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Homopterocarpin

CAS# 606-91-7

Homopterocarpin

2D Structure

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Quality Control of Homopterocarpin

3D structure

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Homopterocarpin

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Chemical Properties of Homopterocarpin

Cas No. 606-91-7 SDF Download SDF
PubChem ID 101795 Appearance Oil
Formula C17H16O4 M.Wt 284.31
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (6aR,11aR)-3,9-dimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene
SMILES COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC
Standard InChIKey VPGIGLKLCFOWDN-YOEHRIQHSA-N
Standard InChI InChI=1S/C17H16O4/c1-18-10-4-6-13-15(7-10)20-9-14-12-5-3-11(19-2)8-16(12)21-17(13)14/h3-8,14,17H,9H2,1-2H3/t14-,17-/m0/s1
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Homopterocarpin

The roots of Sophora tonkinensis

Biological Activity of Homopterocarpin

Description1. Homopterocarpin and Pterocarpus extract offer gastroprotection against indomethacin- induced ulcer by antioxidative mechanism and the modulation of gastric homeostasis, homopterocarpin may be responsible for, or contribute to the antiulcerogenic property of P. erinaceus. 2. Homopterocarpin can inhibit (lower concentration) or kill (higher concntration) human^s liver cancer cells under the cultured condition, they have anticancer activity. 3. Homopterocarpin can contribute to the hepatoprotective and antioxidant potentials of P. erinaceus extract in acetaminophen-provoked hepatotoxicity. 4. (-)-Homopterocarpin has active insect antifeedant against both S. litura and R. speratus. 5. (+)-Homopterocarpin has antimitotic effect.
TargetsAntifection

Homopterocarpin Dilution Calculator

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Homopterocarpin Molarity Calculator

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Preparing Stock Solutions of Homopterocarpin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.5173 mL 17.5864 mL 35.1729 mL 70.3457 mL 87.9322 mL
5 mM 0.7035 mL 3.5173 mL 7.0346 mL 14.0691 mL 17.5864 mL
10 mM 0.3517 mL 1.7586 mL 3.5173 mL 7.0346 mL 8.7932 mL
50 mM 0.0703 mL 0.3517 mL 0.7035 mL 1.4069 mL 1.7586 mL
100 mM 0.0352 mL 0.1759 mL 0.3517 mL 0.7035 mL 0.8793 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Homopterocarpin

Homopterocarpin contributes to the restoration of gastric homeostasis by Pterocarpus erinaceus following indomethacin intoxication in rats.[Pubmed:23375033]

Asian Pac J Trop Med. 2013 Mar;6(3):200-4.

OBJECTIVE: To investigate the restorative effect of Pterocarpus erinaceus (P. erinaceus) and Homopterocarpin, an isoflavonoid isolated from it, on indomethacin-induced disruption in gastric homeostasis in rats. METHODS: Adult rats were divided into five groups and fasted for 48 h before treatment. Group 1 received olive oil (vehicle), group 2 received 25 mg/kg indomethacin while groups 3-5 received cimetidine (100 mg/kg), Homopterocarpin (25 mg/kg) and P. erinaceus ethanolic stem bark extract (100 mg/kg) respectively. After 1 h, all the groups except group 2 were administered 25 mg/kg of indomethacin. One hour later, the rats were sacrificed and the ulcer index and other gastroprotective indices were evaluated. RESULTS: Indomethacin caused significant injury to the stomach of the rats as reflected in the ulcer indices (9.0+/-1.4) as compared with that of control (2.0+/-0.0). Equally, there were significant increases in gastric acid concentration and malondialdehyde level in the stomachs of the ulcerated animals compared with the control. However mucus content, reduced gluthatione level and gastric pH were significantly reduced in the ulcerated animals compared with the control. Pretreatment with either Pterocarpus bark extract or Homopterocarpin reversed the effects of indomethacin on the evaluated parameters. CONCLUSIONS: These results indicate that both Homopterocarpin and Pterocarpus extract offered gastroprotection against indomethacin-induced ulcer by antioxidative mechanism and the modulation of gastric homeostasis. The results also suggest that Homopterocarpin might be responsible for, or contribute to the antiulcerogenic property of P. erinaceus.

Effect of homopterocarpin, an isoflavonoid from Pterocarpus erinaceus, on indices of liver injury and oxidative stress in acetaminophen-provoked hepatotoxicity.[Pubmed:25811665]

J Basic Clin Physiol Pharmacol. 2015 Nov;26(6):555-62.

BACKGROUND: Novel hepatoprotectives are needed to address the increasing cases of liver problems worldwide. Pterocarpus erinaceus Poir (Fabaceae) ethanol stem bark extract (PE) and its constituent flavonoid, Homopterocarpin (HP), were investigated for their protective property in acetaminophen-induced oxidative stress and liver damage. METHODS: Adult male albino rats were divided into nine groups. Seven groups were pretreated with PE (50-, 100-, and 150 mg/kg), HP (25-, 50-, and 75 mg/kg) or silymarin (25 mg/kg), respectively, once daily for 5 consecutive days and then administered acetaminophen (2 g/kg) on the 5th day. The control and acetaminophen-intoxicated groups received normal saline throughout the experimental period, with the latter group additionally receiving 2 g/kg acetaminophen on the 5th day. Administrations were performed po. RESULTS: In the acetaminophen-intoxicated group, there were significant increases (p<0.05) in serum activities of alanine aminotransferase (31.72+/-3.3 vs. 22.1+/-1.2 U/I), aspartate aminotransferase (185.1+/-10.1 vs. 103.83+/-13.3 U/I), bilirubin level and hepatic malondialdehyde (2.32+/-0.3 vs. 1.42+/-0.1 units/mg protein), accompanied with significant decreases (p<0.05) in hepatic reduced glutathione level (0.10+/-0.01 vs. 0.23+/-0.03 units/mg protein) and glutathione peroxidase activity (2.51+/-0.2 vs. 3.25+/-0.2 mumol H2O2 consumed/min/mg protein) compared with the control. CONCLUSIONS: PE and HP ameliorated most of the observed biochemical alterations with HP appearing to show more potency. The results suggest that the flavonoid, Homopterocarpin contributes to the hepatoprotective and antioxidant potentials of P. erinaceus extract.

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