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FRAXINELLONE

fraxinellone

CAS: 28808-62-0

Molecular Formula: C14H16O3

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FRAXINELLONE - Names and Identifiers

Name fraxinellone
Synonyms fraxinellone
FRAXINELLONE
Fraxinellone
7-dimethyl-3a
(3R,3aR)-3-(3-Furyl)-3a
4,5,6-tetrahydro-2-benzofuran-1(3H)-one
tetrahydro-3a,7-dimethyl-,(3R,3aR)- (9CI)
1(3H)-Isobenzofuranone,3-(3-furanyl)-3a,4,5,6-
3-(3-Furyl)-3a,4,5,6-tetrahydro-3a,7-dimethylphthalide
(3R)-3β-(3-Furyl)-3a,4,5,6-tetrahydro-3aβ,7-dimethylisobenzofuran-1(3H)-one
(3R)-3β-(3-Furanyl)-3aβ,7-dimethyl-1,3,3a,4,5,6-hexahydroisobenzofuran-1-one
(3R,3aR)-3-(3-Furyl)-3a,7-diMethyl-3a,4,5,6-tetrahydro-2-benzofuran-1(3H)-one
1(3H)-Isobenzofuranone,3-(3-furanyl)-3a,4,5,6-tetrahydro-3a,7-diMethyl-,(3R-cis)
(3R,3aR)-3-(furan-3-yl)-3a,7-dimethyl-3a,4,5,6-tetrahydro-2-benzofuran-1(3H)-one
1(3H)-isobenzofuranone, 3-(3-furanyl)-3a,4,5,6-tetrahydro-3a,7-dimethyl-, (3R,3aR)-
CAS 28808-62-0
InChI InChI=1/C14H16O3/c1-9-4-3-6-14(2)11(9)13(15)17-12(14)10-5-7-16-8-10/h5,7-8,12H,3-4,6H2,1-2H3/t12-,14+/m0/s1

FRAXINELLONE - Physico-chemical Properties

Molecular FormulaC14H16O3
Molar Mass232.27
Density1.1649 (rough estimate)
Melting Point114.0 to 118.0 °C
Boling Point314.44°C (rough estimate)
Specific Rotation(α)(EtOH)-44
Flash Point179.3°C
Solubility Easily soluble in chloroform and ethyl acetate.
Vapor Presure9.29E-06mmHg at 25°C
AppearanceColorless needle crystal
Storage ConditionKeep in dark place,Sealed in dry,Store in freezer, under -20°C
Refractive Index1.5557 (estimate)
MDLMFCD11101451
Physical and Chemical Properties化学性质 白色结晶粉末,易溶于氯仿、乙酸乙酯,来源于白鲜皮,白柳(Salix alba L.)的皮。
UseUses tryptanthrin is an insecticide that inhibits larval growth and is used for the treatment and protection of crops and agricultural products. Also, it is a natural compound that can be used to treat tumors.
In vitro study Fraxinellone (0-100 μM;12 hours) decreases the percent of PD-L1 positive cells from 20.4% to 11.4% in A549 cells. Cell Viability Assay Cell Line: A549 cells Concentration: 0 μM, 10 μM, 30 μM, 100 μM Incubation Time: 12 hours Result: Inhibited the percent of PD-L1 positive cells.
In vivo study Fraxinellone (oral gavage; 30 and 100 mg/kg; every three days; 30 days) significantly suppresses tumor growth, reduces HIF-1α, pTyr705 STAT3, PD-L1 and VEGF staining compared with the control group in female athymic BALB/c nude mice. Animal Model: BALB/c nude mice Dosage: 30 and 100 mg/kg Administration: Oral gavage; 30 and 100 mg/kg; every three days; 30 days Result: Significantly suppressed tumor growth.

FRAXINELLONE - Risk and Safety

Safety Description24/25 - Avoid contact with skin and eyes.
UN IDsUN 2811 6.1/PG III
RTECSTI3767000
HS Code29321900
Hazard Class6.1
Packing GroupIII

FRAXINELLONE - Reference

Reference
Show more
1. Zuorui, Wang Xibin. Effect of fluorenone on LPS-mediated proliferation and migration of MH7A cells [J]. Chinese traditional medicines, 2019, 041(008):1806-1810.
2. [IF = 4.411] Zhixin Wang et al."Rapid Characterization of Chemical Components in Edible room sparsis crispa by UPLC-Orbitrap MS Analysis and Potential Effects on Allergic retinopathy." Molecules. 2019 Jan;24(16):3014

FRAXINELLONE - Uses and synthesis methods

biological activity

Fraxinellone were isolated from the root bark of the Brassicaceae plant Dictamnus dasycarpus. Fraxinellone are PD-L1 inhibitors that inhibit HIF-1α protein synthesis without affecting HIF-1α protein degradation. Fraxinellone has the potential for cancer immunity through targeted PD-L1.

in vitro study

Fraxinellone (0-100 μM;12 hours) decreases the percent of PD-L1 positive cells from 20.4% to 11.4% in A549 cells.

Cell Viability Assay

Cell Line: A549 cells

Concentration: 0 μM, 10 μM, 30 μM, 100 μM

Incubation Time: 12 hours

Result: Inhibited the percent of PD-L1 positive cells.

in vivo studies

Fraxinellone (oral gavage; 30 and 100 mg/kg; every three days; 30 days) significantly suppresses tumor growth, reduces HIF-1α, pTyr705 STAT3, PD-L1 and VEGF staining compared with the control group in female athymic BALB/c nude mice.

Animal Model: BALB/c nude mice

Dosage: 30 and 100 mg/kg

Administration: Oral gavage; 30 and 100 mg/kg; every three days; 30 days

Result: Significantly suppressed tumor growth.

use

1. Fraxinone has the functions of protecting liver and killing insects.

2, used for content determination/identification/pharmacological experiment, etc.

Pharmacological effects: anti-fertility effect, anti-platelet aggregation effect, significant vascular relaxation effect. Selective calcium channel blocking effect, and in a voltage-dependent relationship.

Last Update:2024-04-09 20:52:54

FRAXINELLONE - Reference Information

Use fluorenone is an insecticide that inhibits larval growth and is used for the treatment and protection of crops and agricultural products. Also, it is a natural compound that can be used to treat tumors.
fluorenone has hepatoprotective and insecticidal effects.
for content determination/identification/pharmacological experiments. Pharmacological Efficacy: anti-fertility, anti-platelet aggregation, significant vascular relaxation. Selective calcium channel blockade in a voltage-dependent manner.
biological activity Fraxinellone was isolated from the root bark of the brassica plant Dictamnus dasycarpus. Fraxinellone is a PD-L1 inhibitor that inhibits HIF-1α protein synthesis without affecting HIF-1α protein degradation. By targeting PD-L1, Fraxinellone has the potential for cancer immunity.
in vitro study Fraxinellone (0-100μm; 12 hours) reduce the percentage of PD-L1 positive cells from 20.4% to 11.4% in A549 cells. Cell viabilityassay Cell Line: A549 cells Concentration: 0 μm, 10 μm, 30 μm, 100 μm Incubation Time: 12 hours Result: Inhibited the percentage of PD-L1 positive cells.
Cell Line: A549 cells
Concentration: 0 μM, 10 μM, 30 μM, 100 μM
Incubation Time: 12 hours
Result: Inhibited the percent of PD-L1 positive cells.
Significantly suppressed tumor growth.
in vivo studies Fraxinellone (oral gaugan; 30 and 100   mg/kg; every three days; 30 days) significant indications tumor growth, redutions HIF-1α, pTyr705 STAT3, PD-L1 and VEGF staining compared with the control group in female nude BALB/c nude mice. Animal Model: BALB/c nude mice Dosage: 30 and 100   mg/kg Administration: Oral gavage; 30 and 100 mg/kg; every three days; 30 days Result: Significantly suppressed tumor growth.
Animal Model: BALB/c nude mice
Dosage: 30 and 100 mg/kg
Administration: Oral gavage; 30 and 100 mg/kg; every three days; 30 days
Chemical properties white crystalline powder, soluble in chloroform, ethyl acetate, derived from white fresh bark, Salix alba L. Of the skin.
Last Update:2024-04-09 21:54:55
FRAXINELLONE
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CAS: 28808-62-0
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
WhatsApp: +86-18821248368
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CAS: 28808-62-0
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
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SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
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Email: product@acmec-e.com
Mobile: +86-18621343501
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CAS: 28808-62-0
Tel: 609-228-6898
Email: sales@medchemexpress.com
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SKYRUN INDUSTRIAL CO.,LTD
Spot supply
Product Name: Fraxinellone Visit Supplier Webpage Request for quotation
CAS: 28808-62-0
Tel: +86 0571-86722205
Email: sales@chinaskyrun.com
Mobile: +8618958170122
QQ: 2531159185 Click to send a QQ messageSend QQ message
Wechat: chinaskyrun
Shanghai Yuanye Bio-Technology Co., Ltd.
Spot supply
Product Name: Fraxinellone Visit Supplier Webpage Request for quotation
CAS: 28808-62-0
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
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