A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
ZCZ011 is a potent and brain-penetrant cannabinoid 1 (CB1) receptor positive allosteric modulator. ZCZ011 potentiates binding of CP55,940 to the CB1 receptor, enhances anandamide (AEA)-stimulated GTPγS binding in mouse brain membranes. ZCZ011 increases β-arrestin recruitment and ERK phosphorylation in hCB1 cells. ZCZ011 can be used for researching neuropathic and inflammatory pain[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1998197-39-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-118140.
ZD06519
ZD06519 (7-Hydroxyethyl carbamate-(10Me-11F-Camptothecin)) is a camptothecin (HY-16560) analogue and a topoisomerase I inhibitor. ZD06519 is an ADC cytotoxin with a strong bystander effect, inhibiting a variety of malignancies such as HER2-positive and FRα-overexpressing tumors. ZD06519 inhibits DNA cleavage, relaxation, and reconnection processes, inducing tumor cell death. ZD06519 can be used for ADC synthesis and cancer research[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 7-Hydroxyethyl carbamate-(10Me-11F-Camptothecin). CAS No. 2873460-17-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-156513.
ZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antagonist. Uses: Scientific research. Category: Signaling pathways. CAS No. 146709-78-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-102093.
ZD7288
ZD7288 (ICI D7288) is a selective hyperpolarization-activated cyclic nucleotide-gated (HCN) channel blocker[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ICI D7288. CAS No. 133059-99-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101346.
ZD 7288
ZD 7288 is a selective Ih channel inhibitor. ZD 7288 is an sino-atrial node function modulator; blocks the hyperpolarization activated cation current If. ZD 7288 blocks Ih in central neurons. ZD 7288 increases NMDA-evoked noradrenalin release in rat brain in vitro. Group: Biochemicals. Alternative Names: N-Ethyl-1,6-dihydro-1,2-dimethyl-6-(methylimino)-N-phenyl-4-pyrimidinamine Hydrochloride; N-Ethyl-1,6-dihydro-1,2-dimethyl-6-(methylimino)-N-phenyl-4-pyrimidinamine Monohydrochloride; ICI-D 7288. Grades: Highly Purified. CAS No. 133059-99-1. Pack Sizes: 5mg, 10mg, 25mg. Molecular Formula: C??H??ClN?, Molecular Weight: 292.81. US Biological Life Sciences.
Worldwide
Z-D-Ala-Gly-OH
Z-D-Ala-Gly-OH. Synonyms: (R)-2-(2-(((Benzyloxy)carbonyl)amino)propanamido)acetic acid; Z D Ala Gly OH. Grade: ≥ 95% (HPLC). CAS No. 34286-66-3. Molecular formula: C13H16N2O5. Mole weight: 280.28.
Z-D-Ala-Gly-OH
Z-D-Ala-Gly-OH. Group: Biochemicals. Grades: Highly Purified. CAS No. 34286-66-3. Pack Sizes: 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
Z-D-Ala-Gly-OH ≥95% (HPLC)
Z-D-Ala-Gly-OH ≥95% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 2.5g, 5g. US Biological Life Sciences.
Z-D-Arg-Gly-Arg-pNA 2HCl is a chromogenic substrate for determining factor Xa. Synonyms: L-Argininamide, N2-[(Phenylmethoxy)carbonyl]-D-arginylglycyl-N-(4-nitrophenyl)-, Dihydrochloride; N2-[(Benzyloxy)carbonyl]-D-arginylglycyl-N-(4-nitrophenyl)-L-argininamide hydrochloride (1:2); Z-RGR-pNA; Benzyl-D-Arg-Gly-Arg-pNA dihydrochloride; Benzyl-D-Arg-Gly-Arg-p-nitroanilide dihydrochloride; Factor Xa Chromogenic Substrate dihydrochloride; S-2765 dihydrochloride. Grade: 95%. CAS No. 113711-77-6. Molecular formula: C28H39N11O7.2HCl. Mole weight: 714.61.
Z-D-Asn(Xan)-OH
Z-D-Asn(Xan)-OH. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
Z-D-aspartic acid
Z-D-aspartic acid. Uses: A competitive inhibitor of indole-3-acetyl-l-aspartic acid hydrolase of enterobacter agglomerans. Synonyms: Z-D-Asp-OH; (R)-2-(((Benzyloxy)Carbonyl)Amino)Succinic Acid. Grade: ≥ 98% (HPLC). CAS No. 78663-07-7. Molecular formula: C12H13NO6. Mole weight: 267.20.
Z-D-aspartic acid 99+%
Z-D-aspartic acid 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences.
Worldwide
Z-D-aspartic acid b-allyl ester 98+% (HPLC)
Z-D-aspartic acid b-allyl ester 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences.
Worldwide
Z-D-aspartic acid b-benzyl ester 99+%
Z-D-aspartic acid b-benzyl ester 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
Z-D-aspartic acid β-allyl ester
A useful building block in the synthesis of various pharmaceuticals. Synonyms: Z-D-Asp(OAll)-OH; N-[(Phenylmethoxy)carbonyl]-D-aspartic Acid 4-(2-Propen-1-yl) Ester. Grade: ≥ 98% (HPLC). CAS No. 1272755-66-4. Molecular formula: C15H17NO6. Mole weight: 307.20.
Z-dehydroalanine methyl ester 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
Z-DEVD-FMK
Z-DEVD-FMK is a cell-permeant, irreversible caspase-3 inhibitor that can be used as an anaesthetic agent. It has been shown to suppress tumor cell apoptosis. Uses: Cysteine proteinase inhibitors. Synonyms: Z-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-FMK; Caspase-3 Inhibitor; Z-D(OMe)E(Ome)VD(OMe)-FMK; benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-fluoromethylketone; Caspase-3 Inhibitor II; Z-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-Fluoromethylketone; Z-DEVD-fluoromethylketone. Grade: ≥95%. CAS No. 210344-95-9. Molecular formula: C30H41FN4O12. Mole weight: 668.67.
Z-DEVD-FMK
Z-DEVD-FMK (Caspase-3 Inhibitor) is a specific, irreversible Caspase-3 inhibitor, and also shows potent inhibition on caspase-6, caspase-7, caspase-8, and caspase-10. Group: Inhibitors. Alternative Names: Caspase-3 Inhibitor. CAS No. 210344-95-9. Pack Sizes: 1mg. Product ID: S7312. Formula: C30H41FN4O12. Smiles: CC(C)C(C(=O)NC(CC(=O)OC)C(=O)CF)NC(=O)C(CCC(=O)OC)NC(=O)C(CC(=O)OC)NC(=O)OCC1=CC=CC=C1. Storage Conditions: 2 years -80 in solvent.
United States; Europe
Z-DEVD-FMK
Z-DEVD-FMK is a specific and irreversible caspase-3 inhibitor with an IC50 of 18 μM[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 210344-95-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-12466.