Gnetin H

Details

• Internal ID: f72a5014-28bd-4f52-ba4f-a2d5a44aa5a7
• Taxonomy: Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
• IUPAC Name: 5-[(2S,3S,5S,6S)-3-(3,5-dihydroxyphenyl)-2,6-bis(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3,5,6-tetrahydrofuro[3,2-f][1]benzofuran-5-yl]benzene-1,3-diol
• SMILES (Canonical): C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC4=C2C(C(O4)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O
• SMILES (Isomeric): C1=CC(=CC=C1/C=C/C2=C3[C@@H]([C@H](OC3=CC4=C2[C@@H]([C@H](O4)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O
• InChI: InChI=1S/C42H32O9/c43-27-8-1-22(2-9-27)3-14-34-39-35(50-41(23-4-10-28(44)11-5-23)37(39)25-15-30(46)19-31(47)16-25)21-36-40(34)38(26-17-32(48)20-33(49)18-26)42(51-36)24-6-12-29(45)13-7-24/h1-21,37-38,41-49H/b14-3+/t37-,38-,41+,42+/m0/s1
• InChI Key: PHIHHTIYURVLDB-JPZOQBBBSA-N
• Popularity: 7 references in papers

Physical and Chemical Properties

• Molecular Formula: C₄₂H₃₂O₉
• Molecular Weight: 680.70 g/mol
• Exact Mass: 680.20463259 g/mol
• Topological Polar Surface Area (TPSA): 160.00 Ų
• XlogP: 7.70
• Atomic LogP (AlogP): 8.33
• H-Bond Acceptor: 9
• H-Bond Donor: 7
• Rotatable Bonds: 6

Synonyms

• trans-Gnetin H
• (+)-trans-Gnetin H
• 105132-92-1
• UNII-2RXU4J2Z19
• 2RXU4J2Z19
• 1,3-Benzenediol, 5,5'-((2S,3S,5S,6S)-2,3,5,6-tetrahydro-2,6-bis(4-hydroxyphenyl)-4-((1E)-2-(4-hydroxyphenyl)ethenyl)benzo(1,2-b:5,4-b')difuran-3,5-diyl)bis-
• 1,3-Benzenediol, 5,5'-[(2S,3S,5S,6S)-2,3,5,6-tetrahydro-2,6-bis(4-hydroxyphenyl)-4-[(1E)-2-(4-hydroxyphenyl)ethenyl]benzo[1,2-b:5,4-b']difuran-3,5-diyl]bis-
• SCHEMBL14255845
• DTXSID301319156
• AKOS040736399
• Q27255515
• 5-[(2S,3S,5S,6S)-3-(3,5-dihydroxyphenyl)-2,6-bis(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3,5,6-tetrahydrofuro[3,2-f][1]benzofuran-5-yl]benzene-1,3-diol

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9881	98.81%
Caco-2	-	0.8300	83.00%
Blood Brain Barrier	-	0.7000	70.00%
Human oral bioavailability	-	0.7000	70.00%
Subcellular localzation	Mitochondria	0.5535	55.35%
OATP2B1 inhibitior	+	0.5695	56.95%
OATP1B1 inhibitior	+	0.7760	77.60%
OATP1B3 inhibitior	+	0.8015	80.15%
MATE1 inhibitior	-	0.9800	98.00%
OCT2 inhibitior	-	0.9500	95.00%
BSEP inhibitior	+	0.8169	81.69%
P-glycoprotein inhibitior	+	0.7556	75.56%
P-glycoprotein substrate	-	0.9203	92.03%
CYP3A4 substrate	-	0.5286	52.86%
CYP2C9 substrate	+	0.6202	62.02%
CYP2D6 substrate	+	0.3681	36.81%
CYP3A4 inhibition	+	0.6476	64.76%
CYP2C9 inhibition	+	0.9283	92.83%
CYP2C19 inhibition	+	0.8370	83.70%
CYP2D6 inhibition	-	0.8256	82.56%
CYP1A2 inhibition	+	0.8993	89.93%
CYP2C8 inhibition	+	0.7283	72.83%
CYP inhibitory promiscuity	+	0.9650	96.50%
UGT catelyzed	+	0.6000	60.00%
Carcinogenicity (binary)	-	0.9100	91.00%
Carcinogenicity (trinary)	Danger	0.4413	44.13%
Eye corrosion	-	0.9892	98.92%
Eye irritation	-	0.6688	66.88%
Skin irritation	+	0.5125	51.25%
Skin corrosion	-	0.9324	93.24%
Ames mutagenesis	+	0.5400	54.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.8537	85.37%
Micronuclear	+	0.8400	84.00%
Hepatotoxicity	-	0.5769	57.69%
skin sensitisation	-	0.6900	69.00%
Respiratory toxicity	-	0.6333	63.33%
Reproductive toxicity	-	0.5111	51.11%
Mitochondrial toxicity	-	0.5000	50.00%
Nephrotoxicity	+	0.5000	50.00%
Acute Oral Toxicity (c)	II	0.4136	41.36%
Estrogen receptor binding	+	0.7482	74.82%
Androgen receptor binding	+	0.8147	81.47%
Thyroid receptor binding	+	0.7153	71.53%
Glucocorticoid receptor binding	+	0.6695	66.95%
Aromatase binding	-	0.5333	53.33%
PPAR gamma	+	0.7825	78.25%
Honey bee toxicity	-	0.8437	84.37%
Biodegradation	-	0.9250	92.50%
Crustacea aquatic toxicity	+	0.6000	60.00%
Fish aquatic toxicity	+	0.9801	98.01%

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	97.10%	91.11%
CHEMBL4040	P28482	MAP kinase ERK2	93.24%	83.82%
CHEMBL3194	P02766	Transthyretin	92.14%	90.71%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	91.51%	95.56%
CHEMBL1806	P11388	DNA topoisomerase II alpha	89.24%	89.00%
CHEMBL1951	P21397	Monoamine oxidase A	89.12%	91.49%
CHEMBL3401	O75469	Pregnane X receptor	85.64%	94.73%
CHEMBL242	Q92731	Estrogen receptor beta	85.01%	98.35%
CHEMBL3137262	O60341	LSD1/CoREST complex	84.30%	97.09%
CHEMBL2563	Q9UQL6	Histone deacetylase 5	83.65%	89.67%
CHEMBL1075094	Q16236	Nuclear factor erythroid 2-related factor 2	83.30%	96.00%
CHEMBL3192	Q9BY41	Histone deacetylase 8	82.51%	93.99%
CHEMBL1293249	Q13887	Kruppel-like factor 5	80.79%	86.33%

Plants that contains it

• Paeonia lactiflora
• Vitis vinifera

Cross-Links

• PubChem: 9852931
• LOTUS: LTS0015265
• wikiData: Q27255515