5-[4-[6-[4-[6-[4-[2,4-Dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-2,6-dihydroxyphenoxy]-2,3,4-trihydroxyphenoxy]-2,6-dihydroxyphenoxy]-2,3,4-trihydroxyphenoxy]-2,6-dihydroxyphenoxy]-4-(3,4,5-trihydroxyphenoxy)benzene-1,2,3-triol

Details

• Internal ID: fb1cdb55-f620-4e4c-8847-6b79cdf56cf4
• Taxonomy: Phenylpropanoids and polyketides > Tannins
• IUPAC Name: 5-[4-[6-[4-[6-[4-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-2,6-dihydroxyphenoxy]-2,3,4-trihydroxyphenoxy]-2,6-dihydroxyphenoxy]-2,3,4-trihydroxyphenoxy]-2,6-dihydroxyphenoxy]-4-(3,4,5-trihydroxyphenoxy)benzene-1,2,3-triol
• InChI: InChI=1S/C54H38O31/c55-16-1-27(62)47(28(63)2-16)82-36-4-17(56)3-29(64)51(36)78-19-7-30(65)48(31(66)8-19)84-38-14-25(60)42(73)45(76)53(38)80-21-11-34(69)50(35(70)12-21)85-39-15-26(61)43(74)46(77)54(39)81-20-9-32(67)49(33(68)10-20)83-37-13-24(59)41(72)44(75)52(37)79-18-5-22(57)40(71)23(58)6-18/h1-15,55-77H
• InChI Key: IVULTGVQGICFKM-UHFFFAOYSA-N
• Popularity: 2 references in papers

Physical and Chemical Properties

• Molecular Formula: C₅₄H₃₈O₃₁
• Molecular Weight: 1182.90 g/mol
• Exact Mass: 1182.13970441 g/mol
• Topological Polar Surface Area (TPSA): 539.00 Ų
• XlogP: 6.00
• Atomic LogP (AlogP): 9.25
• H-Bond Acceptor: 31
• H-Bond Donor: 23
• Rotatable Bonds: 16

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9068	90.68%
Caco-2	-	0.8616	86.16%
Blood Brain Barrier	-	0.6250	62.50%
Human oral bioavailability	+	0.5143	51.43%
Subcellular localzation	Mitochondria	0.6716	67.16%
OATP2B1 inhibitior	+	0.5759	57.59%
OATP1B1 inhibitior	+	0.8603	86.03%
OATP1B3 inhibitior	+	0.9574	95.74%
MATE1 inhibitior	-	0.8800	88.00%
OCT2 inhibitior	-	0.9250	92.50%
BSEP inhibitior	+	0.8494	84.94%
P-glycoprotein inhibitior	+	0.7467	74.67%
P-glycoprotein substrate	-	0.9558	95.58%
CYP3A4 substrate	-	0.5910	59.10%
CYP2C9 substrate	-	0.7828	78.28%
CYP2D6 substrate	-	0.6975	69.75%
CYP3A4 inhibition	-	0.7655	76.55%
CYP2C9 inhibition	-	0.6110	61.10%
CYP2C19 inhibition	-	0.8214	82.14%
CYP2D6 inhibition	-	0.9236	92.36%
CYP1A2 inhibition	+	0.8292	82.92%
CYP2C8 inhibition	+	0.7081	70.81%
CYP inhibitory promiscuity	+	0.6451	64.51%
UGT catelyzed	+	0.6000	60.00%
Carcinogenicity (binary)	-	0.7723	77.23%
Carcinogenicity (trinary)	Non-required	0.5355	53.55%
Eye corrosion	-	0.9711	97.11%
Eye irritation	-	0.8878	88.78%
Skin irritation	+	0.5226	52.26%
Skin corrosion	-	0.7569	75.69%
Ames mutagenesis	-	0.6000	60.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.7595	75.95%
Micronuclear	+	0.6800	68.00%
Hepatotoxicity	-	0.5051	50.51%
skin sensitisation	+	0.7945	79.45%
Respiratory toxicity	+	0.5111	51.11%
Reproductive toxicity	-	0.5222	52.22%
Mitochondrial toxicity	-	0.6375	63.75%
Nephrotoxicity	+	0.5308	53.08%
Acute Oral Toxicity (c)	III	0.8994	89.94%
Estrogen receptor binding	+	0.7517	75.17%
Androgen receptor binding	+	0.7384	73.84%
Thyroid receptor binding	+	0.5972	59.72%
Glucocorticoid receptor binding	+	0.5962	59.62%
Aromatase binding	+	0.6522	65.22%
PPAR gamma	+	0.7194	71.94%
Honey bee toxicity	-	0.8325	83.25%
Biodegradation	-	0.9000	90.00%
Crustacea aquatic toxicity	+	0.6951	69.51%
Fish aquatic toxicity	+	0.9658	96.58%

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	98.10%	91.11%
CHEMBL1860	P10827	Thyroid hormone receptor alpha	96.83%	99.15%
CHEMBL3194	P02766	Transthyretin	95.06%	90.71%
CHEMBL4208	P20618	Proteasome component C5	89.74%	90.00%
CHEMBL2635	P51452	Dual specificity protein phosphatase 3	89.12%	94.00%
CHEMBL3060	Q9Y345	Glycine transporter 2	87.73%	99.17%
CHEMBL1929	P47989	Xanthine dehydrogenase	85.14%	96.12%
CHEMBL5339	Q5NUL3	G-protein coupled receptor 120	84.10%	95.78%
CHEMBL2424	Q04760	Glyoxalase I	81.10%	91.67%

Plants that contains it

There are no matching plants.

Cross-Links

• PubChem: 163194299
• LOTUS: LTS0094429
• wikiData: Q105121307