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| Product | Description | |
|---|---|---|
| Gingerenone A | Gingerenone A is a natural product found in Zingiber officinale. Gingerenone A is a dual inhibitor of JAK2 and S6K1 pathways, it selectively kills cancer cells while exhibiting minimal toxicity toward normal cells. Synonyms: 1,7-bis(4-hydroxy-3-methoxyphenyl)hept-4-en-3-one; (4E)-1,7-Bis(4-hydroxy-3-methoxyphenyl)-4-hepten-3-one. Grade: 98%. CAS No. 128700-97-0. Molecular formula: C21H24O5. Mole weight: 356.41. |  |
| Ginger Extract | Ginger Extract. Applications: Ginger extract can be used in functional food, drinks, health care products and pharmaceuticals. Group: Others. Purity: 5:1 10:1 20:1 or as customers requirements. Appearance: Yellowish-brown Powder. Source: Ginger (Zingiber officinale) is a flowering plant, in the family Zingiberaceae whose rhizome, ginger root or simply ginger, is widely used as a spice or a folk medicine. Ginger Extract; Zingiber officinale Rosc. Cat No: EXTC-183. |  |
| Ginger oil | Ginger oil. Alternative Names: Ginger terpeneless. CAS No. 8007-8-7. Purity: 0.98. Product ID: CI-EO-0043. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Ginger Oil Chinese | Ginger Oil Chinese. CAS No. 8007-08-7. FEMA No. 2522. Kosher: Y. VIGON Item # 504286. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Ginger Oil - CO2 | Ginger CO2 is extracted in such a way that it also contains gingerols and shogaol, compounds that contribute to the sharp, pungent smell and taste of fresh ginger. The aroma of Ginger CO2 extract is spicy and warm, very dense and more complex than that of distilled Ginger - it smells just like the freshly harvested root. Ginger CO2 is a pale yellow to greenish yellow oil and is quite potent, so it is best to use it in low percentages. Traditionally used for its warming action, Ginger Root CO2 Total Extract aids digestion, stimulates blood flow and helps relieve a queasy stomach and menstrual discomfort. When added to a carrier oil or lotion, it helps joint and muscle aches associated with the wear and tear of normal aging. Uses: Aromatherapy, Flavour, Cosmetic and Care. Group: Plant Extracts. INCI Names: Zingiber Officinale (Ginger) Root Oil. Grades: FOOD GRADE. CAS No. 84696-15-1; 8007-08-7. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: FG-003. Olfactive Profile: Warm, spicy, pungent, woody, earthy, aromatic, sweet, citrus. EC No: 283-634-2. FEMA No: 2522. Origin: Indonesia. |  New Jersey |
| Ginger Oil Cochin | Ginger Oil Cochin. CAS No. 8007-08-7. FEMA No. 2522. VIGON Item # 509114. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Cosmetics, Aromatherapy, Essetial Oils. | America & Internationally |
| Gingerol | Gingerol. Grades: Various grades and purity. CAS No. 23513-14-6. Pack Sizes: Various packaging available. Categories: Supplement. |  US, Austria, Lithuania |
| Ginger Oleoresin African | Ginger Oleoresin African. CAS No. 84696-15-1. FEMA No. 2521. Kosher: Y. VIGON Item # 501251. Categories: Speciality Ingrdients Suppliers, Flavors. | America & Internationally |
| Ginger Powder | Ginger powder is made from fresh ginger, the underground stem, or rhizome, of the plant zingiber officinale. Ginger powder is be valued around the world as an important cooking spice and is believed to help the common cold, flu-like symptoms, headaches, and even painful menstual periods. Ginger powder also possesses a special efficacy of relieving seasick and carsick. Group: Others. Ginger Powder; Zingiber Officinale Roscoe. Cat No: EXTC-108. | |
| Ginger Root Powder | Ginger Root Powder. |  CA, FL & NJ |
| Ginger SFE | Ginger SFE. CAS No. 8007-08-7. FEMA No. 2522. Kosher: Y. VIGON Item # 504601. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| gingipain K | Activity is stimulated by glycine. Known from the bacterium Porphyromonas gingivalis and contributes to the pathogenicity of the organism. In peptidase family C25. Group: Enzymes. Synonyms: Lys-gingipain; PrtP proteinase. Enzyme Commission Number: EC 3.4.22.47. CAS No. 159745-69-4. 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-4222; gingipain K; EC 3.4.22.47; 159745-69-4; Lys-gingipain; PrtP proteinase. Cat No: EXWM-4222. | |
| gingipain R | A secreted endopeptidase from the bacterium Porphyromonas gingivalis. Strongly activated by glycine, and stabilized by Ca2+. Precursor molecule contains a hemagglutinin domain. Misleadingly described in some literature as "trypsin-like", being a cysteine peptidase, type example of family C25. Group: Enzymes. Synonyms: Arg-gingipain; gingipain-1; argingipain; Arg-gingivain-55 proteinase; Arg-gingivain-70 proteinase; Arg-gingivain-75 proteinase; arginine-specific cysteine protease; arginine-specific gingipain; arginine-specific gingivain; RGP-1; RGP. Enzyme Commission Number: EC 3.4.22.37. CAS No. 159745-71-8. 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-4212; gingipain R; EC 3.4.22.37; 159745-71-8; Arg-gingipain; gingipain-1; argingipain; Arg-gingivain-55 proteinase; Arg-gingivain-70 proteinase; Arg-gingivain-75 proteinase; arginine-specific cysteine protease; arginine-specific gingipain; arginine-specific gingivain; RGP-1; RGP. Cat No: EXWM-4212. | |
| Gingko Biloba Leaf Extract 24% Flavone Glycoside / 6% Terpene Lactones | Gingko Biloba Leaf Extract 24% Flavone Glycoside / 6% Terpene Lactones. | CA, FL & NJ |
| Ginisortamab | Ginisortamab (UCB6114) is a fully human IgG4P anti Gremlin-1 monoclonal antibody, with mean IC50 values of 8.2 nM and 9 nM against human and mouse gremlin-1, respectivly. Ginisortamab inhibits gremlin-1 antagonism of BMP signaling pathways. Ginisortamab has the potential for the research of gastrointestinal (GI) tumors[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: UCB6114. CAS No. 2390147-17-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99643. |  |
| 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 Inhibitor. Uses: Scientific use. Product Category: T4S2126. CAS No. 481-46-9. |  |
| 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, 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 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 | 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 Leaf Powder & P.E. 4:1 | Ginkgo Biloba Leaf Powder & P.E. 4:1. | CA, FL & NJ |
| 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 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. 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 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. 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 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. 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 is an extract from in Ginkgo biloba and a g-aminobutyric acid (GABA) antagonist with a Ki of 14.5 μM. Synonyms: (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. Grade: >98%. CAS No. 15291-75-5. Molecular formula: C20H24O9. Mole weight: 408.40. | |
| 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 (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 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 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 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 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 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. 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. 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, 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, 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. | |
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