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| Product | Description | |
|---|---|---|
| INF7 | INF7 is a derivative of the N-terminal domain of the HA2 protein and is sensitive to pH. INF7 disrupts the stability of endosomal membranes through a mechanism independent of membrane fusion. INF7 can be used to enhance the endosome escape of complex or liposome-encapsulated proteins. Co-encapsulation of INF7 and molecular imaging probes in liposomes can enhance intracellular signaling and probe retention[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 185462-59-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P10152. |  |
| IN-F 7321 | IN-F 7321. Group: Biochemicals. Alternative Names: 1,1-Bis(4-fluorophenyl)-1-methyl-silanol. Grades: Highly Purified. CAS No. 156162-13-9. Pack Sizes: 50mg. Molecular Formula: C13H12F2OSi, Molecular Weight: 250.32. US Biological Life Sciences. |  Worldwide |
| infectious pancreatic necrosis birnavirus Vp4 peptidase | Infectious pancreatic necrosis virus (IPNV) is a birnavirus that causes an acute, contagious disease in young salmonid fish. As with most viruses that infect eukaryotic cells, the proteolytic processing of viral precursor proteins is a crucial step in the life cycle of this virus. pVP2 is converted into VP2 by cleavage near the carboxy end of pVP2. This cleavage is most likely due to host-cell proteases rather than VP4. Differs from most serine peptidases in not having the catalytic triad Ser-His-Asp. Belongs in peptidase family S50. Group: Enzymes. Synonyms: infectious pancreatic necrosis virus protease; IPNV Vp4 protease; IPNV Vp4 peptidase; NS protease; NS-associated protease; Vp4 protease. Enzyme Commission Number: EC 3.4.21.115. 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-4110; infectious pancreatic necrosis birnavirus Vp4 peptidase; EC 3.4.21.115; infectious pancreatic necrosis virus protease; IPNV Vp4 protease; IPNV Vp4 peptidase; NS protease; NS-associated protease; Vp4 protease. Cat No: EXWM-4110. |  |
| Infigratinib | Infigratinib (BGJ-398; NVP-BGJ398) is a potent inhibitor of the FGFR family with IC50s of 0.9 nM, 1.4 nM, 1 nM, and 60 nM for FGFR1, FGFR2, FGFR3, and FGFR4, respectively. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BGJ-398; NVP-BGJ398. CAS No. 872511-34-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-13311. | |
| Infigratinib-Boc | Infigratinib-Boc is a derivative of Infigratinib containing a Boc (t-Butyloxy carbonyl) group. Infigratinib is an ATP-competitive pan-FGFR inhibitor[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2504949-83-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-160124. | |
| INFINITY CHOLESTEROL, CUSTOM PACK | INFINITY CHOLESTEROL, CUSTOM PACK. Product ID: ACMA00005195. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| INFINITY CHOLESTEROL REAGENT | INFINITY CHOLESTEROL REAGENT. Product ID: ACMA00005138. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Inflachromene | Inflachromene, a microglial inhibitor, binds to HMGB1 and HMGB2 and exerts anti-inflammatory effects. Inflachromene effectively downregulates proinflammatory functions of HMGB and reduces neuronal damage. Inflachromene can be used for the research of neuroinflammatory disorders[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 908568-01-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113772. | |
| Infliximab | Infliximab Inhibitor. Uses: Scientific use. Product Category: T9921. CAS No. 170277-31-3. |  |
| Infliximab | Infliximab (Avakine) is a chimeric monoclonal IgG1 antibody that specifically binds to TNF-α. Infliximab prevents the interaction of TNF-α with TNF-α receptor (TNFR1 and TNFR2). Infliximab has the potential for autoimmune, chronic inflammatory diseases and diabetic neuropathy research[1][2]. The component ratio of this product is Active ingredient : Excipients = 9 : 47. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Avakine; CT-P13; SB2; TA-650. CAS No. 170277-31-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P9970. | |
| Infliximab (anti-TNF-alpha) | Infliximab (anti-TNF-alpha) is a purified, recombinant DNA-derived chimeric human-mouse IgG monoclonal antibody that consists of mouse heavy and light chain variable regions combined with human heavy and light chain constant regions. Infliximab neutralizes the biological activity of TNF-α by binding with high affinity to the soluble and transmembrane forms of TNF-α, and inhibits or prevents the effective binding of TNF-α with its receptors. MW=144.2 kDa. Group: Antibodies. CAS No. 170277-31-3. Pack Sizes: 5mg. Product ID: A2019. Storage Conditions: Store the undiluted solution at 4°C in the dark to avoid freeze-thaw cycles. |  United States; Europe |
| Influenza A NP (366-374) Strain A/NT/60/68 | Influenza A NP (366-374) Strain A/NT/60/68 is an H2-Db-restricted epitope from the Influenza A/NT/60/68 nucleoprotein. Synonyms: H-Ala-Ser-Asn-Glu-Asn-Met-Asp-Ala-Met-OH; Ala-Ser-Asn-Glu-Asn-Met-Asp-Ala-Met. Molecular formula: C36H59N11O17S2. Mole weight: 982.08. |  |
| Influenza A NP (366-374) Strain A/PR/8/35 | Influenza A NP (366-374) Strain A/PR/8/35 is an H2-Db-restricted epitope from the nucleoprotein of Influenza A/PR/8/35. Synonyms: L-Methionine, L-alanyl-L-seryl-L-asparaginyl-L-α-glutamyl-L-asparaginyl-L-methionyl-L-α-glutamyl-L-threonyl-; Ala-Ser-Asn-Glu-Asn-Met-Glu-Thr-Met. Grade: ≥95%. CAS No. 132326-73-9. Molecular formula: C38H63N11O18S2. Mole weight: 1026.10. | |
| Influenza A NP(366-374) Strain A/PR/8/35 | Influenza A NP(366-374) Strain A/PR/8/35 is an H2-Db-restricted epitope from Influenza A/PR/8/35 nucleoprotein[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 132326-73-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1788. | |
| Influenza HA 126-138 | Influenza HA 126-138 is an influenza virus hemagglutinin (HA) peptide composed of 126-138 amino acids that induces apoptosis of T cells in thymus and peripheral blood. Synonyms: L-Glutamic acid, L-histidyl-L-asparaginyl-L-threonyl-L-asparaginylglycyl-L-valyl-L-threonyl-L-alanyl-L-alanyl-L-seryl-L-seryl-L-histidyl-; His-Asn-Thr-Asn-Gly-Val-Thr-Ala-Ala-Ser-Ser-His-Glu. Grade: ≥95%. CAS No. 207349-63-1. Molecular formula: C52H81N19O22. Mole weight: 1324.31. | |
| Influenza HA 126-138 acetate | Influenza HA 126-138 acetate is an influenza virus hemagglutinin (HA) peptide composed of 126-138 amino acids that induces apoptosis of T cells in the thymus and peripheral blood. Synonyms: H-His-Asn-Thr-Asn-Gly-Val-Thr-Ala-Ala-Ser-Ser-His-Glu-OH.CH3CO2H; L-histidyl-L-asparagyl-L-threonyl-L-asparagyl-glycyl-L-valyl-L-threonyl-L-alanyl-L-alanyl-L-seryl-L-seryl-L-histidyl-L-glutamic acid acetic acid. Grade: ≥95%. Molecular formula: C52H81N19O22. Mole weight: 1324.33. | |
| Influenza HA 307-319 | Influenza HA 307-319 is a 307-319 amino acid fragment of Influenza HA, which is a glycoprotein found on the surface of influenza viruses. Synonyms: Pro-Lys-Tyr-Val-Lys-Gln-Asn-Thr-Leu-Lys-Leu-Ala-Thr; L-prolyl-L-lysyl-L-tyrosyl-L-valyl-L-lysyl-L-glutaminyl-L-asparagyl-L-threonyl-L-leucyl-L-lysyl-L-leucyl-L-alanyl-L-threonine. Grade: ≥95%. CAS No. 528526-85-4. Molecular formula: C69H118N18O19. Mole weight: 1503.78. | |
| Influenza HA 518-526 | Influenza HA 518-526 is an H-2Kd-restricted epitope of the influenza virus hemagglutinin. Synonyms: H-Ile-Tyr-Ser-Thr-Val-Ala-Ser-Ser-Leu-OH; L-isoleucyl-L-tyrosyl-L-seryl-L-threonyl-L-valyl-L-alanyl-L-seryl-L-seryl-L-leucine. Grade: ≥95%. CAS No. 186302-15-8. Molecular formula: C42H69N9O15. Mole weight: 940.05. | |
| Influenza Hemagglutinin (HA) Peptide | Influenza Hemagglutinin (HA) Peptide. Uses: For analytical and research use. CAS No. 92000-76-5. Mole weight: 1102.15. Catalog: AP92000765. |  |
| Influenza NP 147-155 | Influenza NP 147-155 is a Kd-restricted epitope from influenza nucleoprotein. Synonyms: Thr-Tyr-Gln-Arg-Thr-Arg-Ala-Leu-Val; L-threonyl-L-tyrosyl-L-glutaminyl-L-arginyl-L-threonyl-L-arginyl-L-alanyl-L-leucyl-L-valine. Grade: ≥95%. CAS No. 132326-72-8. Molecular formula: C48H82N16O14. Mole weight: 1107.26. | |
| Influenza Virus Nucleoprotein (311-325) | Influenza Virus Nucleoprotein (311-325) is a peptide that corresponds to aa 311-325 of Influenza A virus nucleoprotein. NP is a critical component of the viral ribonucleoproteins (vRNP) complex, and the recognized functions of NP include, but are not limited to, organization of RNA packing, nuclear trafficking, and vRNA transcription and replication. Synonyms: Influenza Virus NP (311-325); H-Gln-Val-Tyr-Ser-Leu-Ile-Arg-Pro-Asn-Glu-Asn-Pro-Ala-His-Lys-OH. Molecular formula: C78H124N24O23. Mole weight: 1766.1. | |
| Infusion bottle with aluminum-plastic composite cover | Infusion bottle aluminum-plastic combination cover is mainly made of aluminum alloy plate stamping, it has a variety of classification, according to the number of flowering points is different, divided into two flowering, three flowering and so on. Product ID: PM-067. Category: Aluminum caps. Product Keywords: Plastic Packaging; Infusion bottle with aluminum-plastic composite cover; PM-067; Aluminum caps;. Administration route: According to the different flowering mode, it can be divided into internal flowering and external flowering. |  |
| Ingavirin-[d6] | Ingavirin-[d6] is the labelled analogue of Ingavirin. Ingavirin is a drug with potential therapeutic effect on Influenza and other acute viral respiratory infections. Synonyms: Ingavirin-D6. Grade: 95% by HPLC; 95% atom D. Molecular formula: C10H9D6N3O3. Mole weight: 231.28. | |
| Ingenol | Loss of Drying: Group: Biochemicals. Grades: Plant Grade. CAS No. 30220-46-3. Pack Sizes: 20mg. US Biological Life Sciences. | Worldwide |
| Ingenol | Ingenol. Group: Biochemicals. CAS No. 30220-46-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ingenol 3,20-dibenzoate | Ingenol 3,20-dibenzoate is a potent protein kinase C (PKC) isoform-selective agonist. Ingenol 3,20-dibenzoate induces selective translocation of nPKC-delta, -epsilon, and -theta and PKC-mu from the cytosolic fraction to the particulate fraction and induces morphologically typical apoptosis through de novo synthesis of macromolecules. Ingenol 3,20-dibenzoate increases the IFN-γ production and degranulation by NK cells, especially when NK cells are stimulated by NSCLC cells[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 59086-90-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-137295. | |
| Ingenol-3,4:5,20-diacetonide | Ingenol-3,4:5,20-diacetonide. Group: Biochemicals. Grades: Plant Grade. CAS No. 77573-44-5. Pack Sizes: 20mg. Molecular Formula: C26H36O5, Molecular Weight: 428.56. US Biological Life Sciences. | Worldwide |
| Ingenol-3-angelate | Ingenol 3-Angelate is a diterpenoid ester isolated from Euphorbia peplus that induces rapid cell death with keratinocytes and some cancer cell lines. Ingenol 3-Angelate is a protein kinase C activator that displays potent antileukemic activity. Ingenol 3-Angelate (ingenol mebutate) is used for treatment of actinic keratosis.Source:Semi-synthetic, the starting material ingenol was isolated from Euphorbia latyris. Group: Biochemicals. Grades: Highly Purified. CAS No. 75567-37-2. Pack Sizes: 1mg, 5mg. Molecular Formula: C25H34O6. US Biological Life Sciences. | Worldwide |
| Ingenol 3-Angelate | Ingenol 3-Angelate. Group: Biochemicals. Alternative Names: (2Z)-2-Methyl-2-butenoic Acid (1aR, 2S, 5R, 5aS, 6S, 8aS, 9R, 10aR) -1a, 2, 5, 5a, 6, 9, 10, 10a-Octahydro-5, 5a-dihydroxy-4- (hydroxymethyl) -1, 1, 7, 9-tetramethyl-11-oxo-1H-2, 8a-methanocyclopenta [a]cyclopropa [e]cyclodecen-6-yl Ester; 3-Angeloylingenol; 3-Ingenyl angelate; Euphorbia factor An1; Euphorbia factor H1; Ingenol mebutate; PEP 005; Picato. Grades: Highly Purified. CAS No. 75567-37-2. Pack Sizes: 2.5mg. Molecular Formula: C25H34O6, Molecular Weight: 430.53. US Biological Life Sciences. | Worldwide |
| Ingenol-3-mebutate | Ingenol-3-mebutate is a substance found in the sap of the plant Euphorbia peplus and an inducer of cell death. It is effective for field treatment of actinic keratoses, significantly reduced head and non-head actinic keratosis lesions. Synonyms: PEP005; PEP-005; PEP 005; ingenol-3-angelate; Ingenol mebutate. Grade: >98%. CAS No. 75567-37-2. Molecular formula: C25H34O6. Mole weight: 430.53. | |
| Ingenol-5,20-acetonide | Intermediate and starting material for the synthesis and preparation of ingenol 3-ester derivatives. For use in chemical synthesis see references. Has improved shelf life compared to ingenol. Source:Semi-synthetic. Group: Biochemicals. Grades: Highly Purified. CAS No. 77573-43-4. Pack Sizes: 1mg, 5mg. Molecular Formula: C23H32O5. US Biological Life Sciences. | Worldwide |
| Ingenol Mebutate | Ingenol Mebutate is an active ingredient in Euphorbia peplus, acts as a potent PKC modulator, with Kis of 0.3, 0.105, 0.162, 0.376, and 0.171 nM for PKC-α, PKC-β, PKC-γ, PKC-δ, and PKC-ε, respectively, and has antiinflammatory and antitumor activity. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ingenol 3-angelate; PEP005. CAS No. 75567-37-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0719. | |
| INH1 | INH1. Group: Biochemicals. Grades: Purified. CAS No. 313553-47-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| INH154 | INH154 is a highly potent inhibitor for Nek2 and Hec1 binding (INH), with IC50s of 200 nM and 120 nM for INH in Hela and MB468 cells. Uses: Scientific research. Category: Signaling pathways. CAS No. 1587705-63-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-117154. | |
| Inhibitor Library | A unique collection of 5700 inhibitors for research in cell signaling, high throughput screening (HTS) and high content screening (HCS) for new drugs; - Bioactivity and safety confirmed by pre-clinical research and clinical trials, and some of them are approved by FDA; - Covers various major targets including MAPK, PI3K, JAK, HDAC, VEGFR, CDK, etc. ; - Detailed compound information with structure, target, activity, IC50 value, and biological activity description; - Structurally diverse, medicinally active, and cell permeable; - NMR and HPLC validated to ensure high purity and quality. Uses: Scientific use. Product Category: L2000. Categories: Inhibitor Libraries. | |
| Inhoffen lythgoe diol | Inhoffen lythgoe diol. Group: Biochemicals. Alternative Names: (b-S,1R,3aR,4S,7aR)-Octahydro-4-hydroxy-b,7a-dimethyl-1H-indene-1-ethanol; (1R,3aR,4S,7aR)-1-((S)-1-Hydroxypropan-2-yl)-7a-methyloctahydro-1H-inden-4-ol. Grades: Highly Purified. CAS No. 64190-52-9. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C13H24O2. US Biological Life Sciences. | Worldwide |
| Inhoffen Lythgoe Diol. | A key intermediate for the preparation of Vitamin D metabolites and analogs. Group: Biochemicals. Alternative Names: ( βS,1R,3aR,4S,7aR)--Octahydro-4-hydroxy- β,7a-dimethyl- 1H-indene-1-ethanol. Grades: Highly Purified. CAS No. 64190-52-9. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Inhoffen lythgoe diol monotosylate | Inhoffen lythgoe diol monotosylate. Group: Biochemicals. Alternative Names: (b-S,1R,3aR,4S,7aR)-Octahydro-4-hydroxy-b,7a-dimethyl-1H-indene-1-ethanol 1- (4-Methyl Benzene sulfonate) . Grades: Highly Purified. CAS No. 66774-80-9. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C20H30O4S. US Biological Life Sciences. | Worldwide |
| INI-43 | INI-43 is an inhibitor of Kpnβ1, interfering with the nuclear localization of Kpnβ1 and known Kpnβ1 cargo proteins, NFAT, NFκB, AP-1, and NFY. INI-43 can inhibit the proliferation of cancer cells, cause G2-M cell cycle arrest in cancer cells, and induce the intrinsic apoptosis pathway[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 881046-01-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121607. | |
| Iniparib | Iniparib is an irreversible PARP1 inhibitor. Studies show that potential therapeutic agent for the treatment of cancer, including triple-negative breast cancer. Group: Biochemicals. Alternative Names: 4-Iodo-3-nitrobenzamide; BSI 201. Grades: Highly Purified. CAS No. 160003-66-7. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Iniparib | Iniparib (BSI-201) is an irreversible inhibitor of PARP1, used in the research of triple negative breast cancer. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BSI-201; NSC-746045; IND-71677. CAS No. 160003-66-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-12015. | |
| initiation-specific α-1,6-mannosyltransferase | Requires Mn2+. In Saccharomyces cerevisiae, this enzyme catalyses an essential step in the outer chain elongation of N-linked oligosaccharides. Man8GlcNAc and Man9GlcNAc are equally good substrates. Group: Enzymes. Synonyms: α-1,6-mannosyltransferase; GDP-mannose:oligosaccharide 1,6-α-D-mannosyltransferase; GDP-mannose:glycolipid 1,6-α-D-mannosyltransferase; glycolipid 6-α-mannosyltransferase; GDP-mannose:oligosaccharide 1,6-α-D-mannosyltransferase. Enzyme Commission Number: EC 2.4.1.232. CAS No. 346003-17-6. 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-2462; initiation-specific α-1,6-mannosyltransferase; EC 2.4.1.232; 346003-17-6; α-1,6-mannosyltransferase; GDP-mannose:oligosaccharide 1,6-α-D-mannosyltransferase; GDP-mannose:glycolipid 1,6-α-D-mannosyltransferase; glycolipid 6-α-mannosyltransferase; GDP-mannose:oligosaccharide 1,6-α-D-mannosyltransferase. Cat No: EXWM-2462. | |
| initiation-specific α-1,6-mannosyltransferase | Requires Mn2+. In Saccharomyces cerevisiae, this enzyme catalyses an essential step in the outer chain elongation of N-linked oligosaccharides. Man8GlcNAc and Man9GlcNAc are equally good substrates. | |
| Injection Bottles | Injection Bottles. Product ID: PM-010. Product Keywords: Packaging Materials; Glass Packaging; PM-010; Injection Bottles. Color: Clear/Amber. | |
| Injection Vials | Injection Vials. Product ID: PM-029. Product Keywords: Packaging Materials; Glass Packaging; PM-029; Injection Vials. | |
| Inner centromere protein (48-56) | A fragment of Inner centromere protein. Inner centromere protein (INCENP) is a component of the chromosomal passenger complex (CPC), which is an important regulator of mitosis. It can be used in Ovarian carcinoma research. | |
| INNO-206 | INNO-206 (Aldoxorubicin) is the 6-maleimidocaproyl hydrazone derivative prodrug of the anthracycline antibiotic doxorubicin (DOXO-EMCH) with antineoplastic activity. Uses: Adcs cytotoxin-linker. Synonyms: Doxorubicin-hydrazone-caproyl-maleimide; Aldoxorubicin; 2,5-Dihydro-2,5-dioxo-1H-pyrrole-1-hexanoic acid (2E)-2-[1-[(2S,4S)-4-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-1,2,3,4,6,11-hexahydro-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-2-naphthacenyl]-2-hydroxyethylidene]hydrazide; 1H-Pyrrole-1-hexanoic acid, 2,5-dihydro-2,5-dioxo-, (2E)-2-[1-[(2S,4S)-4-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-1,2,3,4,6,11-hexahydro-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-2-naphthacenyl]-2-hydroxyethylidene]hydrazide; INNO 206; INNO206. Grade: >98%. CAS No. 1361644-26-9. Molecular formula: C37H42N4O13. Mole weight: 750.75. | |
| INNO-220 | INNO-220 is an orally active, CRBN-dependent molecular glue degrader targeting CK1α. INNO-220 induces cell cycle arrest at G0/G1 phase and triggers apoptosis by degrading CK1α. INNO-220 disrupts the assembly and function of the CARD11/BCL10/MALT1 complex, thereby inhibiting NF-κB signaling in stimulated T cells and lymphoma cells that harbor an activating mutation in CARD11. INNO-220 provides a new direction for lymphoma research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3032576-92-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-174371. | |
| Inobrodib | Inobrodib (CCS1477) is an orally active, potent, and selective inhibitor of the p300/CBP bromodomain. Inobrodib binds to p300 and CBP with Kd values of 1.3 and 1.7 nM, respectively, and with 170/130-fold selectivity compared with BRD4 with a Kd of 222 nM. CCS1477 inhibits cell proliferation in prostate cancer cell lines and decreases androgen receptor (AR)- and C-MYC-regulated gene expression[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CCS1477. CAS No. 2222941-37-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111784. | |
| Inobrodib (CCS-1477) | Inobrodib (CCS1477; CBP-IN-1; CBP/p300-IN-4) is a potent and selective inhibitor of p300/CBP bromodomain. CCS1477 works by inhibiting the expression and function of the androgen receptor (AR), as well as inhibiting c-Myc. Group: Inhibitors. Alternative Names: CBP-IN-1, CBP/p300-IN-4. CAS No. 2222941-37-7. Pack Sizes: 5mg. Product ID: S9667. Formula: C30H32F2N4O3. Smiles: CC1=C(C(=NO1)C)C2=CC3=C(C=C2)N(C(=N3)C4CCCC(=O)N4C5=CC(=C(C=C5)F)F)C6CCC(CC6)OC. Storage Conditions: 3 years -20°C powder. | United States; Europe |
| Inolitazone dihydrochloride | Inolitazone dihydrochloride (Efatutazone dihydrochloride) is a novel high-affinity PPARγ agonist that is dependent upon PPARγ for its biological activity with IC50 of 0.8 nM for growth inhibition. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Efatutazone dihydrochloride; CS-7017 dihydrochloride; RS5444 dihydrochloride. CAS No. 223132-38-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14792B. | |
| Inonotus Obliquus Extract | Inonotus Obliquus Extract. Applications: It ues for treat diabetes. anticancer.prevent and cure aids,antiaging.inhibit infectious virus.prevent high blood pressure.relieve and prevent allergic cortex.have obvious curative effect on hepatitis, gastritis, duodenal ulcer, nephritis. Group: Others. Synonyms: Inonotus Obliquus Extract; Fuscoporia obliqua. Purity: 20%-30% Polysaccharides. Appearance: Brown fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Fruit. Species: Fuscoporia obliqua. Inonotus Obliquus Extract; Fuscoporia obliqua; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-171. | |
| inorganic diphosphatase | Specificity varies with the source and with the activating metal ion. The enzyme from some sources may be identical with EC 3.1.3.1 (alkaline phosphatase) or EC 3.1.3.9 (glucose-6-phosphatase). A form of this enzyme with a molecular mass of about 90 kDa is found in tonoplasts of plants and fungi, where it imports protons from the cytosol into the vacuolar lumen. Group: Enzymes. Enzyme Commission Number: EC 3.6.1.1. CAS No. 9024-82-2. Inorganic pyrophosphatase. 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-4593; inorganic diphosphatase; EC 3.6.1.1; 9024-82-2. Cat No: EXWM-4593. | |
| Inorganic Diphosphatase (Crude Enzyme) | This enzyme belongs to the family of hydrolases, specifically those acting on acid anhydrides in phosphorus-containing anhydrides. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Molecular biology; synthesis; drug development. Group: Enzymes. Enzyme Commission Number: EC 3.6.1.1. CAS No. 9024-82-2. Inorganic pyrophosphatase. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. Inorganic pyrophosphatase. Pack: 100ml. Cat No: NATE-1843. | |
| Inorganic perovskite quantum dots CsPbX3 | Inorganic perovskite quantum dots CsPbX3. |  |
| Inorganic Pyrophosphatase from Escherichia coli, Recombinant | Pyrophosphatase (or inorganic pyrophosphatase) is an enzyme (EC 3.6.1.1) that catalyzes the conversion of one molecule of pyrophosphate to two phosphate ions. This is a highly exergonic reaction, and therefore can be coupled to unfavorable biochemical transformations in order to drive these transformations to completion. The functionality of this enzyme plays a critical role in lipid metabolism (including lipid synthesis and degradation), calcium absorption and bone formation, and DNA synthesis,as well as other biochemical transformations. Applications: Inorganic pyrophosphatase (ppase) is a ubiquitous enzyme catalyzing the reaction ppi + h2o ? 2pi. it plays an important role in protein, rna, and dna synthesis. Group: Enzymes. Synonyms: Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. Enzyme Commission Number: EC 3.6.1.1. CAS No. 9024-82-2. Purity: > 90%. Inorganic pyrophosphatase. Activity: > 800 units/mg protein. Storage: -20°C. Form: Lyophilized powder in Tris-buffered salts containing protease inhibitors. Source: E. coli. Species: Escherichia coli. Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. Cat No: NATE-0355. | |
| Inorganic Pyrophosphatase from Saccharomyces cerevisiae, Recombinant | Pyrophosphatase (or inorganic pyrophosphatase) is an enzyme (EC 3.6.1.1) that catalyzes the conversion of one molecule of pyrophosphate to two phosphate ions. This is a highly exergonic reaction, and therefore can be coupled to unfavorable biochemical transformations in order to drive these transformations to completion. The functionality of this enzyme plays a critical role in lipid metabolism (including lipid synthesis and degradation), calcium absorption and bone formation, and DNA synthesis,as well as other biochemical transformations. Inorganic pyrophosphatase (ppase) catalyzes the hydrolysis of inorganic pyrophosphate to form orthophosphate. a variety.actions that can be pulled far in the synthesis direction by the action of inorganic pyrophosphatase. Applications: Enhancing yields of rna in transcription reactions. Group: Enzymes. Synonyms: Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. CAS No. 9024-82-2. Inorganic pyrophosphatase. Mole weight: 71 kDa. Storage: at -20°C. Form: 20 mM Tris-HCl (pH 8.0), 100 mM KCl, 0.1 mM EDTA, 1 mM dithiothreitol and 50% glycerol. Source: E. coli. Species: Saccharomyces cerevisiae. Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. Cat No: NATE-1281. | |
| Inorganic Silica Core/Shell Nanoparticles | Inorganic Silica Core/Shell Nanoparticles. Purity: 99.9%. | |
| Inosamycin A | Inosamycin A is a broad-spectrum antimicrobial antibiotic originally isolated from Str. hygroscopicus No. J296-21. Its antibacterial activity was comparable to that of neomycin, and about twice that of ribomycin. Synonyms: Bu 2659A; 6-Amino-2-{[3-O-(2,6-diamino-2,6-dideoxyhexopyranosyl)pentofuranosyl]oxy}-3,4-dihydroxycyclohexyl 2,6-diamino-2,6-dideoxyhexopyranoside. CAS No. 91421-97-5. Molecular formula: C23H45N5O14. Mole weight: 615.63. | |
| Inosamycin B | Inosamycin B is a broad-spectrum antimicrobial antibiotic originally isolated from Str. hygroscopicus No. J296-21. Its antibacterial activity is about half that of Inosamycin A. Synonyms: Bu 2659B; BMY-28163; 4-O-(2,6-Diamino-2,6-dideoxy-α-D-glucopyranosyl)-5-O-[3-O-(2,6-diamino-2,6-dideoxy-α-D-glucopyranosyl)-β-D-ribofuranosyl]-3-amino-2,3-dideoxy-D-myo-inositol. CAS No. 91465-52-0. Molecular formula: C23H45N5O14. Mole weight: 615.63. | |
| iNOS Antibody [D1F5] | iNOS,iNOS/NOS Type II. Group: Antibodies. Alternative Names: iNOS,iNOS/NOS Type II. Pack Sizes: 20uL. Product ID: F0177. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. | United States; Europe |
| iNOS Antibody [G10L10] | iNOS Antibody [G10L10]. Group: Antibodies. Alternative Names: NOS2A; NOS2; Hepatocyte NOS; Inducible NO synthase; NOS type II; Peptidyl-cysteine S-nitrosylase NOS2; HEP-NOS; Inducible NOS; iNOS. CAS No. Pack Sizes: 20uL. Product ID: F4863. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. | United States; Europe |
| inosinate nucleosidase | This enzyme belongs to the family of hydrolases, specifically those glycosylases that hydrolyse N-glycosyl compounds. The systematic name of this enzyme class is 5'-inosinate phosphoribohydrolase. This enzyme participates in purine metabolism. Group: Enzymes. Synonyms: 5'-inosinate phosphoribohydrolase. Enzyme Commission Number: EC 3.2.2.12. CAS No. 37288-61-2. 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-3966; inosinate nucleosidase; EC 3.2.2.12; 37288-61-2; 5'-inosinate phosphoribohydrolase. Cat No: EXWM-3966. | |
| Inosine | 100g Pack Size. Group: Biochemicals, Carbohydrates. Formula: C10H12N4O5. CAS No. 58-63-9. Prepack ID 51213659-100g. Molecular Weight 268.23. See USA prepack pricing. |  |
| Inosine | Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Uses: Scientific research. Category: Induced disease models products. CAS No. 58-63-9. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 25 g; 50 g; 100 g. Product ID: HY-N0092. | |
| Inosine | Inosine. Synonyms: (-)-Inosine, Hypoxanthine 9-β-D-ribofuranoside. CAS No. 58-63-9. Pack Sizes: 1, 5, 10, 25, 100 g in poly bottle. Product ID: CDC10-0576. Molecular formula: C10H12N4O5. Category: Skin protectants. Product Keywords: Cosmetic Ingredients; Active Ingredients; Skin protectants; Inosine; CDC10-0576; 58-63-9; C10H12N4O5; (-)-Inosine, Hypoxanthine 9-β-D-ribofuranoside; 200-390-4; MFCD00066770; 58-63-9. Purity: ≥99% (HPLC). EC Number: 200-390-4. Quality Level: 200. Melting Point: 222-226 °C (dec.) (lit.). | |
| Inosine | Inosine. Group: Biochemicals. Grades: Highly Purified. CAS No. 58-63-9. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. Molecular Formula: C10H12N4O5. US Biological Life Sciences. | Worldwide |
| Inosine | Inosine. Categories: inosine; 58-63-9. |  CA, FL & NJ |
| inosine-[1',2',3',4',5'-13C5] | Isotope labelled analogue of (-)-Inosine, compound that exhibits neuroprotective properties by improving axonal wiring and has also been used stroke patients treatment to restore neural function. Synonyms: [1',2',3',4',5'-13C5]inosine; inosine-1',2',3',4',5'-13C5. Grade: 98%; 99% atom 13C. Molecular formula: C5[13C]5H12N4O5. Mole weight: 273.19. | |
| Inosine-[13C2,15N] | Inosine-13C2, 15N is a labelled Inosine, which is used to treat stroke patients to restore neural function. Synonyms: Inosine-13C2,15N; (-)-Inosine-13C2,15N. Grade: > 95%. Molecular formula: C8[13C]2H12N3[15N]O5. Mole weight: 271.20. | |
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