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| Product | Description | |
|---|---|---|
| Ginkgolide B | Ginkgolide B is a PAFR antagonist with an IC50 of 3.6 μM. Ginkgolide B is a bioactive diterpenoid trilactone derived from Ginkgo biloba leaves, known for its potent platelet-activating factor (PAF) antagonism. It has a complex structure with multiple chiral centers and exhibits significant neuroprotective and cerebrovascular benefits. These properties make it a promising candidate for treating neurodegenerative diseases, inflammation, and conditions related to cerebral blood flow. Uses: Fibrinolytic agents. Synonyms: (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; 5H-Dicyclopenta[b,c]furan-3,5a(6H)-diacetic acid, 6-tert-butyl-3a-carboxyhexahydro-α5a,1,2,3,5,8-hexahydroxy-α3-methyl-, tri-γ-lactone; Ginkgolide A, 1-hydroxy-, (1β)-; 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, 3-(1,1-dimethylethyl)hexahydro-4,7b,11-trihydroxy-8-methyl-, [1R-(1α,3β,3aS*,4β,6aα,7aα,7bα,8α,10aα,11β,11aR*)]-; Bilobalide B; BN 52021; BN 52051; Ginkgolides, ginkgolide B. Grade: >98%. CAS No. 15291-77-7. Molecular formula: C20H24O10. Mole weight: 424.40. |  |
| 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. |  Worldwide |
| 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. Category: Signaling pathways. Alternative Names: BN-52021. CAS No. 15291-77-7. Pack Sizes: 10 mM * 1 mL in DMSO; 25 mg; 50 mg; 100 mg. Product ID: HY-N0784. |  |
| Ginkgolide C | Ginkgolide C is a bioactive diterpenoid trilactone compound derived from the leaves of the Ginkgo biloba tree. Similar to its counterparts Ginkgolide A and Ginkgolide B, it is characterized by its unique trilactone structure with multiple chiral centers, contributing to its diverse pharmacological properties. Ginkgolide C is known for its potent antagonistic effects on platelet-activating factor (PAF), making it a promising candidate for treating inflammatory and allergic conditions. Additionally, it has been studied for its neuroprotective effects, particularly in the context of neurodegenerative diseases and cerebral ischemia. Synonyms: (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; 5H-Dicyclopenta[b,c]furan-3,5a(6H)-diacetic acid, 6-tert-butyl-3a-carboxyhexahydro-α5a,1,2,3,5,7,8-heptahydroxy-α3-methyl-, tri-γ-lactone; Ginkgolide A, 1,7-dihydroxy-, (1β,7β)-; 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, 3-(1,1-dimethylethyl)hexahydro-2,4,7b,11-tetrahydroxy-8-methyl-, [1R-(1α,2α,3β,3aS*,4β,6aα,7aα,7bα,8α,10aα,11α,11aR*)]-; BN 52022. Grade: >98%. CAS No. 15291-76-6. Molecular formula: C20H24O11. Mole weigh | |
| 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. | Worldwide |
| 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. | Worldwide |
| Ginkgolide K | Ginkgolide K is extracted from the leaves of Ginkgo biloba L. It promotes angiogenesis after ischemia stroke and promotes astrocyte migration and proliferation after oxygen-glucose deprivation. It improves nerve injury after cerebral ischemia-reperfusion and inhibits PAF-induced platelet aggregation. It also can promote the clearance of A53T mutation alpha-synuclein in SH-SY5Y cells and shows anti- Parkinson's disease activity. It shows neuroprotective effect and anti-oxidative stress on ischemic stroke. Synonyms: 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, 3-(1,1-dimethylethyl)-2,3,10a,11-tetrahydro-4,11-dihydroxy-8-methyl-, (1R,3S,3aS,4R,6aR,7aS,10aR,11R,11aR)-. Grade: 97.5%. CAS No. 153355-70-5. Molecular formula: C20H22O9. Mole weight: 406.38. | |
| Ginkgolide K | Ginkgolide K, isolated from Ginkgo biloba, induces protective autophagy through the AMPK/mTOR/ULK1 signaling pathway. Ginkgolide K possesses neuroprotective activity[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 153355-70-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-N4176. | |
| Ginkgoneolic acid | Ginkgoneolic acid. Group: Biochemicals. CAS No. 20261-38-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ginkgoneolic acid | Ginkgoneolic acid. Alternative Names: 2-Hydroxy-6-tridecyl-benzoic acid. CAS No. 20261-38-5. Purity: >95.0%. Product ID: FFC-AR-20261385. Molecular formula: C20H32O3. Mole weight: 320.47. IUPAC Name: 2-hydroxy-6-tridecylbenzoic acid. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| 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. |  |
| Ginseng Extract (Ratio) | Ginseng Extract (Ratio). Group: Others. Purity: 4:1~20:1. Ginseng Extract (Ratio). Cat No: EXTW-035. | |
| 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. | |
| 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. | |
| 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. | |
| 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. | 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 μM and 63.6±4.2 μM, respectively. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ginsenoside compound K; Ginsenoside K. CAS No. 39262-14-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0904. | |
| Ginsenoside C-K | Ginsenoside C-K is an intestinal microbiota metabolite of ginsenoside Rb1, which possesses anti-proliferative and anti-inflammatory activities. Synonyms: Ginsenoside K. Grade: >98%. CAS No. 39262-14-1. Molecular formula: C36H62O8. Mole weight: 622.87. | |
| Ginsenoside Compound K | Ginsenoside Compound K. Alternative Names: Compound K; Ginsenoside K; X1141; N1890. CAS No. 39262-14-1. Purity: 98%. Product ID: ACM39262141. Molecular formula: C36H62O8. Mole weight: 622.88. IUPAC Name: (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. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Ginsenoside F1 | Ginsenoside F1. Alternative Names: 3β,6α,12β-Trihydroxy-5α-dammar-24-en-20-yl β-D-glucopyranoside. CAS No. 53963-43-2. Purity: 98%. Product ID: ACM53963432-1. Molecular formula: C36H62O9. Mole weight: 638.87. IUPAC Name: (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. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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. Category: Signaling pathways. Alternative Names: 20(S)-Ginsenoside F1. CAS No. 53963-43-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0598. | |
| 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. | Worldwide |
| Ginsenoside F1 | Ginsenoside F1, a metabolite of ginsenoside Rg1, is reported to be antiaging and antioxidative, and to have beneficial effects on skin. It significantly reduced ultraviolet-B-induced cell death and protected HaCaT cells from apoptosis caused by ultraviolet B irradiation. Uses: A metabolite of ginsenoside rg1. Synonyms: (20S)-20-(β-D-Glucopyranosyloxy)dammar-24-ene-3β,6α,12β-triol; 3β,6α,12β-Trihydroxy-5α-dammar-24-en-20-yl β-D-glucopyranoside; (3b,6a,12b)-3,6,12-Trihydroxydammar-24-ene-20-yl beta-D-glucopyranoside; 20(S)-Ginsenoside F1; Panaxoside Aprogenin. Grade: >98%. CAS No. 53963-43-2. Molecular formula: C36H62O9. Mole weight: 638.87. | |
| Ginsenoside F2 | Ginsenoside F2 is extracted from the root of Panax ginseng C. A. Mey. It was assessed for its antiproliferative activity against breast cancer stem cells (CSCs). It induced apoptosis in breast CSCs by activating the intrinsic apoptotic pathway and mitochondrial dysfunction. It decreased the expression of TGF-β2 and SCAP proteins. Synonyms: (20S)-3β,20-Bis(β-D-glucopyranosyloxy)-5α-dammar-24-ene-12β-ol; 12β-Hydroxy-5α-dammar-24-ene-3β,20-diylbis(β-D-glucopyranoside); 20(S)-Ginsenoside-F2. Grade: >98%. CAS No. 62025-49-4. Molecular formula: C42H72O13. Mole weight: 785.01. | |
| 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. | 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. | Worldwide |
| 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. | Worldwide |
| Ginsenoside Mb | Ginsenoside Mb. Group: Biochemicals. CAS No. 88105-29-7. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ginsenoside Ra1 | Ginsenoside Ra1 is a component from ginseng, inhibits protein tyrosine kinase (PTK) activation induced by hypoxia/reoxygenation[1]. Uses: Scientific research. Category: Natural products. CAS No. 83459-41-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N2506. | |
| 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. | Worldwide |
| Ginsenoside Rb1 | A major bioactive component of panax ginseng that promotes neurotransmitter release by modulating phosphorylation of synapsins through a cAMP-dependent protein kinase pathway. It has been reported to display immunostimulatory and anticancer effects. It has anti-aging effect, can be used in health products. Uses: Anti-oxidative damage,immunostimulatory,anticancer. Synonyms: β-D-Glucopyranoside, (3β,12β)-20-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-; (3β,12β)-20-[(6-O-β-D-Glucopyranosyl-β-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside; Arasaponin E1; Gynosaponin C; Gypenoside III; Notoginsenoside Rb1; NSC 310103; Panaxoside Rb1; RB 1; Sanchinoside E1; Sanchinoside Rb1. Grade: ≥95%. CAS No. 41753-43-9. Molecular formula: C54H92O23. Mole weight: 1109.32. | |
| 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: Scientific research. Category: Signaling pathways. Alternative Names: Gypenoside III. CAS No. 41753-43-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0039. | |
| 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. | |
| Ginsenoside Rb2 | Ginsenoside Rb2 is a 20(S)-protopanaxadiol glycoside extracted from ginseng. It shows potent antioxidant and anticancer biological activities. It inhibited invasiveness to the basement membrane of endometrial cancer cell lines Ishikawa. Uses: Ginsenoside rb2 is extracted from ginseng and could inhibit the tumor growth and metastasis by destructing the angiogenesis. Synonyms: (3b,12b)-20-[(6-O-a-L-Arabinopyranosyl-b-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-(b-D-glucopyranosyl)-b-D-glucopyranoside; Ginsenoside C. Grade: >98%. CAS No. 11021-13-9. Molecular formula: C53H90O22. Mole weight: 1079.30. | |
| 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. | Worldwide |
| 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. Category: Signaling pathways. Alternative Names: Ginsenoside C. CAS No. 11021-13-9. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0040. | |
| Ginsenoside Rb3 | Ginsenoside Rb3 is extracted from steamed Panax ginseng C. A. Meyer. Ginsenoside Rb3 exhibits inhibitory effect on TNFα-induced NF-κB transcriptional activity with an IC50 of 8.2 μM in 293T cell lines. Ginsenoside Rb3 also inhibits the induction of COX-2 and iNOS mRNA. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Gypenoside IV. CAS No. 68406-26-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0041. | |
| 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. | Worldwide |
| Ginsenoside-Rb3 | Ginsenoside Rb3 is a natural triterpenoid saponin. It has various pharmacological effects. It possesses the effect against isoproterenol-induced myocardial injury and heart function impairment, and that the mechanism of pharmacological action was related to the antioxidant activity of ginsenoside Rb3 at least in part. It could markedly protected OGD-Rep induced ischemic injury and the mechanisms maybe related to its suppression of the intracellular Ca2+ elevation and inhibition of apoptosis and caspase activity. It could be a promising candidate in the development of a novel class of anti-ischemic agent. Uses: Ginsenoside rb3 inhibits the upregulation of phospho-iκb-α and nuclear translocation of nf-κb subunit p65 induced by glucose deprivation then reperfusion. Synonyms: (3b,12b)-3-[(2-O-b-D-Glucopyranosyl-b-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 6-O-(b-D-glucopyranosyl)-b-D-glucopyranoside; Gypenoside IV. Grade: >98%. CAS No. 68406-26-8. Molecular formula: C53H90O22. Mole weight: 1079.27. | |
| Ginsenoside Rc | Ginsenoside Rc is a steroid glycoside, which is found exclusively in the plant genus Panax (ginseng). It has properties that inhibit or prevent tumors growth. It may have effects that prevent or limit the development of breast cancer. Uses: Ginsenoside rc is extracted from ginseng and has been found to be antioxidative, anti-aging and have sorts of other properties. Synonyms: (3b,12b)-20-[(6-O-a-L-Arabinofuranosyl-b-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-(b-D-glucopyranosyl)-b-D-glucopyranoside; Panaxoside Rc. Grade: >98%. CAS No. 11021-14-0. Molecular formula: C53H90O22. Mole weight: 1079.30. | |
| Ginsenoside Rc | Ginsenoside Rc. Group: Biochemicals. Grades: Plant Grade. CAS No. 11021-14-0. Pack Sizes: 20mg. Molecular Formula: C53H90O22, Molecular Weight: 1079.27. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rc | Ginsenoside Rc, one of major Ginsenosides from Panax ginseng, enhances GABA receptorA (GABAA)-mediated ion channel currents (IGABA). Ginsenoside Rc inhibits the expression of TNF-α and IL-1β. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Panaxoside Rc. CAS No. 11021-14-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-N0042. | |
| Ginsenoside Rd | Ginsenoside Rd. Group: Biochemicals. Alternative Names: Gypenoside VIII. Grades: Plant Grade. CAS No. 52705-93-8. Pack Sizes: 20mg. Molecular Formula: C48H82O18, Molecular Weight: 947.154. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rd | Ginsenoside Rd is a natural triterpenoid compound found in the roots of Panax ginseng C. A. Mey. Ginsenoside Re shows antioxidant activities. Uses: Antioxidant. Synonyms: (3b,12b)-20-(b-D-Glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl2-O-(b-D-glucopyranosyl)-b-D-glucopyranoside. Grade: >98%. CAS No. 52705-93-8. Molecular formula: C48H82O18. Mole weight: 947.18. | |
| ginsenoside Rd glucosyltransferase | The glucosyl group forms a 1?6 bond to the glucosyloxy moiety at C-20 of ginsenoside Rd. Isolated from sanchi ginseng (Panax notoginseng). Group: Enzymes. Synonyms: UDPG:ginsenoside Rd glucosyltransferase; UDP-glucose:ginsenoside Rd glucosyltransferase; UGRdGT. Enzyme Commission Number: EC 2.4.1.314. 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-2550; ginsenoside Rd glucosyltransferase; EC 2.4.1.314; UDPG:ginsenoside Rd glucosyltransferase; UDP-glucose:ginsenoside Rd glucosyltransferase; UGRdGT. Cat No: EXWM-2550. | |
| Ginsenoside Re | Ginsenoside Re is a natural triterpenoid compound found in the roots of Panax ginseng C. A. Mey. Ginsenoside Re shows effective antidiabetic activities via significant antioxidant efficacy, particularly in the prevention of diabetic microvasculopathy. Synonyms: β-D-Glucopyranoside, (3β,6α,12β)-20-(β-D-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-; (3β,6α,12β)-20-(β-D-Glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside; Chikusetsusaponin IV; Ginsenoside B2; Notoginsenoside Re; NSC 308877; Panaxoside Re; Re ginsenoside; Sanchinoside Re. Grade: >98%. CAS No. 52286-59-6. Molecular formula: C48H82O18. Mole weight: 947.18. | |
| Ginsenoside Re | Ginsenoside Re (Ginsenoside B2) is an extract from Panax notoginseng. Ginsenoside Re decreases the β-amyloid protein (Aβ). Ginsenoside Re plays a role in antiinflammation through inhibition of JNK and NF-κB. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ginsenoside B2; Panaxoside Re; Sanchinoside Re. CAS No. 52286-59-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-N0044. | |
| Ginsenoside Re | Ginsenoside Re. Group: Biochemicals. Grades: Plant Grade. CAS No. 52286-59-6. Pack Sizes: 20mg. Molecular Formula: C48H82O18, Molecular Weight: 947.15. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rf | Ginsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Panaxoside Rf. CAS No. 52286-58-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0601. | |
| Ginsenoside Rf | Ginsenoside Rf. Group: Biochemicals. Grades: Plant Grade. CAS No. 52286-58-5. Pack Sizes: 10mg. Molecular Formula: C42H72O14, Molecular Weight: 801.01. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rg1 | Ginsenoside Rg1 is one of the major active components of Panax ginseng. Ginsenoside Rg1 ameliorates the impaired cognitive function, displays promising effects by reducing cerebral Aβ levels. Ginsenoside Rg1 also reduces NF-κB nuclear translocation. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Panaxoside A; Panaxoside Rg1. CAS No. 22427-39-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0045. | |
| Ginsenoside Rg1 | Ginsenoside Rg1 is a natural triterpenoid isolated from the roots of Panax ginseng C. A. Mey. Ginsenoside Rg1 protects against arthitis through osteoclast differentiation inhibition. Ginsenoside Rg1 exhibits anti-inflammatory and anticancer activities. Ginsenoside Rg1 can be used in health products. Uses: Anti-inflammatory, anticancer. Synonyms: (3b,6a,12b)-3,12-Dihydroxydammar-24-ene-6,20-diyl bis-b-D-glucopyranoside; Panaxoside A; Ginsenoside A2; Sanchinoside C1. Grade: >98%. CAS No. 22427-39-0. Molecular formula: C42H72O14. Mole weight: 801.03. | |
| Ginsenoside Rg1 | Ginsenoside Rg1. Group: Biochemicals. Alternative Names: Ginsenoside A2; Panaxoside A; Sanchinoside C1. Grades: Plant Grade. CAS No. 22427-39-0. Pack Sizes: 20mg. Molecular Formula: C42H72O14, Molecular Weight: 801.013. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rg1 Liposome | Ginsenoside Rg1 is a monomeric saponin extracted from Panax notoginseng, belonging to the dammarane-type saponins. It exerts a protective effect on the learning and memory function of various dementia model animals. This product is a pre-formulated liposome encapsulating Ginsenoside Rg1. It is only for research purposes. Group: Drug-loaded liposome. |  |
| Ginsenoside Rg1 reference substance | Ginsenoside Rg1 reference substance. Uses: For analytical and research use. CAS No. 22427-39-0. Molecular formula: C42H72O14. Mole weight: 801.02. Catalog: APB22427390. |  |
| Ginsenoside Rg2 | Ginsenoside Rg2. Group: Biochemicals. CAS No. 52286-74-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rg2 (20(s)-Ginsenoside Rg2) | Ginsenoside Rg2 (20(s)-Ginsenoside Rg2). Group: Biochemicals. Alternative Names: Chikusetsusaponin I; Ginsenoside C. Grades: Plant Grade. CAS No. 52286-74-5. Pack Sizes: 20mg. Molecular Formula: C42H72O13, Molecular Weight: 785.013. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rg3 | Ginsenoside Rg3 is a natural product isolated from Panax ginseng. Similar to other ginsenosides it exhibits cardio protective effects. Ginsenoside Rg3 enhances cardiac, hERG (IKr) and KCNQ (Iks), channel currents by interaction with the channel pore entryway. It also inhibits the palmitate-induced apoptosis of MIN6N8 mouse insulinoma beta-cells through modulating p44/42 MAPK activation. Ginsenoside Rg3 also inhibits Aβ levels, NF-κB activity, and COX-2 expression. Synonyms: β-D-Glucopyranoside, (3β,12β)-12,20-dihydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-; (3β,12β)-12,20-Dihydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside; Dammar-24-ene-12β,20-diol, 3β-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-; (20S)-Propanaxadiol; (3β,12β)-12,20-Dihydroxydammar-24-en-3-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside; 20(S)-Ginsenoside-Rg3; 20(S)-Rg3; 20S-Ginsenoside Rg3; 3-O-β-D-Glucopyranosyl-(1→2)-β-D-glucopyranosyldammar-24-ene-3β,12β,20S-triol; Ginsenoside 20-Rg3; Ginsenoside Rg3s; S-Ginsenoside Rg3. Grade: >98%. CAS No. 14197-60-5. Molecular formula: C42H72O13. Mole weight: 785.01. | |
| Ginsenoside Rg3 | Ginsenoside Rg3. Alternative Names: (3β,12β)-12,20-Dihydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside. CAS No. 14197-60-5. Purity: 98%. Product ID: ACM14197605-1. Molecular formula: C42H72O13. Mole weight: 785.03. IUPAC Name: (2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-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. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Ginsenoside Rg3 (20(s)-Ginsenoside Rg3) | Ginsenoside Rg3 (20(s)-Ginsenoside Rg3). Group: Biochemicals. Grades: Plant Grade. CAS No. 14197-60-5. Pack Sizes: 20mg. Molecular Formula: C42H72O13, Molecular Weight: 785.01. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rg3 Liposome | Ginsenoside Rg3 is a compound extracted from Radix Ginseng that can promote apoptosis of tumor cells and inhibit tumor invasion, proliferation, and angiogenesis. This product is a pre-formulated liposome encapsulating Ginsenoside Rg3. It is only for research purposes. Group: Drug-loaded liposome. | |
| Ginsenoside Rg4 | Ginsenoside Rg4. Group: Biochemicals. Alternative Names: Ginsenoside F4. Grades: Plant Grade. CAS No. 126223-28-7. Pack Sizes: 5mg. Molecular Formula: C42H70O12, Molecular Weight: 766.998. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rg5 | Ginsenoside Rg5 is an aromatase inhibitor from Panax ginseng leaves. Also, it ameliorates cisplatin-induced nephrotoxicity in mice through inhibition of inflammation, oxidative stress, and apoptosis. Group: Biochemicals. Alternative Names: (3 β,12 β,20E)-12-hydroxydammara-20(22),24-dien-3-yl 2-O- β-D-glucopyranosyl- β-D-glucopyranoside. Grades: Highly Purified. CAS No. 186763-78-0. Pack Sizes: 1mg, 5mg, 10mg. Molecular Formula: C??H??O??, Molecular Weight: 767. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rg6 | Ginsenoside Rg6. Group: Biochemicals. Grades: Plant Grade. CAS No. 147419-93-0. Pack Sizes: 5mg. Molecular Formula: C42H70O12, Molecular Weight: 767. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rh1 | Ginsenoside Rh1. Group: Biochemicals. CAS No. 63223-86-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rh1 (20(s)-Ginsenoside Rh1) | Ginsenoside Rh1 (20(s)-Ginsenoside Rh1). Group: Biochemicals. Alternative Names: Sanchinoside B2. Grades: Plant Grade. CAS No. 63223-86-9. Pack Sizes: 20mg. Molecular Formula: C36H62O9, Molecular Weight: 638.871999999999. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rh2 | Ginsenoside Rh2 (20(S)-Ginsenoside Rh2) induces the activation of caspase-8 and caspase-9. Ginsenoside Rh2 induces cancer cell apoptosis in a multi-path manner. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 20(S)-Ginsenoside Rh2; 20(S)-Rh2. CAS No. 78214-33-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0605. | |
| Ginsenoside Rh2, 20(R)- | Ginsenoside Rh2, 20(R)-. Group: Biochemicals. CAS No. 112246-15-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rh2, 20(S)- | Ginsenoside Rh2, 20(S)-. Group: Biochemicals. CAS No. 78214-33-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ginsenoside Rh2 (20(s)-Ginsenoside Rh2) | Ginsenoside Rh2 (20(s)-Ginsenoside Rh2). Group: Biochemicals. Grades: Plant Grade. CAS No. 78214-33-2. Pack Sizes: 20mg. Molecular Formula: C36H62O8, Molecular Weight: 622.87. US Biological Life Sciences. | Worldwide |
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