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Product
Ginkgo Biloba Leaf Extract 1.Ginkgo biloba leaf extract is an effective anti-oxidant.2.Ginkgo biloba leaf extract can be used for anti-cancer and preventing cancer.3.Ginkgo biloba leaf extract can promot cerebral blood circulation and cellular metabolism.4.Ginkgo biloba leaf extract has the function of lowering blood pressure and high blood fat.5.Ginkgo biloba leaf extract is tonifying kidney and nourishing brain, whitening and anti-wrinkle.6.Ginkgo biloba leaf extract is effective on dilating blood vessels, promoting blood circulation and enhancing immunity. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ginkgo Biloba Leaf Extract. Product Category: Material of cosmetics. Appearance: Yellow brown fine powder. CAS No. 90045-36-6. Product ID: ACM90045366. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
Ginkgo Biloba Leaf Powder & P.E. 4:1 Ginkgo Biloba Leaf Powder & P.E. 4:1. Pharma Resources International LLC
CA, FL & NJ
Ginkgo Biloba Terpene Lactones Mix 100 ?g/mL each component in acetonitrile, ampule of 1.0 mL, certified reference material. Group: Herbal medicinal products standards. Alfa Chemistry Analytical Products
Ginkgolic Acid Ginkgolic Acid. CAS No: 22910-60-7 Sarchem Laboratories
Sarchem Laboratories New Jersey NJ
Ginkgolic Acid Ginkgolic Acid is a natural compound that inhibits SUMOylation with an IC 50 of 3.0 μM in in vitro assay. Uses: Scientific research. Group: Natural products. Alternative Names: Ginkgolic acid (15:1); Ginkgolic acid I; Romanicardic acid. CAS No. 22910-60-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0077. MedChemExpress MCE
Ginkgolic acid 15:1 Ginkgolic acid 15:1. Group: Biochemicals. CAS No. 22910-60-7. Pack Sizes: 5mg. US Biological Life Sciences. USBiological 9
Worldwide
Ginkgolic Acid (15:1) - CAS 22910-60-7 A cell-permeable anacardic acid analog that inhibits protein SUMO. Group: Fluorescence/luminescence spectroscopy. Alfa Chemistry Analytical Products
Ginkgolic acid 17:1 Ginkgolic acid 17:1. Group: Biochemicals. CAS No. 111047-30-4. Pack Sizes: 5mg. US Biological Life Sciences. USBiological 9
Worldwide
Ginkgolic acid (C13:0) Ginkgolic acid (C13:0). Group: Biochemicals. Grades: Highly Purified. CAS No. 20261-38-5. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. Molecular Formula: C20H32O3. US Biological Life Sciences. USBiological 7
Worldwide
Ginkgolic Acid (C13:0) Ginkgolic Acid (C13:0) is a natural anticariogenic agent in that it exhibits antimicrobial activity against S. Uses: Scientific research. Group: Natural products. Alternative Names: Ginkgolic acid (13:0); Ginkgoneolic Acid; 6-Tridecylsalicylic acid. CAS No. 20261-38-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N0078. MedChemExpress MCE
Ginkgolic Acid C13-0 Ginkgolic Acid C13-0. Group: Biochemicals. Alternative Names: Ginkgolic Acid C13:0. Grades: Plant Grade. CAS No. 20261-38-5. Pack Sizes: 10mg. Molecular Formula: C20H32O3, Molecular Weight: 320.466. US Biological Life Sciences. USBiological 9
Worldwide
ginkgolic acid (C15:1) ginkgolic acid (C15:1). Group: Biochemicals. Grades: Highly Purified. CAS No. 22910-60-7. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. Molecular Formula: C22H34O3. US Biological Life Sciences. USBiological 7
Worldwide
Ginkgolic Acid (C15:1) Ginkgolic Acid is a natural compound with suspected cytotoxic, allergenic, mutagenic and carcinogenic properties. Synonyms: Ginkgoic acid; AK-46666; AK46666; AK 46666; HY-N0077; HYN0077; HY N0077; Ginkgolic acid (15:1); Ginkgolic acid I; Romanicardic acid. Grades: >98%. CAS No. 22910-60-7. Molecular formula: C22H34O3. Mole weight: 346.5. BOC Sciences 11
Ginkgolic Acid C15-1 Ginkgolic Acid C15-1. Group: Biochemicals. Alternative Names: Ginkgolic Acid C15:1; Ginkgoic acid; Ginkgolic acid; Romanicardic acid; (15:1)-Anacardic acid; Ana B. Grades: Plant Grade. CAS No. 22910-60-7. Pack Sizes: 20mg. Molecular Formula: C22H34O3, Molecular Weight: 346.504. US Biological Life Sciences. USBiological 9
Worldwide
Ginkgolic acid (C17:1) Ginkgolic acid (C17:1). Group: Biochemicals. Grades: Highly Purified. CAS No. 111047-30-4. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C24H38O3. US Biological Life Sciences. USBiological 7
Worldwide
Ginkgolic acid C17:1 Ginkgolic acid C17:1 is a fatty acid synthase ( FAS ) inhibitor with an IC 50 of 10.5 μM. Ginkgolic acid C17:1 shows anti-tumor activity by inhibiting the phosphorylation of STAT3 and inducing apoptosis. Ginkgolic acid C17:1 can block the interaction between S-RBD and ACE2 , and has anti- SARS-CoV-2-S pseudovirus activity. Ginkgolic acid C17:1 inhibits the biofilm formation of enterohemorrhagic Escherichia coli and Staphylococcus aureus [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 111047-30-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N2116. MedChemExpress MCE
Ginkgolic Acid C17-1 Ginkgolic Acid C17-1. Group: Biochemicals. Alternative Names: Ginkgolic Acid C17:1. Grades: Plant Grade. CAS No. 111047-30-4. Pack Sizes: 10mg. Molecular Formula: C24H38O3, Molecular Weight: 374.557. US Biological Life Sciences. USBiological 9
Worldwide
Ginkgolic Acids United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Ginkgolic Acids. Alfa Chemistry Analytical Products 4
Ginkgolide A Family of bioactive terpenes treating cardiovascular and cerebrovascular diseases. Specific platelet activating factor (PAF) antagonists. Group: Biochemicals. Alternative Names: (1R, 3S, 3aS, 4R, 6aR, 7aR, 7bR, 8S, 10aS, 11aS) -3- (1, 1-Dimethylethyl) hexahydro-4, 7b-dihydroxy-8-methyl-9H-1, 7a- (epoxymethano) -1H, 6aH-cyclopenta[c]furo[2, 3-b]furo[3', 2': 3, 4]cyclopenta[1, 2-d]furan-5, 9, 12 (4H) -trione; BN 52020. Grades: Highly Purified. CAS No. 15291-75-5. Pack Sizes: 100mg. US Biological Life Sciences. USBiological 2
Worldwide
Ginkgolide A Ginkgolide A (BN-52020) is an extract from in Ginkgo biloba and a g-aminobutyric acid (GABA) antagonist. Uses: Scientific research. Group: Natural products. Alternative Names: BN-52020. CAS No. 15291-75-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B0355. MedChemExpress MCE
Ginkgolide A from Ginkgo biloba leaves analytical standard, ?90% (HPLC). Group: Herbal medicinal products standards. Alfa Chemistry Analytical Products
Ginkgolide B Ginkgolide B (BN-52021), a terpene lactone, is a potent platelet activating factor antagonist. Ginkgolide B protects endothelial cells via the activation of PXR from injuries induced by xeno- and endobiotics. Ginkgolide B can pass through the brain-blood barrier. Ginkgolide B has anti-oxidant, anti-inflammatory, anti-tumor, and anti- apoptotic activity. Ginkgolide B has marked neuroprotective effects against ischemia-induced impairments [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: BN-52021. CAS No. 15291-77-7. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-N0784. MedChemExpress MCE
Ginkgolide B Family of bioactive terpenes treating cardiovascular and cerebrovascular diseases. Specific platelet activating factor (PAF) antagonists. Group: Biochemicals. Alternative Names: (1R, 3S, 3aS, 4R, 6aR, 7aR, 7bR, 8S, 10aS, 11R, 11aR) -3- (1, 1-Dimethylethyl) hexahydro-4, 7b, 11-trihydroxy-8-methyl-9H-1, 7a- (epoxymethano) -1H, 6aH-cyclopenta[c]furo[2, 3-b]furo[3', 2': 3, 4]cyclopenta[1, 2-d]furan-5, 9, 12 (4H) -trione; BN 52021. Grades: Highly Purified. CAS No. 15291-77-7. Pack Sizes: 5mg. US Biological Life Sciences. USBiological 2
Worldwide
Ginkgolide B Ginkgolide B (BN-52021), an important active terpenoid from Ginkgo biloba leaves, is reported to increase cell viability and decrease cell apoptosis.IC50 value:Target:In vitro: Ginkgolide B (0.2 or 0.4 μg/ml) was added to the culture medium in vitro led to increases in cell viability and decreases in the number of hippocampal cells undergoing AAPH-induced apoptosis. Ginkgolide B caused a dose-related protection against dysrhythmias; the antiarrhythmic effect of ginkgolide B was comparable to that of diltiazem and superior to the activity of metoprolol. Ginkgolide B can presumably prevent the re-entry mechanism involved in the development of ischemia-induced rhythm disturbances.In vivo: Oral administration of ginkgolide B (2 mg/kg/day, p.o.) caused a significant increase in cell viability and a highly significant decrease in the numbers of both spontaneously occurring and AAPH-induced apoptoses. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 7-Deoxyginkgolide C. Product Category: Inhibitors. Appearance: White powder. CAS No. 15291-77-7. Molecular formula: C20H24O10. Mole weight: 424.4. Purity: 0.98. IUPACName: (1R,3R,6R,7S,8S,10R,11R,12R,13S,16S,17R)-8-tert-butyl-6,12,17-trihydroxy-16-methyl-2,4,14,19-tetraoxahexacyclo[8.7.2.01,11.03,7.07,11.013,17]nonadecane-5,15,18-trione. Canonical SMILES: C[C@@H]1C(=O)O[C@@H]2[C@]1([C@@]34C(=O)O[C@H]5[C@]3([C@H]2O)[C@@]6([C@@H](C5)C(C)(C) Alfa Chemistry.
Ginkgolide B from Ginkgo biloba leaves ?90% (HPLC). Group: Herbal medicinal products standards. Alfa Chemistry Analytical Products
Ginkgolide C Ginkgolide C is a flavone isolated from Ginkgo biloba leaves, possessing multiple biological functions, such as decreasing platelet aggregation and ameliorating Alzheimer disease. Uses: Scientific research. Group: Natural products. Alternative Names: BN-52022. CAS No. 15291-76-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-N0785. MedChemExpress MCE
Ginkgolide C Family of bioactive terpenes treating cardiovascular and cerebrovascular diseases. Specific platelet activating factor (PAF) antagonists. Group: Biochemicals. Alternative Names: (1S, 2R, 3S, 3aS, 4R, 6aR, 7aR, 7bR, 8S, 10aS, 11R, 11aR) -3- (1, 1-Dimethylethyl) hexahydro-2, 4, 7b, 11-tetrahydroxy-8-methyl-9H-1, 7a- (epoxymethano) -1H, 6aH-cyclopenta[c]furo[2, 3-b]furo[3', 2': 3, 4]cyclopenta[1, 2-d]furan-5, 9, 12 (4H) -trione; BN 52022. Grades: Highly Purified. CAS No. 15291-76-6. Pack Sizes: 50mg. US Biological Life Sciences. USBiological 2
Worldwide
Ginkgolide J Ginkgolide J is extracted from the seed of Ginkgo biloba L. It reduces apoptotic damage in cultured chick embryonic neurons. It contributes to the antioxidant properties of G. biloba. It has the superoxide scavenging effect and neuroprotective effect. Synonyms: 7beta-hydroxyginkgolide a; BN 52024; GinkgolideA, 7-hydroxy-, (7β)-; J Ginkgoli. Grades: >98%. CAS No. 107438-79-9. Molecular formula: C20H24O10. BOC Sciences 9
Ginkgolide J analytical standard. Group: Natural compounds. Alfa Chemistry Analytical Products 2
Ginkgolide J Ginkgolide J. Group: Biochemicals. Grades: Highly Purified. CAS No. 107438-79-9. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C20H24O10. US Biological Life Sciences. USBiological 7
Worldwide
Ginkgoneolic acid Ginkgoneolic acid. Group: Biochemicals. CAS No. 20261-38-5. Pack Sizes: 5mg. US Biological Life Sciences. USBiological 9
Worldwide
Ginkgo terpene lactones United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. Alfa Chemistry Analytical Products 2
Ginkgotoxin analytical standard. Group: Herbal medicinal products standards. Alfa Chemistry Analytical Products
Ginseng extract Ginseng extract. Applications: Functional food, health care products and pharmaceuticals. Group: Others. Purity: 8%-80.0% Ginsenoside. Appearance: Off white powder. Source: Ginseng is perhaps the most widely recognized plant used in traditional medicine and now plays a major role in the herbal health care market. For more than 2, 000 years, various forms have been used medicinally. The name Panax derives from the Greek word for"all healing, " and its properties have been so touted. Ginseng roots man-shaped figure (shen-seng means "man-root") led proponents of the doctrine of signatures, an ancient European herbalists philosophy, to believe that the root could strengthen any part of the body. Through the ages, the root has been used in the treatment of asthenia, atherosclerosis, blood and bleeding disorders, and colitis, as well as to relieve the effects of aging, cancer, and senility. Ginseng extract. Cat No: EXTC-184. Creative Enzymes
Ginseng Extract Ginseng Extract. Uses: Designed for use in research and industrial production. Product Category: Material of health food. Appearance: White powder. CAS No. 90045-38-8. Molecular formula: C15H24N2O. Mole weight: 248.37. Product ID: ACM90045388. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry. 2
Ginseng Extract (Ratio) Ginseng Extract (Ratio). Group: Others. Purity: 4:1~20:1. Ginseng Extract (Ratio). Cat No: EXTW-035. Creative Enzymes
Ginseng Ginsenosides Mix 100 ?g/mL each component in methanol, ampule of 100 ?g/mL, certified reference material. Group: Herbal medicinal products standards. Alfa Chemistry Analytical Products
Ginseng, Korean extract Ginseng, Korean extract. Product ID: 10-0032. Properties: powder. CarboMer Inc
ginsenosidase type I Ginsenosidase type I is slightly activated by Mg2+ or Ca2+. The enzyme hydrolyses the 3-O-β-D-(1?2)-glucosidic bond, the 3-O-β-D-glucopyranosyl bond and the 20-O-β-D-(1?6)-glycosidic bond of protopanaxadiol-type ginsenosides. It usually leaves a single glucosyl residue attached at position 20 and one or no glucosyl residues at position 3. Starting with a ginsenoside that is glycosylated at both positions (e.g. ginsenoside Rb1, Rb2, Rb3, Rc or Rd), the most common products are ginsenoside F2 and ginsenoside C-K, with low amounts of ginsenoside Rh2. Group: Enzymes. Enzyme Commission Number: EC 3.2.1.193. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3877; ginsenosidase type I; EC 3.2.1.193. Cat No: EXWM-3877. Creative Enzymes
ginsenosidase type III Ginsenosidase type III catalyses the sequential hydrolysis of the 3-O-β-D-(1?2)-glucopyranosyl bond followed by hydrolysis of the 3-O-β-D-glucopyranosyl bond of protopanaxadiol ginsenosides. When acting for example on ginsenoside Rb1 the enzyme first generates ginsenoside XVII, and subsequently ginsenoside LXXV. Group: Enzymes. Enzyme Commission Number: EC 3.2.1.191. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3875; ginsenosidase type III; EC 3.2.1.191. Cat No: EXWM-3875. Creative Enzymes
ginsenosidase type IV Ginsenosidase type IV catalyses the sequential hydrolysis of the 6-O-β-D-(1?2)-glycosidic bond or the 6-O-α-D-(1?2)-glycosidic bond in protopanaxatriol-type ginsenosides with a disacchride attached to the C6 position, followed by the hydrolysis of the remaining 6-O-β-D-glycosidic bond (e.g. ginsenoside Re ? ginsenoside Rg1 ? ginsenoside F1). Group: Enzymes. Enzyme Commission Number: EC 3.2.1.194. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3878; ginsenosidase type IV; EC 3.2.1.194. Cat No: EXWM-3878. Creative Enzymes
Ginsenoside CK Ginsenoside compound K (C-K) is a metabolite of the protopanaxadiol-type saponins of Panax ginseng C.A. Meyer (Araliaceae), has long been used to treat against the development of cancer, inflammation, allergies, and diabetes; C-K acts as a unique HUVEC migration inhibitor by regulating MMP expression, as well as the activity of SPHK1 and its related sphingolipid metabolites. [1]Ginsenoside compound K, the intestinal metabolite of ginseng saponin, has various chemopreventive and chemotherapeutic activities, including anti-tumor activity; C-K suppresses the activation of the NF-κB pathway, may become a potential cytotoxic drug in the prevention and treatment of hepatocellular carcinoma( HCC).[2]Ginsenoside compound K shows significant anti-proliferative effects and pro-apoptotic effects in HCT-116 and SW-480 cells at concentrations of 30-50 uM, suggests that C-K could be potentially effective anti-colorectal cancer agent.[3]Ginsenoside CK has anti-cancer effect on NPC cells, C-K-induced apoptosis of HK-1 cells was mediated by the mitochondrial pathway and could significantly inhibit tumor growth in vivo.[4]. Group: Biochemicals. Alternative Names: (3 β,12 β)-3,12-Dihydroxydammar-24-en-2. Grades: Highly Purified. CAS No. 39262-14-1. Pack Sizes: 10mg, 20mg, 50mg, 100mg. Molecular Formula: C??H??O?, Molecular Weight: 622.87. US Biological Life Sciences. USBiological 9
Worldwide
Ginsenoside C-K Ginsenoside C-K, a bacterial metabolite of G-Rb1, exhibits anti-inflammatory effects by reducing iNOS and COX-2. Ginsenoside C-K exhibits an inhibition against the activity of CYP2C9 and CYP2A6 in human liver microsomes with IC50s of 32.0±3.6 ?M and 63.6±4.2 ?M, respectively. Uses: Scientific research. Group: Natural products. Alternative Names: Ginsenoside compound K; Ginsenoside K. CAS No. 39262-14-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0904. MedChemExpress MCE
Ginsenoside Compound K Ginsenoside Compound K. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Compound K; Ginsenoside K; X1141; N1890. Appearance: White powder. CAS No. 39262-14-1. Molecular formula: C36H62O8. Mole weight: 622.88. Purity: 0.98. IUPACName: (2S,3R,4S,5S,6R)-2-[(2S)-2-[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-en-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol. Canonical SMILES: CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)O)C)C)O)C)OC5C(C(C(C(O5)CO)O)O)O)C. Density: 1.19. Product ID: ACM39262141. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
Ginsenoside F1 Ginsenoside F1. Group: Biochemicals. Grades: Plant Grade. CAS No. 53963-43-2. Pack Sizes: 20mg. Molecular Formula: C36H62O9, Molecular Weight: 638.87. US Biological Life Sciences. USBiological 9
Worldwide
Ginsenoside F1 Ginsenoside F1. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3β,6α,12β-Trihydroxy-5α-dammar-24-en-20-yl β-D-glucopyranoside. Appearance: White powder. CAS No. 53963-43-2. Molecular formula: C36H62O9. Mole weight: 638.87. Purity: 0.98. IUPACName: (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(2S)-6-methyl-2-[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,6,12-trihydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]hept-5-en-2-yl]oxyoxane-3,4,5-triol. Canonical SMILES: CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(C[C@@H]([C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)O)C)O)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)C. Density: 1.23±0.1 g/ml. Product ID: ACM53963432. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry. 3
Ginsenoside F1 Ginsenoside F1, an enzymatically modified derivative of Ginsenoside Rg1, demonstrates competitive inhibition of CYP3A4 activity and weaker inhibition of CYP2D6 activity. Uses: Scientific research. Group: Natural products. Alternative Names: 20(S)-Ginsenoside F1. CAS No. 53963-43-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg. Product ID: HY-N0598. MedChemExpress MCE
Ginsenoside F2 Ginsenoside F2, a metabolite from Ginsenoside Rb1, induces apoptosis accompanied by protective autophagy in breast cancer stem cells [1]. Uses: Scientific research. Group: Natural products. CAS No. 62025-49-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-125848. MedChemExpress MCE
Ginsenoside F2 Ginsenoside F2. Group: Biochemicals. Grades: Plant Grade. CAS No. 62025-49-4. Pack Sizes: 20mg. Molecular Formula: C42H72O13, Molecular Weight: 785.01. US Biological Life Sciences. USBiological 9
Worldwide
Ginsenoside F3 Ginsenoside F3. Group: Biochemicals. Grades: Plant Grade. CAS No. 62025-50-7. Pack Sizes: 10mg. Molecular Formula: C41H70O13, Molecular Weight: 770.99. US Biological Life Sciences. USBiological 9
Worldwide
Ginsenoside F3 Ginsenoside F3 is extracted from the root of Panax ginseng C. A. Mey. It has immunoenhancing activity by regulating production and gene expression of type 1 cytokines and type 2 cytokines in murine spleen cells. Synonyms: (20S)-20-(6-O-α-L-Arabinopyranosyl-β-D-glucopyranosyloxy)-5α-dammara-24-ene-3β,6α,12β-triol; 3β,6α,12β-Trihydroxy-5α-dammar-24-en-20-yl 6-O-α-L-arabinopyranosyl-β-D-glucopyranoside. Grades: >98%. CAS No. 62025-50-7. Molecular formula: C41H70O13. BOC Sciences 9
Ginsenoside F4 Ginsenoside F4 is extracted from the root of Panax ginseng C. A. Mey. It has inhibitory effect on human lymphocytoma JK cell by inducing its apoptosis. It was found to strongly inhibit activation of p38 mitogen-activated protein kinase in signal transduction pathways. Synonyms: Ginsenoside Rg6; (20E)-Ginsenoside F4. Grades: >98%. CAS No. 181225-33-2. Molecular formula: C42H70O12. Mole weight: 767. BOC Sciences 9
Ginsenoside F4 Ginsenoside F4. Group: Biochemicals. Alternative Names: Δ20(22)-Ginsenoside Rg6. Grades: Plant Grade. CAS No. 181225-33-2. Pack Sizes: 5mg. Molecular Formula: C42H70O12, Molecular Weight: 766.998. US Biological Life Sciences. USBiological 9
Worldwide
Ginsenoside F5 Ginsenoside F5 is extracted from the root of Panax ginseng C. A. Mey. Synonyms: Chikusetsusaponin L8; (3beta,6alpha,12beta)-3,6,12-Trihydroxydammar-24-en-20-yl 6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside. Grades: >98%. CAS No. 189513-26-6. Molecular formula: C41H70O13. BOC Sciences 9
Ginsenoside Ft1 BOC Sciences 11
Ginsenoside Mb Ginsenoside Mb. Group: Biochemicals. CAS No. 88105-29-7. Pack Sizes: 5mg. US Biological Life Sciences. USBiological 9
Worldwide
Ginsenoside Ra1 Ginsenoside Ra1 is a known dammarane-type triterpene saponins isolated from the root of Panax ginseng. Panax ginseng C. A. Meyer (Araliaceae) is a well-known oriental medicinal plant that has been used as a general tonic for thousands of years. Synonyms: β-D-Glucopyranoside, (3β,?12β)?-12-hydroxy-20-[(O-β-D-xylopyranosyl-(1?4)?-O-α-L-arabinopyranosyl-(1?6)?-β-D-glucopyranosyl)?oxy]?dammar-24-en-3-yl 2-O-β-D-glucopyranosyl-; (3β,12β)-12-Hydroxy-20-[(O-β-D-xylopyranosyl-(1?4)-O-α-L-arabinopyranosyl-(1?6)-β-D-glucopyranosyl)oxy]dammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside; Dammarane, β-D-glucopyranoside deriv. Grades: > 98%. CAS No. 83459-41-0. Molecular formula: C58H98O26. Mole weight: 1211.38. BOC Sciences 9
Ginsenoside Ra2 Ginsenoside Ra2 is a known ginsenoside isolated from the root of Panax ginseng. Previous phytochemical studies on P. ginseng led to the isolation of ginsenosides (triterpenoid saponin glycosides), polyacetylenes, sesquiterpenoids, flavonoids, and polysaccharides. Synonyms: β-D-Glucopyranoside, (3β,?12β)?-12-hydroxy-20-[(O-β-D-xylopyranosyl-(1?2)?-O-α-L-arabinofuranosyl-(1?6)?-β-D-glucopyranosyl)?oxy]?dammar-24-en-3-yl 2-O-β-D-glucopyranosyl-; (3β,12β)-12-Hydroxy-20-[(O-β-D-xylopyranosyl-(1?2)-O-α-L-arabinofuranosyl-(1?6)-β-D-glucopyranosyl)oxy]dammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside; Dammarane, β-D-glucopyranoside deriv. Grades: > 98%. CAS No. 83459-42-1. Molecular formula: C58H98O26. Mole weight: 1211.38. BOC Sciences 9
Ginsenoside Ra3 Ginsenoside Ra3 is isolated from the root of Panax ginseng. Protopanaxadiol- and protopanaxatriol-type ginsenosides are the major biologically active components of P. ginseng that contribute to its diverse pharmacological effects on the central nervous system, cardiovascular system, endocrine secretion, immune-modulation, metabolism, stress, aging, and cancer. Synonyms: β-D-Glucopyranoside, (3β,?12β)?-12-hydroxy-20-[(O-β-D-xylopyranosyl-(1?3)?-O-β-D-glucopyranosyl-(1?6)?-β-D-glucopyranosyl)?oxy]?dammar-24-en-3-yl 2-O-β-D-glucopyranosyl-; (3β,12β)-12-Hydroxy-20-[(O-β-D-xylopyranosyl-(1?3)-O-β-D-glucopyranosyl-(1?6)-β-D-glucopyranosyl)oxy]dammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside; Dammarane, β-D-glucopyranoside deriv. Grades: > 98%. CAS No. 90985-77-6. Molecular formula: C59H100O27. Mole weight: 1241.41. BOC Sciences 9
Ginsenoside Rb1 Ginsenoside Rb1, a main constituent of the root of Panax ginseng, inhibits Na+, K+-ATPase activity with an IC50 of 6.3±1.0 μM. Ginsenoside also inhibits IRAK-1 activation and phosphorylation of NF-κB p65. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-O-beta-glucopyranosyl-(3beta,12beta)-20-[(6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl-beta-D-glucopyranoside. Product Category: Inhibitors. Appearance: White powder. CAS No. 41753-43-9. Molecular formula: C54H92O23. Mole weight: 1109.29. Purity: 0.98. IUPACName: (2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6S)-6-[(2S)-2-[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-en-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol. Canonical SMILES: CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)C)O)C)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O)O)O)O)O)O)C. Density: 1.097 g/ml. Product ID: ACM41753439. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
Ginsenoside Rb1 Ginsenoside Rb1. Group: Biochemicals. Alternative Names: Sanchinoside E1; Gypenoside III; Gynosaponin C. Grades: Plant Grade. CAS No. 41753-43-9. Pack Sizes: 20mg. Molecular Formula: C54H92O23, Molecular Weight: 1109.29. US Biological Life Sciences. USBiological 9
Worldwide
Ginsenoside Rb1 primary reference standard. Group: Natural compoundscarbohydrateseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alfa Chemistry Analytical Products 4
Ginsenoside Rb1 Ginsenoside Rb1, a main constituent of the root of Panax ginseng , inhibits Na + , K + -ATPase activity with an IC 50 of 6.3±1.0 μM. Ginsenoside also inhibits IRAK-1 activation and phosphorylation of NF-κB p65. Uses: Scientific research. Group: Natural products. Alternative Names: Gypenoside III. CAS No. 41753-43-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0039. MedChemExpress MCE
ginsenoside Rb1 β-glucosidase Ginsenosidases catalyse the hydrolysis of glycosyl moieties attached to the C-3, C-6 or C-20 position of ginsenosides. They are specific with respect to the nature of the glycosidic linkage, the position and the order in which the linkages are cleaved. Ginsenoside Rb1 β-glucosidase specifically and sequentially hydrolyses the 20-[β-D-glucopyranosyl-(1?6)-β-D glucopyranosyloxy] residues attached to position 20 by first hydrolysing the (1?6)-glucosidic bond to generate ginsenoside Rd as an intermediate, followed by hydrolysis of the remaining 20-O-β-D-glucosidic bond. Group: Enzymes. Enzyme Commission Number: EC 3.2.1.192. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3876; ginsenoside Rb1 β-glucosidase; EC 3.2.1.192. Cat No: EXWM-3876. Creative Enzymes
Ginsenoside Rb2 Ginsenoside Rb2 is one of the main bioactive components of ginseng extracts. Rb2 can upregulate GPR120 gene expression. Ginsenoside Rb2 has antiviral effects. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Cream-white powder. CAS No. 11021-13-9. Molecular formula: C53H90O22. Mole weight: 1079.27. Purity: 0.98. IUPACName: (2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-6-methyl-2-[(2S,3R,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol. Canonical SMILES: CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C. Product ID: ACM11021139. Alfa Chemistry — ISO 9001:2015 Certified. Categories: Ginsenoside Rb1. Alfa Chemistry.
Ginsenoside Rb2 Ginsenoside Rb2. Group: Biochemicals. Alternative Names: Ginsenoside. Grades: Plant Grade. CAS No. 11021-13-9. Pack Sizes: 20mg. Molecular Formula: C53H90O22, Molecular Weight: 1079.27. US Biological Life Sciences. USBiological 9
Worldwide
Ginsenoside Rb2 analytical standard. Group: Herbal medicinal products standards. Alfa Chemistry Analytical Products
Ginsenoside Rb2 Ginsenoside Rb2 is one of the main bioactive components of ginseng extracts. Rb2 can upregulate GPR120 gene expression. Ginsenoside Rb2 has antiviral effects. Uses: Scientific research. Group: Natural products. Alternative Names: Ginsenoside C. CAS No. 11021-13-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0040. MedChemExpress MCE
Ginsenoside Rb3 analytical standard. Group: Herbal medicinal products standards. Alfa Chemistry Analytical Products
Ginsenoside Rb3 Ginsenoside Rb3. Group: Biochemicals. Alternative Names: Gypenoside IV. Grades: Plant Grade. CAS No. 68406-26-8. Pack Sizes: 10mg. Molecular Formula: C53H90O22, Molecular Weight: 1079.27. US Biological Life Sciences. USBiological 9
Worldwide

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