MedChemExpress MCE - Products
MedChemExpress (MCE) offers a wide range of high-quality research chemicals and biochemicals (novel life-science reagents, reference compounds and natural compounds) for scientific use.
| Product | Description | |
|---|---|---|
| CAY 10462 dihydrochloride | CAY 10434 dihydrochloride is a potent CYP4A hydroxylase inhibitor. CAY 10434 dihydrochloride improves contractile response to angiotensin II with the maximal contractile response (E max ) 6764 mg [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 502656-68-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-120648A. |  |
| CAY10464 | CAY10464 (AHR antagonist 7; compound 4j) is a selective and high-affinity aryl hydrocarbon receptor (AhR) antagonist with a K i of 1.4 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AHR antagonist 7. CAS No. 688348-37-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-112628. | |
| Caylin-2 | Caylin-2, a Nutlin-3 analog, is a MDM2 inhibitor. Caylin-2 can bind to Bcl-X L [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1392830-09-9. Pack Sizes: 1 mg. Product ID: HY-117585. | |
| CB1 agonist 1 | CB1 agonist 1 (compound 22) is an agonist of CB1. CB1 agonist 1 shows affinity to CB1 receptor with an pIC 50 value of 5.7. CB1 agonist 1 can be used for the research of brain disorders [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 851212-80-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148137. | |
| CB1 antagonist 4 | CB1 antagonist 4 (compound 8) is a peripheral selective cannabinoid receptor type 1 (CB1) receptor antagonist. CB1 antagonist 4 shows limited penetrance to the brain in order to minimize or prevent CNS adverse reactions, and preserves potential antiobesity effects. CB1 antagonist 4 reduces propensity for psychiatric side effects [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1253641-65-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112340. | |
| CB1R antagonist 1 | CB1R Allosteric modulator 5, a selective cannabinoid-1 receptor (CB1R) inverse agonist with an IC 50 value of 4.2 μM and EC 50 value of ?10 μM. CB1R Allosteric modulator 5 can be used for the research of metabolic and obesity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 334668-69-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-150067. | |
| CB-25 | CB-25 is a ligand of CB1 cannabinoid receptors , acting as a partial agonist. CB-25 enhances Forskolin (HY-15371)-induced cAMP formation in cancer cells but not hCB1-CHO cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 869376-63-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121541. | |
| CB2 receptor agonist 10 | CB2 receptor agonist 10 is a CB2 receptor agonist with a K i of 3.7 nM for hCB2 , a K i of 110 nM for hCB1 , and an EC 50 of 0.52 nM for hCB2 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1046140-32-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-113591. | |
| CB2 receptor agonist 2 | CB2 receptor agonist 2 is a potent and selective agonist for the CB2 (cannabinoid type 2) receptor with a K i of 8.5 nM. CB2 receptor agonist 2 has high affinity and selectivity for CB2 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1314230-75-5. Pack Sizes: 5 mg. Product ID: HY-132217. | |
| CB-5083 | CB-5083 is a first-in-class, potent, selective, and orally bioavailable inhibitor of the p97 AAA ATPase / VCP. CB-5083 selectively inhibits p97 through its D2 site with the IC 50 of 11 nM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1542705-92-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12861. | |
| CB-5339 | CB-5339 is an oral activity potent p97 inhibitor with an IC 50 <30 nM. CB-5339 can be used for leukemia research [1]. CB-5339 extracted from WO2015109285A1 compound FF07. Uses: Scientific research. Group: Signaling pathways. CAS No. 1863952-15-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-128724. | |
| CBL0137 | CBL0137, a curaxin compound, is a histone chaperone facilitates chromatin transcription (FACT) inhibitor. CBL0137 downregulates NF- B and activates p53. CBL0137 restores both histone H3 acetylation and trimethylation. CBL0137 is an anticancer agent. CBL0137 induces cancer cell apoptosis [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Curaxin 137; CBL-C137. CAS No. 1197996-80-7. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18935. | |
| CBL0137 hydrochloride | CBL0137 hydrochloride is an inhibitor of the histone chaperone, FACT. CBL0137 hydrochloride can also activate p53 and inhibits NF-κB with EC 50 s of 0.37 and 0.47 μM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Curaxin-137 hydrochloride; CBL-C137 hydrochloride. CAS No. 1197397-89-9. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18935A. | |
| CBP/p300-IN-19 hydrochloride | CBP/p300-IN-19 hydrochloride is a potent and selective p300/CBP HAT inhibitor with IC 50 s of 1.4, 2.2, >100, >100 μM for p300-HAT, CBP-HAT, PCAF, Myst3, respectively. CBP/p300-IN-19 hydrochloride shows antitumor activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2592638-14-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-146277A. | |
| CC-90002 | CC-90002 is a humanized anti-CD47 monoclonal antibody (mAb). CC-90002 has a high affinity for binding to CD47 with a subnanomolar K d value. CC-90002 can be used for the research of hematologic malignancies and solid tumors [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2085844-54-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99172. | |
| CC-90003 | CC-90003 is an irreversible and selective inhibitor of ERK 1/2 with antitumor activity. Uses: Scientific research. Group: Signaling pathways. CAS No. 1621999-82-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112570. | |
| CCCP | CCCP is an oxidative phosphorylation ( OXPHOS ) uncoupler. CCCP induces activation of PINK1 leading to Parkin Ser65 phosphorylation [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Carbonyl cyanide 3-chlorophenylhydrazone; Carbonyl Cyanide m-Chlorophenylhydrazone. CAS No. 555-60-2. Pack Sizes: 10 mM * 1 mL; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-100941. | |
| CCG-1423 | CCG-1423 is an inhibitor of Rho/MRTF/SRF pathway. CCG-1423 shows activities in several cancer cells. CCG-1423 is a promising lead compound for the development of novel pharmacologic tools, and it can be used for the research of cancer and diabetes [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 285986-88-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-13991. | |
| CCG273441 | CCG273441 is a covalent inhibitor of G protein-coupled receptor ( GPCR ) kinase 5 ( GRK5 ) with an IC 50 value of 3.8 nM. CCG273441 is highly selective to GRK5 over GRK2 (IC 50 =4.8 μM) by binding Cys474, a GRK5 subfamily-specific residue, as a covalent handle [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2750414-35-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-47573. | |
| CCMI | CCMI (AVL-3288) is a potent and selective α7 nAChR -positive allosteric modulator, does not bind to or activate α7 nAChRs via the orthosteric site, and causes significant positive modulation of agonist-induced currents at α7 nAChRs. CCMI has potential in CNS diseases with cognitive dysfunction [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AVL-3288; UCI-4083. CAS No. 917837-54-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-12150. | |
| CCPA | CCPA (2-Chloro-N6-cyclopentyladenosine) is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis , etc [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 2-Chloro-N6-cyclopentyladenosine. CAS No. 37739-05-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-103185. | |
| CCT241533 hydrochloride | CCT241533 hydrochloride is a potent and selective CHK2 inhibitor with an IC 50 of 3 nM and a K i of 1.16 nM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1431697-96-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14715B. | |
| CCT245232 | CCT245232 is a potent inhibitor of heat shock factor 1 ( HSF1 ). HSF1 is the master regulator of the heat shock response, in which multiple genes are induced in response to temperature increase and other stresses. CCT245232 has the potential for the research of proliferative diseases, such as cancer (extracted from patent WO2015049535A1) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1693731-14-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-144867. | |
| CCT374705 | CCT374705 is an orally active BCL6 inhibitor with potent antiproliferative effects in vitro. CCT374705 effectively inhibits tumor growth in a lymphoma xenograft mouse model [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2640647-90-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153521. | |
| CD2665 | CD2665 is an orally active and selective RAR-β,γ antagonist, with K d values of 306 nM, 110 nM for RAR-β and RAR-γ, repectively [1] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 170355-78-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-107437. | |
| CD31 | CD31 (PECAM-1) is platelet endothelial cell adhesion molecule-1, serves as the endothelial cell-specific receptor of clostridium perfringens b-Toxin ( CPB ). CD31 is also an ER-MP12 antigen , acts as a linker between mechanical stress, metabolism and inflammation. CD31 peptide is able to sustain phosphorylation of the CD31 ITIM 686 and of SHP2 and to inhibit TCR -induced T-cell activation [1] - [5]. Uses: Scientific research. Group: Peptides. Alternative Names: PECAM-1. CAS No. 161374-99-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P3444. | |
| CD437 | CD437 is a selective Retinoic Acid Receptor γ (RARγ) agonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AHPN. CAS No. 125316-60-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100532. | |
| CD532 | CD532 is a potent Aurora A kinase inhibitor with an IC 50 of 45 nM. CD532 has the dual effect of blocking Aurora A kinase activity and driving degradation of MYCN. CD532 also can directly interact with AURKA and induces a global conformational shift. CD532 can be used for the research of cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1639009-81-6. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-112273. | |
| CD532 hydrochloride | CD532 hydrochloride is a potent Aurora A kinase inhibitor with an IC 50 of 45 nM. CD532 hydrochloride has the dual effect of blocking Aurora A kinase activity and driving degradation of MYCN. CD532 hydrochloride also can directly interact with AURKA and induces a global conformational shift. CD532 hydrochloride can be used for the research of cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2926498-81-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-112273A. | |
| CDAP | CDAP is an organic cyanylating reagent that can be used for preparation of solid phase affinity reagents, modification of protein thiols and nucleotide delivery. CDAP also activates polysaccharides with a variety of chemical properties. CDAP can be used to prepare conjugate vaccines and other immune reagents [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 59016-56-7. Pack Sizes: 100 mg. Product ID: HY-W012184. | |
| CDDO-Im | CDDO-Im (RTA-403) is an activator of Nrf2 and PPAR , with K i s of 232 and 344 nM for PPARα and PPARγ [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RTA-403; TP-235; CDDO-Imidazolide. CAS No. 443104-02-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15725. | |
| CDFI | CDFI is an inhibitor of the lipid II flippase MurJ. CDFI potentiates the activity of β-lactams against MRSA [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1199797-92-6. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-156009. | |
| CDK2 | CDK2 is a member of the eukaryotic S/T protein kinase family and its function is to catalyze the phosphoryl transfer of ATP γ-phosphate to serine or threonine hydroxyl (denoted as S 0 /T 0 ) in a protein substrate. Uses: Scientific research. Group: Peptides. CAS No. 255064-79-0. Pack Sizes: 5 mg. Product ID: HY-P0235. | |
| CDK2-IN-30 | CDK2-IN-30 (Formula (I)) is a CDK2 inhibitor with an IC 50 value ≤20 nM. CDK2-IN-30 can be used in tumor research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2640038-22-6. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-164664. | |
| CDK4/6-IN-15 | CDK4/6-IN-15 is an orally active and selective CDK4/6 inhibitor. CDK4/6-IN-15 potently inhibits cancer cells growth. CDK4/6-IN-15 arrests cell cycle at G1 phase and suppresses retinoblastoma tumour suppressor protein (Rb) phosphorylation at S780 and E2 factor (E2F)-regulated gene expression [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2078047-99-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-142076. | |
| Cdk5 Substrate | Cdk5 Substrate is a biological active peptide. (substrate for the cdc2 protein kinase). Uses: Scientific research. Group: Peptides. CAS No. 164669-07-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2668. | |
| CDK7-IN-2 | CDK7-IN-2 is a potent inhibitor of CDK7. CDK7 is implicated in both temporal control of the cell cycle and transcriptional activity. CDK7 is implicated in the transcriptional initiation process by phosphorylation of Rbpl subunit of RNA Polymerase II (RNAPII). CDK7 has the potential for the research of cancer disease, in particular aggressive and hard- to-treat cancers (extracted from patent WO2019099298A1, compound 1) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2326428-19-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-143587. | |
| CDK8-IN-13 | CDK8-IN-13 is a potent, selective and orally active CDK8 inhibitor with an IC 50 value of 51.9 nM. CDK8-IN-13 induces Apoptosis. CDK8-IN-13 decreases the expression of p-STAT1 S727 and p-STAT5 S726. CDK8-IN-13 shows antitumor activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 918523-75-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-149974. | |
| CDK9-IN-14 | CDK9-IN-14 is a potent and selective CDK9 inhibitor with IC 50 of 6.92 nM. CDK9-IN-14 has a relatively strong inhibitory effect on MV4;11 cells and in vivo tumor models, and has a good selectivity and a low toxicity and few side effects [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2650640-17-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-143585. | |
| CDK9-IN-30 | CDK9-IN-30 is a CDK9 inhibitor that inhibits HIV-1 viral replication [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 748146-89-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-147131. | |
| CDK9-IN-34 | CDK9-IN-34 (Compound 1b) is an inhibitor for CDK9 with an IC 50 of 0.25 μM. CDK9-IN-34 exhibits cytotoxicity to cancer cell HCT116, MCF7 and K652 with IC 50 of 1.43, 3.01 and 50.27 μM, respectively. CDK9-IN-34 exhibits antiviral activity against coronavirus 229E with an IC 50 of 145.92 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 252725-86-3. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-164619. | |
| CDPPB | CDPPB is a selective, orally active mGluR5 allosteric modulator. CDPPB increases AKT and ERK1/2 activation and augments the BDNF mRNA. CDPPB inhibits caspase-3 activation and mitochondrial dysfunction. CDPPB improves cognitive impairment, depression, and Huntington's disease [1] [2] [3] [4] [5] [6] [7] [8] [9]. Uses: Scientific research. Group: Signaling pathways. CAS No. 781652-57-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14569. | |
| Cebranopadol | Cebranopadol is an analgesic NOP and opioid receptor agonist with K i s/ EC 50 s of 0.9 nM/13 nM, 0.7 nM/1.2 nM, 2.6 nM/17 nM, 18 nM/110 nM for human NOP, MOP, KOP and delta-opioid peptide (DOP) receptor, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GRT6005. CAS No. 863513-91-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-15536. | |
| Cecropin A | Cecropin A is a linear 37-residue antimicrobial polypeptide, with anticancer and anti-inflammatory activity. Uses: Scientific research. Group: Peptides. CAS No. 80451-04-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1539. | |
| Cecropin A (1-7)-Melittin A (2-9) | Cecropin A (1-7)-Melittin A (2-9) is an antimicrobial peptide with antimicrobial activity against a broad spectrum of Gram-positive and Gram-negative aerobic bacteria, as well as antimalarial activity, without the adverse hemolytic properties of bee venom peptides [1]. Uses: Scientific research. Group: Peptides. Alternative Names: Oct-CA(1-7)M(2-9). CAS No. 157606-25-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P3914. | |
| Cecropin B | Cecropin B has high level of antimicrobial activity and is considered as a valuable peptide antibiotic. Uses: Scientific research. Group: Peptides. CAS No. 80451-05-4. Pack Sizes: 500 μg; 1 mg; 5 mg; 10 mg. Product ID: HY-P0092. | |
| Cecropin P1, porcine | Cecropin P1, porcine is an antibacterial peptide that can be isolated from the upper part of the small intestine of the pig. Cecropin P1, porcine shows antibacterial activity against Gram-negative bacteria. Cecropin P1, porcine shows antiviral activity and inhibits PRRSV infection [1] [2]. Uses: Scientific research. Group: Peptides. CAS No. 125667-96-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P2317. | |
| Cedar oil | Cedar oil is an essential oil that can be extracted from numerous types of conifers. Cedar oil possesses some pesticidal properties. As a food additive and preservative, cedarwood oil is a blend of organic chemicals classified as safe compounds by the FDA. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Oils, cedarwood. CAS No. 8000-27-9. Pack Sizes: 25 g. Product ID: HY-W133894. | |
| Cedarwood terpenes | Cedarwood terpenes is a natural terpene mixture that can be extracted from cedar wood [1]. Uses: Scientific research. Group: Natural products. CAS No. 68608-32-2. Pack Sizes: 25 mg; 50 mg. Product ID: HY-W794998. | |
| Cedazuridine | Cedazuridine (E7727) (Compound 7a) is an orally active cytidine deaminase (CDA) inhibitor with an IC 50 value of 0.4 μM. Cedazuridine can be used for cancer research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: E7727. CAS No. 1141397-80-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109081. | |
| Cediranib | Cediranib (AZD2171) is a highly potent, orally available VEGFR tyrosine kinase inhibitor with IC 50 s of <1, <3, 5, 5, 36, 2 nM for Flt1, KDR, Flt4, PDGFRα, PDGFRβ, c-Kit, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD2171. CAS No. 288383-20-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10205. | |
| Cediranib maleate | Cediranib maleate (AZD-2171 maleate) is a highly potent, orally available VEGFR inhibitor with IC 50 s of <1, <3, 5, 5, 36, 2 nM for Flt1, KDR, Flt4, PDGFRα, PDGFRβ, c-Kit, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD-2171 maleate. CAS No. 857036-77-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13049. | |
| Cedirogant | Cedirogant (ABBV-157) is an orally active RORγt inverse agonist. Cedirogant can be used for psoriasis research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABBV-157. CAS No. 2055496-11-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-137434. | |
| (-)-Cedrene | (-)-Cedrene (α-cedrene) is a sesquiterpene constituent of cedarwood oils, with anti-leukemic, antimicrobial and anti-obesity activities [1]. Uses: Scientific research. Group: Natural products. Alternative Names: α-cedrene. CAS No. 469-61-4. Pack Sizes: 1 mL; 10 mM * 1 mL; 5 mL. Product ID: HY-135190. | |
| Cedrol | Cedrol is a potent competitive inhibitor of cytochrome P-450(CYP) enzyme. Cedrol plays an anticancer role by inducing cell cycle arrest and Caspase-dependent apoptosis. Cedrol acts as a neutrophil agonist that can desensitize cells to subsequent stimulation of N-formyl peptides. Cedrol prevents neuropathic pain caused by chronic contractile injury by inhibiting oxidative stress and inflammation. In addition, Cedrol has antibacterial, hair loss prevention and anti-anxiety properties [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Natural products. Alternative Names: (+)-Cedrol; α-Cedrol. CAS No. 77-53-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N2071. | |
| Cedryl acetate | Cedryl acetate is a tricyclic sesquiterpene isolated from the plant Cunninghamia lanceolata. Cedryl acetate shows α-glucosidase inhibitory activity [1]. Uses: Scientific research. Group: Natural products. CAS No. 77-54-3. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W009417. | |
| Cefaclor | Cefaclor is a well-absorbed orally active cephalosporin antibiotic. Cefaclor can specifically bind to specific for penicillin-binding protein 3 ( PBP3 ). Cefaclor can be used for the research of depression and kinds of infections caused by bacteria, such as respiratory tract infections, bacterial bronchitis, pharyngitis and skin infections [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 53994-73-3. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0198. | |
| Cefaclor monohydrate | Cefaclor is a well-absorbed orally active cephalosporin antibiotic. Cefaclor can specifically bind to specific for penicillin-binding protein 3 ( PBP3 ). Cefaclor can be used for the research of depression and kinds of infections caused by bacteria, such as respiratory tract infections, bacterial bronchitis, pharyngitis and skin infections [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 70356-03-5. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B0198A. | |
| Cefadroxil | Cefadroxil is a broad-spectrum antibiotic of the cephalosporin type, effective in Gram-positive and Gram-negative bacterial infections. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BL-S 578. CAS No. 50370-12-2. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg. Product ID: HY-B1190. | |
| Cefadroxil hydrate | Cefadroxil hydrate (BL-S 578 hydrate) is an orally active and first-generation cephalosporin with a broad spectrum antibacterial activity. Cefadroxil hydrate (BL-S 578 hydrate) also acts as a substrate of the peptide transporter PEPT1 and PEPT2 [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BL-S 578 hydrate. CAS No. 66592-87-8. Pack Sizes: 100 mg. Product ID: HY-B1190A. | |
| Cefadroxil (Standard) | Cefadroxil (Standard) is the analytical standard of Cefadroxil. This product is intended for research and analytical applications. 0. Uses: Scientific research. Group: Signaling pathways. CAS No. 50370-12-2. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1190R. | |
| Cefamandole nafate | Cefamandole nafate (Cefamandole formate sodium) is a second-generation broad-spectrum cephalosporin antibiotic [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefamandole formate sodium. CAS No. 42540-40-9. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B1166. | |
| Cefamandole sodium | Cefamandole Sodium Salt is a second-generation broad-spectrum cephalosporin antibiotic. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cephamandole sodium. CAS No. 30034-03-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-B1128A. | |
| Cefazedone | Cefazedone (Refosporen), a first-generation cephalosporin, is a time-dependent antibiotic with activity against Gram-positive and Gram-negative bacteria [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Refosporen. CAS No. 56187-47-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121144. | |
| Cefazolin | Cefazolin (Cephazolin) is a first-generation cephalosporin antibiotic and can be used in varieties of bacterial infections research [1]. Cefazolin has anti-inflammatory effect and can attenuate post-operative cognitive dysfunction (POCD) [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cephazolin. CAS No. 25953-19-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1892. | |
| Cefazolin sodium | Cefazolin sodium is a first-generation cephalosporin antibiotic and can be used in varieties of bacterial infections research [1]. Cefazolin sodium has anti-inflammatory effect and can attenuate post-operative cognitive dysfunction (POCD) [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cephazolin sodium. CAS No. 27164-46-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1078. | |
| Cefcapene pivoxil hydrochloride | Cefcapene pivoxil hydrochloride, the pivalate ester prodrug form of Cefcapene, is an orally active third-generation cephalosporin with a wide spectrum of anti-bacterial activity. Cefcapene pivoxil hydrochloride has the potential for the palmoplantar pustulosis (PPP) research [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 147816-23-7. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-135221. | |
| Cefdinir | Cefdinir (FK-482) is a semi-synthetic, broad-spectrum antibiotic in the third generation of the cephalosporin class, which is proved to be effective for infections caused by several Gram-negative and Gram-positive bacteria. Cefdinir can be used for the research of common bacterial infections of the ear, sinus, throat, and skin [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FK-482; CI-983. CAS No. 91832-40-5. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B0136. | |
| Cefditoren | Cefditoren is an orally active antibiotic with broad-spectrum antibacterial activity, capable of inhibiting both Gram-negative and Gram-positive bacteria. It has a MIC 50 of 0.25-0.5 mg/L against Streptococcus pneumoniae strains. Cefditoren is effective against respiratory tract infections and skin infections [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 104145-95-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-159688. | |
| Cefditoren Pivoxil | Cefditoren Pivoxil (ME 1207) is a broad-spectrum, third-generation, oral cephalosporin antibacterial with enhanced stability against many common β lactamases. Cefditoren Pivoxil has activity against Gram-negative organisms and Gram-positive organisms. Cefditoren Pivoxil can be used in the research of infection diseases such as acute exacerbations of chronic bronchitis, community-acquired pneumonia (CAP), streptococcal pharyngitis/tonsillitis, or uncomplicated skin and skin structure infections [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefditoren pivoxyl; Cefditoren pivaloyloxymethyl ester; ME 1207. CAS No. 117467-28-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-17452A. | |
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