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| Product | Description | |
|---|---|---|
| Ginkbilobin | Ginkbilobin is a novel antifungal protein from Ginkgo biloba seeds with sequence similarity to embryo-abundant protein. The protein, designated ginkbilobin, exerted potent antifungal activity against a variety of fungi, including Botrytis cinerea, Mycosphaerella arachidicola, Fusarium oxysporum, Rhizoctonia solani, and Coprinus comatus. Ginkbilobin exhibited a moderate antibacterial action against Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli. It suppressed the activity of HIV-1 reverse transcriptase and the proliferation of murine splenocytes. |  |
| Ginkgetin | Ginkgetin. Group: Biochemicals. Grades: Plant Grade. CAS No. 481-46-9. Pack Sizes: 10mg. Molecular Formula: C32H22O10, Molecular Weight: 566.51. US Biological Life Sciences. |  Worldwide |
| Ginkgetin | Ginkgetin Inhibitor. Uses: Scientific use. Product Category: T4S2126. CAS No. 481-46-9. |  |
| Ginkgetin | Ginkgetin, a biflavone, is isolated from Ginkgo biloba leaves. Ginkgetin exhibit anti-tumor, anti-inflammatory, neuroprotective, anti-fungal activities. Ginkgetin is also a potent inhibitor of Wnt signaling, with an IC50 of 5.92 μΜ[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 481-46-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0889. |  |
| Ginkgo biloba extract | Ginkgo biloba extract. CAS No. 90045-36-6. Product ID: CI-OT-0120. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Ginkgo Biloba Extract | Ginkgo biloba extract is prepared from the leaves of Maidenhair Tree after Adiantum, which is a unique species of tree with no close living relatives. Ginkgo biloba leaf extract is used for the treatment of numerous conditions, many of which are under scientific investigation. The most powerful effect of ginkgo biloba extract is on the circulating system. Ginkgo biloba extract can be used to treat respiratory problems such as asthma and bronchitis. Group: Others. Mole weight: 408.4. Ginkgo Biloba Extract; Ginkgo Biloba Linn. Cat No: EXTC-009. |  |
| Ginkgo Biloba Extract | Ginkgo Biloba Extract is a standardized form of extract that is made from the leaves of Ginkgo biloba trees. By standardizing this extract, unwanted levels of naturally occurring impurities such as ginkgolic acids are removed. This ensures that the standardized version of the herb contains the desired concentrations of bioactive components so they can be used for pharmaceutical studies and nutraceutical development. Applications: Uses for ginkgo biloba extract include supporting cognitive function, memory, and increasing blood flow to the brain. it is also commonly used when developing treatments targeting peripheral vascular disease and ocular symptoms like ringing in the ears (tinnitus). Category: Natural extract. Product ID: PIPE-0023. Appearance: Powder. |  |
| Ginkgo Biloba Extract Powder | Ginkgo Biloba Extract has anti-inflammatory, anti-allergic, anti-oxidant, anti-aging properties. It can be used in the preparation of daily essentials such as hand sanitizer. Ginkgo Biloba Extract is widely used in medicine, health products, food additives, functional beverages, cosmetics and other fields. Alternative Names: Ginkgo leaf extract; Ginkgo biloba, ext. Grades: Total flavonol glycosides: NLT 24%. CAS No. 90045-36-6. | |
| Ginkgo Biloba Leaf Powder & P.E. 4:1 | Ginkgo Biloba Leaf Powder & P.E. 4:1. |  CA, FL & NJ |
| Ginkgolic acid | Ginkgolic Acid is a natural compound that inhibits SUMOylation with an IC50 of 3.0 μM in in vitro assay. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ginkgolic acid I. CAS No. 22910-60-7. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0077. | |
| Ginkgolic acid | Ginkgolic acid. Alternative Names: 2-hydroxy-6-(8Z)-8-pentadecenyl-benzoic acid. CAS No. 22910-60-7. Purity: >95.0%. Product ID: FFC-AR-22910607. Molecular formula: C22H34O3. Mole weight: 346.5. IUPAC Name: 2-hydroxy-6-[(Z)-pentadec-8-enyl]benzoic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Ginkgolic Acid | Ginkgolic Acid. CAS No: 22910-60-7 |  Sarchem Laboratories New Jersey NJ |
| Ginkgolic acid 15:1 | Ginkgolic acid 15:1. Group: Biochemicals. CAS No. 22910-60-7. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ginkgolic acid 17:1 | Ginkgolic acid 17:1. Group: Biochemicals. CAS No. 111047-30-4. Pack Sizes: 5mg. US Biological Life Sciences. | 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. | Worldwide |
| Ginkgolic Acid (C13:0) | Ginkgolic Acid (C13:0) (Ginkgoneolic Acid) is an anti-cariogenic agent and a PI3Kδ inhibitor (IC50: 2.49 μM). Ginkgolic Acid (C13:0) exhibits antibacterial and anti-parasitic activities. Ginkgolic Acid (C13:0) can also inhibit mast cell degranulation (IC50: 2.40 μM)[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ginkgolic acid (13:0); Ginkgoneolic Acid; 6-Tridecylsalicylic acid. CAS No. 20261-38-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-N0078. | |
| 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. | 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. | Worldwide |
| Ginkgolic Acid (C15:1) | Ginkgolic Acid is a natural compound with suspected cytotoxic, allergenic, mutagenic and carcinogenic properties. Alternative Names: 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. | |
| 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. | 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. | Worldwide |
| Ginkgolic acid C17:1 | Ginkgolic acid C17:1 is a fatty acid synthase (FAS) inhibitor with an IC50 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. Category: Signaling pathways. CAS No. 111047-30-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-N2116. | |
| Ginkgolic acid C17:1 | Ginkgolic acid C17:1 is a phenol isolated from Ginkgo biloba L. with anticancer effects. Ginkgolic acid C17:1 shows anti-tumor activity by inhibiting the phosphorylation of STAT3 and inducing apoptosis. Alternative Names: Ginkgolic acid 17:1; (Z)-2-(Heptadec-10-en-1-yl)-6-hydroxybenzoic acid; Ginkgolic acid II. Grades: 98%. CAS No. 111047-30-4. Molecular formula: C24H38O3. Mole weight: 374.56. | |
| Ginkgolic acid C17:1 | Ginkgolic acid C17:1. Alternative Names: Ginkgolic Acid II. CAS No. 111047-30-4. Purity: >98.0%. Product ID: FFC-AR-111047304. Molecular formula: C24H38O3. Mole weight: 374.56. IUPAC Name: 2-[(Z)-heptadec-10-enyl]-6-hydroxybenzoic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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. | Worldwide |
| ginkgolic Acids | ginkgolic Acids. CAS No. 5436-2-19. Product ID: ACM1291548. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Ginkgolide A | Ginkgolide A (BN-52020) is an extract from in Ginkgo biloba and a g-aminobutyric acid (GABA) antagonist. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BN-52020. CAS No. 15291-75-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0355. | |
| 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. | Worldwide |
| Ginkgolide A | Ginkgolide A is an extract from in Ginkgo biloba and a g-aminobutyric acid (GABA) antagonist with a Ki of 14.5 μM. 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; 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-dihydroxy-8-methyl-, [1R-(1α,3β,3aS*,4β,6aα,7aα,7bα,8α,10aα,11aS*)]-; [1R-(1α,3β,3aS*,4β,6aα,7aα,7bα,8α,10aα,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; Bilobalide A; BN 52020. Grades: >98%. CAS No. 15291-75-5. Molecular formula: C20H24O9. Mole weight: 408.40. | |
| 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. 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; 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. Grades: >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 | 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 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. 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; 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. Grades: >98%. CAS No. 15291-76-6. Molecular formula: C20H24O11. | |
| 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 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. Alternative Names: 7beta-hydroxyginkgolide a; BN 52024; GinkgolideA, 7-hydroxy-, (7β)-; J Ginkgoli. Grades: >98%. CAS No. 107438-79-9. Molecular formula: C20H24O10. | |
| 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. Alternative Names: 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)-. Grades: 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 | Ginkgolic acid C13:0 exhibited the highest α-glucosidase inhibitory activity. Alternative Names: 6-n-Tridecylsalicylic acid. Grades: >98%. CAS No. 20261-38-5. Molecular formula: C20H32O3. | |
| 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. | |
| Ginseng, Panax quinquefolium, ext. | Ginseng, Panax quinquefolium, ext., commonly known as American ginseng extract, is derived from the root of the Panax quinquefolium plant and is widely used for its adaptogenic, immunomodulatory, and health-promoting properties. It enhances immune function by boosting the production of IL-2 and IFN-gamma in immune cells, improves cognitive function by reducing fatigue and alleviating stress, supports cardiovascular health by regulating blood pressure and improving heart function, regulates blood sugar levels to help manage diabetes, and offers antioxidant and anti-inflammatory effects that protect cells from oxidative damage. In traditional medicine, it is used to tonify the spleen and lungs, nourish yin, clear heat, and alleviate respiratory conditions like chronic cough and asthma. It is also used in cosmetics for its skin-benefiting properties, such as reducing wrinkles, improving skin elasticity, and brightening the complexion. Alternative Names: Ginseng Extract; Panax quinquefolium, ext.; Panax quinquefolium extract; American ginseng extract; Ginseng, Panax quinquefolium extract. Grades: 5%-80%. CAS No. 90045-38-8. | |
| 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 is an intestinal microbiota metabolite of ginsenoside Rb1, which possesses anti-proliferative and anti-inflammatory activities. Alternative Names: Ginsenoside K. Grades: >98%. CAS No. 39262-14-1. Molecular formula: C36H62O8. Mole weight: 622.87. | |
| 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 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, 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. 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, 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. Alternative Names: (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. Grades: >98%. CAS No. 53963-43-2. Molecular formula: C36H62O9. Mole weight: 638.87. | |
| 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 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 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. Alternative Names: (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. Grades: >98%. CAS No. 62025-49-4. Molecular formula: C42H72O13. Mole weight: 785.01. | |
| 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 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. Alternative Names: (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 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 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. Alternative Names: Ginsenoside Rg6; (20E)-Ginsenoside F4. Grades: >98%. CAS No. 181225-33-2. Molecular formula: C42H70O12. Mole weight: 767. | |
| Ginsenoside F5 | Ginsenoside F5 is extracted from the root of Panax ginseng C. A. Mey. Alternative Names: 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. | |
| 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 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. Alternative Names: 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. | |
| 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. Alternative Names: 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. | |
| 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. Alternative Names: 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. | |
| 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. Alternative Names: 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. Grades: ≥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. | |
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