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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. Group: Natural products. Alternative Names: Ginsenoside B2; Panaxoside Re; Sanchinoside Re. CAS No. 52286-59-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 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
Korean Red Ginseng P.E. 10% Ginsenoside
Korean Red Ginseng P.E. 10% Ginsenoside.
CA, FL & NJ
20-O-multi-glycoside ginsenosidase
The 20-O-multi-glycoside ginsenosidase catalyses the hydrolysis of the 20-O-α-(1?6)-glycosidic bond and the 20-O-β-(1?6)-glycosidic bond of protopanaxadiol-type ginsenosides. The enzyme usually leaves a single glucosyl residue attached at position 20, although it can cleave the remaining glucosyl residue with a lower efficiency. Starting with a ginsenoside that is glycosylated at positions 3 and 20, such as ginsenosides Rb1, Rb2, Rb3 and Rc, the most common product is ginsenoside Rd, with a low amount of ginsenoside Rg3 also formed. Group: Enzymes. Synonyms: ginsenosidase type II (erroneous). Enzyme Commission Number: EC 3.2.1.195. 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-3879; 20-O-multi-glycoside ginsenosidase; EC 3.2.1.195; ginsenosidase type II (erroneous). Cat No: EXWM-3879.
20(R)Ginsenoside rg3
20(R)Ginsenoside rg3. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ginsenoside Rg3 (R-); 20(S)-ginsenoside Rg3; R-form-Ginsenoside Rg3; Ginsenoside Rg3 Rh2; (2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[[(10R,12S,13R,14R,17S)-12-hydroxy-17-[(1R)-1-hydroxy-1,5-dimethyl-hex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-methylol-tetrahydropyran-3-yl]oxy-6-methylol-tetrahydropyran-3,4,5-triol. Appearance: white powder. CAS No. 38243-03-7. Molecular formula: C42H72O13. Mole weight: 785.01. Purity: 98%+. IUPACName: (2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(2S)-2-[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-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]oxyoxan-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)COC6C(C(C(CO6)O)O)O)O)O)O)C)C)O)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C. Density: 1.3. Product ID: ACM38243037. Alfa Chemistry ISO 9001:2015 Certified.
(20R)-Ginsenoside Rg3
Ginsenoside Rg3 is extracted from the roots of Panax ginseng C. A. Mey. It could enhance immunity and the ability of antivirus and infection. It also could protect hematopoietic function of marrow, improve the ability of hepatic detoxifcatio and promote restoration of hepatic tissue. It prevents and treats coronary heart disease, climacteric syndrome, diabetes, anemia. Synonyms: beta-D-Glucopyranoside,(3beta,12beta)-12,20-dihydroxydammar-24-en-3-yl 2-O-beta-D-glucopyranosyl; 20(R)-Propanaxadiol; (2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[[(10R,12S,13R,14R,17S)-12-hydroxy-17-[(1R)-1-hydroxy-1,5-dimethyl-hex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-methylol-tetrahydropyran-3-yl]oxy-6-methylol-tetrahydropyran-3,4,5-triol. Grades: >98%. CAS No. 38243-03-7. Molecular formula: C42H72O13. Mole weight: 785.01.
20(R)-Ginsenoside Rg3-d6
20(R)-Ginsenoside Rg3-d6 is the labelled version of 20(R)-Ginsenoside Rg3, which causes an inhibition of phosphatidylinositol 3-kinase/Akt activation that, in turn, results in modulations in Bcl-2 family proteins in such a way that the apoptosis of U87 cells are regulated, relating to in vivo inhibition of tumor angiogenesis of lung cancer. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C42H66D6O13, Molecular Weight: 791.05. US Biological Life Sciences.
Worldwide
20(R)-Ginsenoside Rh2
20(R)-Ginsenoside Rh2, a matrix metalloproteinase (MMP) inhibitor, acts as a cell antiproliferator. It has anticancer effects via blocking cell proliferation and causing G1 phase arrest. 20(R)-Ginsenoside Rh2 induces apoptosis, and has anti-inflammatory and antioxidative activity. 20(R)-Ginsenoside Rh2 inhibits the replication and proliferation of mouse and human gammaherpesvirus 68 (MHV-68) with an IC50 of 2.77 μM for murine MHV-68. Uses: Designed for use in research and industrial production. Additional or Alternative Names: b-D-Glucopyranoside, (3b,12b,20R)-12,20-dihydroxydammar-24-en-3-yl; (3beta,12beta)-12,20-dihydroxydammar-24-en-3-yl beta-d-glucopyranoside; 20-(R)-Ginsenoside Rh2; 20(R)-Ginsenoside Rh2; 20(R)-GINSENOSIDERH2; Ginsenoside-Rh2; Ginsenoside Rh2, 20(R)-; 20(R)-Ginsenoside-Rh2; (R) Ginsenoside Rh2. Product Category: Inhibitors. Appearance: Powder. CAS No. 112246-15-8. Molecular formula: C36H62O8. Mole weight: 622.88. Purity: 0.98. IUPACName: (2R,3R,4S,5S,6R)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-17-[(2R)-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)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)O)C)C)O)C)O)C. Product ID: ACM112246158. Alfa Chemistry ISO 9001:2015 Certified.
20(S)-Ginsenoside F2
Ginsenoside F2 is a bioactive metabolite of the ginsenoside component of Panax ginseng with the ability to regulate element-binding protein cleavage activating protein and transforming growth factor- β pathways. This control over apoptosis can lead to a control over hair growth and hair loss in mammals. Group: Biochemicals. Grades: Highly Purified. CAS No. 62025-49-4. Pack Sizes: 10mg, 100mg. Molecular Formula: C42H72O13. US Biological Life Sciences.
Worldwide
20(S)-Ginsenoside Rg2
20(S)-Ginsenoside Rg2 is used as an aldose reductase inhibitor and my exert anti-inflammatory and immunomodulatory activity. It exists as a bioactive metabolite of the ginsenoside component of Panax ginseng. Group: Biochemicals. Grades: Highly Purified. CAS No. 52286-74-5. Pack Sizes: 50mg, 500mg. Molecular Formula: C42H72O13. US Biological Life Sciences.
Worldwide
20(S)-Ginsenoside Rh2
20(S)-Ginsenoside Rh2. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ginsenoside Rh2; (3β,12β)-12,20-Dihydroxydammar-24-en-3-yl-β-D-glucopyranoside; dihydroxydammar-24-en-3-yl; GinsenosideRh2; ginenoside Rh2. Appearance: White powder. CAS No. 78214-33-2. Molecular formula: C36H62O8. Mole weight: 622.87. Purity: 0.98. IUPACName: (2R,3R,4S,5S,6R)-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)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)O)C)C)O)C)O)C. Density: 1.19 g/cm³. Product ID: ACM78214332. Alfa Chemistry ISO 9001:2015 Certified.
(20S)-Protopanaxatriol
(20S)-Protopanaxatriol is a metabolite of ginsenoside. (20S)-Protopanaxatriol works through the glucocorticoid receptor (GR) and estrogen receptor (ER) , and is also a LXRα inhibitor. (20 S )-Protopanaxatriol shows a broad spectrum of antitumor effects [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: 20(S)-APPT; g-PPT. CAS No. 34080-08-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0835.
2-Cyclohexylethyl-4-O-(a-D-glucopyranosyl)-b-D-glucopyranoside, a glycoside derived from Panax ginseng's ginsenoside Rb1, is a multi-functional compound exhibiting promising pharmaco-therapeutic potential. It has garnered significant attention due to its manifold biological activities involving neuroprotection, anti-cancer and anti-diabetic effects, which are relevant for the effective management of degenerative disorders such as Alzheimer's disease and type 2 diabetes. Synonyms: 2-Cyclohexylethyl-b-D-maltoside. CAS No. 260804-65-7. Molecular formula: C20H36O11. Mole weight: 452.49.
5,6-dehydrogensenoside Rd
5,6-dehydrogensenoside Rd, a triterpenoid reference standard, is a protopanaxadiol isolated from ginsenosides. Protopanaxadiol has been studied to have broad physiological activities, especially the antitumor biological activity. Synonyms: (3beta,12beta)-20-(beta-d-glucopyranosyloxy)-12-hydroxydammara-5,24-dien-3-yl 2-o-beta-d-glucopyranosyl-beta-d-glucopyranoside. Grades: > 98%. CAS No. 1268459-68-2. Molecular formula: C48H80O18. Mole weight: 945.15.
American ginseng extract
American ginseng extract. Applications: Applied in the food field, applied in the health product field;applied in the pharmaceutical field. Group: Others. Purity: 10%-80% Ginsenosideds UV. Appearance: Brown yellow powder. Source: American ginseng (Panax quinquefolius) is a herbaceous perennial plant in the ivy family. American ginseng was formerly particularly widespread in the Appalachian and Ozark regions (and adjacent forested regions such as Pennsylvania, New York and Ontario). It is also grown commercially, under artificial shade, woods cultivated, or wild-simulated methods, in Wisconsin and Minnesota. Wisconsin, particularly Marathon County, accounts for about 95% of production in the United States. It is also widely grown in Ontario, Canada and China. American ginseng extract. Cat No: EXTC-171.
Asian Ginseng Extract (Standard)
Ginseng Extract is extracted from the root and leaf of Panax ginseng C. A. Mey, which is the specie of slow-growing perennial plants with fleshy roots, belonging to the genus Panax of the family Araliaceae. Ginseng is found only in the northern hemisphere, in eastern Asia (mostly Korea, northeastern China, Bhutan and eastern Siberia), typically in cooler climates. Applications: 1.ginseng extract to alleviate motion sickness, pregnancy, post-operative nausea and vomiting2.mainly suitable for coronary heart disease, angina pectoris, heart rate is too slow, too fast, premature ventricular bo, blood pressure disorder, neurasthenia, menopausal syndrome. Group: Others. CAS No. Gins...oside Rb1: 41753-43-9Ginsenoside Rb2: 11021-13-9Ginsenoside Re: 52286-59-6Ginsenoside Rc: 11021-14-0Ginsenoside Rf: 52286-58-5. Purity: 10.0%-80.0% Ginsenoside UV. Mole weight: Ginsenoside Rg1: 801.01Ginsenoside Rb1: 1109.29Ginsenoside Rb2: 1079.26Ginsenoside Re: 947.15Ginsenoside Rc: 1079.26Ginsenoside Rf: 801.01. Asian Ginseng Extract (Standard); Ginsenoside Rg1: 22427-39-0Ginsenoside Rb1: 41753-43-9Ginsenoside Rb2: 11021-13-9Ginsenoside Re: 52286-59-6Ginsenoside Rc: 11021-14-0Ginsenoside Rf: 52286-58-5; Ginsenoside Rg1: C42H72O14Ginsenoside Rb1: C54H92O23Ginsenoside Rb2: C53H90O22Ginsenoside Re: C48H82O18Ginsenoside Rc: C53H90O22Ginsenoside Rf: C42H72O14. Cat No: EXTW-020.
b-D-Glucopyranoside,(3b,12b)-20-[(6-O-a-L-arabinopyranosyl-b-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl2-O-b-D-glucopyranosyl-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ginsenoside C, Ginsenoside Rb2, gingenoside C, EINECS 234-251-4, NSC 308878, CID73598, C53H90O22, LS-71499, 20-((6-O-alpha-L-Arabinopyranosyl-beta-D-glucopyranosyl)oxy)-12beta-hydroxydammar-24-en-3beta-yl 2-O-beta-D-glucopyranosyl-beta-D-glucopyranoside, beta-D-Glucopyranoside, (3-beta,12-beta)-20-((6-O-alpha-L-arabinopyranosyl-beta-D-glucopyranosyl)oxy)-12-hydroxydammar-24-en-3-yl 2-O-beta-D-glucopyranosyl-, 11021-13-9, 52351-30-1, 52590-95-1, 75139-47-8. Product Category: Heterocyclic Organic Compound. CAS No. 75139-47-8. Molecular formula: C53H90O22. Mole weight: 1079.2685. Purity: 0.96. 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-. Canonical SMILES: CC1CC2=NN=C(N2C3=CC=CC=C3N1)C. Density: 1.42 g/cm³. Product ID: ACM75139478. Alfa Chemistry ISO 9001:2015 Certified.
β-amyrin 28-monooxygenase
The enzyme, found in plants, is involved in the biosynthesis of oleanane-type triterpenoids, such as ginsenoside Ro. The enzyme from Medicago trunculata (CYP716A12) can also convert α-amyrin and lupeol to ursolic acid and betulinic acid, respectively. Group: Enzymes. Synonyms: CYP716A52v2; CYP716A12; β-amyrin 28-oxidase. Enzyme Commission Number: EC 1.14.13.201. 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-0803; β-amyrin 28-monooxygenase; EC 1.14.13.201; CYP716A52v2; CYP716A12; β-amyrin 28-oxidase. Cat No: EXWM-0803.
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.
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 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 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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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: Designed for use in research and industrial production. Additional or Alternative Names: [20-[(6-O-α-L-Arabinofuranosyl-β-D-glucopyranosyl)oxy]-12β-hydroxydammar-24-en-3β-yl]2-O-β-D-glucopyranosyl-β-D-glucopyranoside. Product Category: Inhibitors. Appearance: White powder. CAS No. 11021-14-0. Molecular formula: C53H90O22. Mole weight: 1079.27. Purity: 0.98. IUPACName: (2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-methylhept-5-en-2-yl]-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-3-yl]oxy]-4,5-dihydroxy-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@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO[C@H]8[C@@H]([C@H]([C@@H](O8)CO)O)O)O)O)O)C. Density: 1.42±0.1 g/ml. Product ID: ACM11021140. Alfa Chemistry ISO 9001:2015 Certified. Categories: Ginsenoside Rb1.
Ginsenoside Rc
Ginsenoside Rc, one of major Ginsenosides from Panax ginseng , enhances GABA receptor A ( GABA A )-mediated ion channel currents (I GABA ). Ginsenoside Rc inhibits the expression of TNF-α and IL-1&beta. Uses: Scientific research. Group: Natural products. Alternative Names: Panaxoside Rc. CAS No. 11021-14-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N0042.
Ginsenoside Rd
Ginsenoside Rd inhibits TNFα-induced NF-κB transcriptional activity with an IC 50 of 12.05±0.82 μM in HepG2 cells. Ginsenoside Rd inhibits expression of COX-2 and iNOS mRNA. Ginsenoside Rd also inhibits Ca 2+ influx. Ginsenoside Rd inhibits CYP2D6 , CYP1A2 , CYP3A4 , and CYP2C9 , with IC 50 s of 58.0±4.5 μM, 78.4±5.3 μM, 81.7±2.6 μM, and 85.1±9.1 μM, respectively. Uses: Scientific research. Group: Natural products. Alternative Names: Gypenoside VIII. CAS No. 52705-93-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0043.
Ginsenoside Rd2
Ginsenoside Rd2 is a composition of roots of Panax ginseng. Ginsenoside Rd is a primary constituent of the ginseng rhizome and the administration of ginsenoside Rd significantly increased the reduced GSHPx and glutathione reductase activity. Synonyms: β-D-Glucopyranoside, (3β,?12β)?-3-(β-D-glucopyranosyloxy)?-12-hydroxydammar-24-en-20-yl 6-O-α-L-arabinopyranosyl-; (3β,12β)-3-(β-D-Glucopyranosyloxy)-12-hydroxydammar-24-en-20-yl 6-O-α-L-arabinopyranosyl-β-D-glucopyranoside; 3-O-Glucosylginsenoside C Y; 3-O-β-D-Glucopyranosylginsenoside C-Y; Ginsenoside C-O. Grades: > 98%. CAS No. 83480-64-2. Molecular formula: C47H80O17. Mole weight: 917.13.
Ginsenoside Rf
Ginsenoside Rf, extracted from the traditional Chinese herb ginseng, is a novel natural anticancer products known for its favorable safety and efficacy profiles. It inhibits Ca2+ channels in mammalian sensory neurons through a mechanism requiring G-proteins, whereas a variety of other ginsenosides were relatively ineffective. It might be useful in itself or as a template for designing additional modulators of neuronal Ca2+ channels. It induces G2/M phase cell cycle arrest and apoptosis in human osteosarcoma MG-63 cells through the mitochondrial pathway. Uses: Anti-arthritic agent. Synonyms: (3b,6a,12b)-3,12,20-Trihydroxydammar-24-en-6-yl-2-O-(b-D-glucopyranosyl)-b-D-glucopyranoside. Grades: >98%. CAS No. 52286-58-5. Molecular formula: C42H72O14. Mole weight: 801.03.
Ginsenoside Rf
Ginsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca 2+ channel. Uses: Scientific research. Group: Natural products. Alternative Names: Panaxoside Rf. CAS No. 52286-58-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0601.
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. Group: Natural products. Alternative Names: Panaxoside A; Panaxoside Rg1. CAS No. 22427-39-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N0045.
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. Categories: Niosomes, ethosomes, and transfersomes.
Ginsenoside Rg2
Ginsenoside Rg2, a steroid glycosides, is abundant in Panax ginseng root, which has been used for prevention of illness. It has a neuroprotective effect against glutamate-induced neurotoxicity through mechanisms related to anti-oxidation and anti-apoptosis. It inhibits nicotinic acetylcholine receptor-mediated Na+ influx and channel activity. It might regulate the 5-HT3A receptors that are expressed in Xenopus oocytes. It may have properties that inhibit or prevent the growth of tumors. Ginsenoside Rg2 can be used in health products. Uses: Anti-arthritic agent. Synonyms: (3b,6a,12b)-3,12,20-Trihydroxydammar-24-en-6-yl 2-O-(6-deoxy-a-L-mannopyranosyl)-b-D-glucopyranoside; β-D-Glucopyranoside, (3β,6α,12β)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-; Dammarane, β-D-glucopyranoside deriv.; Chikusetsusaponin I. Grades: >98%. CAS No. 52286-74-5. Molecular formula: C42H72O13. Mole weight: 785.01.
Ginsenoside Rg2
Ginsenoside Rg2 is one of the major active components of ginseng. Ginsenoside Rg2 inhibits VCAM-1 and ICAM-1 expressions stimulated with lipopolysaccharide (LPS). Ginsenoside Rg2 also reduces Aβ 1-42 accumulation. Uses: Scientific research. Group: Natural products. Alternative Names: Chikusetsusaponin I; Panaxoside Rg2; Prosapogenin C2. CAS No. 52286-74-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N0602.
Ginsenoside Rg3
Ginsenoside Rg3. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (3β,12β)-12,20-Dihydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside. Appearance: White to beige powder. CAS No. 14197-60-5. Molecular formula: C42H72O13. Mole weight: 785.03. Purity: 0.98. IUPACName: (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. Density: 1.3 g/ml. Product ID: ACM14197605. Alfa Chemistry ISO 9001:2015 Certified. Categories: Ginsenoside Rg1.
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. Categories: Niosomes, ethosomes, and transfersomes.
Ginsenoside Rg5
Ginsenoside Rg5, a main constituent isolated from red ginseng, exhibits anti-inflammatory property as in LPS-stimulated alveolar macrophages it inhibited the expression of proinflammatory cytokines including IL-1β and TNF-α, as same as inflammatory enzyme. Synonyms: β-D-Glucopyranoside, (3β,12β,20E)-12-hydroxydammara-20(22),24-dien-3-yl 2-O-β-D-glucopyranosyl-; (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-4,4,8,10,14-pentamethyl-17-((E)-6-methylhepta-2,5-dien-2-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; (3β,12β,20E)-12-Hydroxydammara-20(22),24-dien-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside; Ginsenoside Rg5E. Grades: >98%. CAS No. 186763-78-0. Molecular formula: C42H70O12. Mole weight: 767.00.
Ginsenoside Rg6
Ginsenoside Rg6 inhibits TNF-α-induced NF-κB transcriptional activity with an IC 50 of 29.34 μM in HepG2 cells. Ginsenoside Rg6 also exhibits apoptosis -inducing effect. Uses: Scientific research. Group: Natural products. CAS No. 147419-93-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N0907.
Ginsenoside Rh1
Ginsenoside Rh1 (Prosapogenin A2) inhibits the expression of PPAR-γ, TNF-α, IL-6, and IL-1β. Uses: Designed for use in research and industrial production. Additional or Alternative Names: β-D-Glucopyranoside, (3β,6α,12β)-3,12,20-trihydroxydammar-24-en-6-yl. Product Category: Inhibitors. Appearance: Powder. CAS No. 63223-86-9. Molecular formula: C36H62O9. Mole weight: 638.88. Purity: 0.98. IUPACName: (2R,3R,4S,5S,6R)-2-[[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-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-6-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(C[C@@H]([C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)C)O)C)O)C. Density: 1.23 g/ml. Product ID: ACM63223869. Alfa Chemistry ISO 9001:2015 Certified. Categories: Ginsenoside Rb1.
Ginsenoside Rh1
Ginsenoside Rh1 (Prosapogenin A2) inhibits the expression of PPAR-γ , TNF-α , IL-6 , and IL-1&beta. Uses: Scientific research. Group: Natural products. Alternative Names: Prosapogenin A2; Sanchinoside B2; Sanchinoside Rh1. CAS No. 63223-86-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N0604.
Ginsenoside Rh2
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. Group: Natural products. Alternative Names: 20(S)-Ginsenoside Rh2; 20(S)-Rh2; Ginsenoside-Rh2. CAS No. 78214-33-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0605.
Ginsenoside Rh3
Ginsenoside Rh3 is a bacterial metabolite of Ginsenoside Rg5. Ginsenoside Rh3 treatment in human retinal cells induces Nrf2 activation. Uses: Scientific research. Group: Natural products. CAS No. 105558-26-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N0606.
Ginsenoside Rh3
Ginsenoside Rh3 is isolated from red ginseng and metabolized from ginsenoside Rg5. It can be anti-inflammatory. Uses: Ginsenoside rh3 is isolated from red ginseng and could be used as an anti-inflammatory agent. Synonyms: [(20Z)-12β-Hydroxy-5α-dammara-20(22),24-dien-3β-yl]β-D-glucopyranoside; (3β, 12β,20Z)-12-Hydroxydammara-20(22),24-dien-3-yl-β-D-glucopyranoside. Grades: >98%. CAS No. 105558-26-7. Molecular formula: C36H60O7. Mole weight: 604.86.
Ginsenoside Rh4
Ginsenoside Rh4 is a rare saponin obtained from Panax notoginseng. Ginsenoside Rh4 activates Bax , caspase 3 , caspase 8 , and caspase 9. Ginsenoside Rh4 also induces autophagy. Uses: Scientific research. Group: Natural products. CAS No. 174721-08-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0905.
Ginsenoside Rh7
Ginsenoside Rh7 is a new dammarane-type triterpene saponins from the Leaves of Panax ginseng. Panax ginseng is an ancient and famous herbal drug in traditional chinese medicines. Bioactive saponins from natural medicines, a number of dammarane-type triterpene oligoglycosides were found to have anti-cancer, anti-arrhythmia and inhibitory effects on reducing sideeffects of steroid hormones. Synonyms: β-D-Glucopyranoside, (3β,?7β,?12β)?-3,?7,?12-trihydroxydammara-5,?24-dien-20-yl; (3β,7β,12β)-3,7,12-Trihydroxydammara-5,24-dien-20-yl β-D-glucopyranoside. Grades: > 98%. CAS No. 343780-68-7. Molecular formula: C36H60O9. Mole weight: 636.86.
Ginsenoside Rh8
Ginsenoside Rh8 is a saponin composition of roots of Panax ginseng. Ginsenoside-Rh8 was also obtained as a white powder. Ginsenosides are the primary bioactive components of Asian ginseng and more than 30 ginsenosides were reported from ginseng so far. Ginsenosides Rbl, Rb2, Rc, Rd, Rgl, Rg2, and Re are major constituents of white and red ginsengs, while ginsenosides Rg3, Rgs, and Rg6 are known to be unique constituents of red ginseng. Synonyms: Dammar-24-en-12-one, 20-(β-D-glucopyranosyloxy)-3,6-dihydroxy-, (3β,?6α)-; (3β,6α)-20-(β-D-Glucopyranosyloxy)-3,6-dihydroxydammar-24-en-12-one. Grades: > 98%. CAS No. 343780-69-8. Molecular formula: C36H60O9. Mole weight: 636.86.
Ginsenoside Rk1
Ginsenoside Rk1 is a unique component created by processing the ginseng plant (mainly Sung Ginseng, SG) at high temperatures [1]. Ginsenoside Rk1 has anti-inflammatory effect, suppresses the activation of Jak2/Stat3 signaling pathway and NF-κB [2]. Ginsenoside Rk1 has anti-tumor effect, antiplatelet aggregation activities, anti-insulin resistance, nephroprotective effect, antimicrobial effect, cognitive function enhancement, lipid accumulation reduction and prevents osteoporosis [1]. Ginsenoside Rk1 induces cell apoptosis by triggering intracellular reactive oxygen species ( ROS ) generation and blocking PI3K/Akt pathway [3]. Uses: Scientific research. Group: Natural products. CAS No. 494753-69-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 20 mg. Product ID: HY-N2515.
Ginsenoside Rk2
Ginsenoside Rk2 is a new dammarane glycosides isolated from the processed ginseng. Ginseng (Panax ginseng C. A. Meyer, Araliaceae) is one of the most popular herbal medicines in the Orient. The most well known chemical constituent of ginseng is ginsenoside, which is a dammarane glycoside. More than 30 ginsenosides were reported from ginseng so far. Synonyms: (3β,12β)-12-Hydroxydammara-20,24-dien-3-yl β-D-glucopyranoside; 3β,12β-Dihydroxydammar-20(21),24-diene-3-O-β-D-glucopyranoside; PAN 20. Grades: > 98%. CAS No. 364779-14-6. Molecular formula: C36H60O7. Mole weight: 604.86.
Gynostemma Extract
Gynostemma Extract (Ginsenoside C-Mx1) is a natural product. Uses: Scientific research. Group: Natural products. Alternative Names: Ginsenoside C-Mx1; Gypenoside IX. CAS No. 80321-63-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0167.
Notoginsenoside R4
Notoginsenoside R4 is a ginsenoside that can be isolated from ginseng roots. In the molecular docking results, Notoginsenoside R4 can target STAT3, AKT1, HRAS, VEGFA and CASP3 [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 87741-77-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N10336.
Panax Notoginseng Extract
Panax notoginseng extract is prepared from the species of the genus Panax, also known as sanqi extract powder. Panax notoginseng extract powder contain high potency notoginsenoside, Ginsenoside Rb1, Ginsenoside Rg1, Ginsenoside Rd, Ginsenoside Re, and Ginsenoside Rb2, which are most active ingredients impacting on your overall health and nutritionally support healthy heart function, blood circulation, and performance. Group: Others. Mole weight: 933.14. Panax Notoginseng Extract; Panax Pseudo-Ginseng Wall. Var. Cat No: EXTC-016.
Pseudoginsenoside F11
Pseudoginsenoside F11 (Ginsenoside A1), a component of Panax quinquefolium (American ginseng), has been demonstrated to antagonize the learning and memory deficits induced by scopolamine, morphine and methamphetamine in mice. Uses: Scientific research. Group: Natural products. Alternative Names: Ginsenoside A1. CAS No. 69884-00-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N0541.
Selected Plant-Sourced Compound Library
A unique collection of 2720 plant-sourced compounds; - All are in preclinical or clinical research phases with the most research potential; - Includes many popular natural products, such as Artemisinin, Ginsenoside, etc. ; - Structurally diverse, medicinally active, and cell permeable; - Detailed compound information with structure, target, activity, IC50 value, and biological activity description; - NMR and HPLC/LCMS validated to ensure high purity and quality. Uses: Scientific use. Product Category: L4600. Categories: Selected Plant-Sourced Compounds Libraries.
Chinese Ginseng(Panax Ginseng) Root 10% Ginsenosides HPLC
Chinese Ginseng(Panax Ginseng) Root 10% Ginsenosides HPLC. Categories: glycyl-l-histidyl-l-lysine; 49557-75-7.
CA, FL & NJ
Ginseng Ginsenosides Mix
100 ?g/mL each component in methanol, ampule of 100 ?g/mL, certified reference material. Group: Herbal medicinal products standards.