	+	0.7794	77.94%
Androgen receptor binding	+	0.5714	57.14%
Thyroid receptor binding	+	0.6288	62.88%
Glucocorticoid receptor binding	+	0.7253	72.53%
Aromatase binding	+	0.6614	66.14%
PPAR gamma	+	0.7210	72.10%
Honey bee toxicity	-	0.6885	68.85%
Biodegradation	-	0.8750	87.50%
Crustacea aquatic toxicity	-	0.5949	59.49%
Fish aquatic toxicity	+	0.9955	99.55%

Targets

Proven Targets:

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	91.06%	91.11%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	89.24%	96.09%
CHEMBL3060	Q9Y345	Glycine transporter 2	85.86%	99.17%
CHEMBL4208	P20618	Proteasome component C5	84.95%	90.00%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	84.59%	95.56%
CHEMBL1966	Q02127	Dihydroorotate dehydrogenase	84.17%	96.09%
CHEMBL1293249	Q13887	Kruppel-like factor 5	82.27%	86.33%
CHEMBL2581	P07339	Cathepsin D	81.68%	98.95%
CHEMBL2635	P51452	Dual specificity protein phosphatase 3	80.94%	94.00%

Plants that contains it

There are no matching plants.

Cross-Links

• PubChem: 16182804
• LOTUS: LTS0156189
• wikiData: Q105255263