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H-Tyr-Arg-Asp-Ala-P he-Leu-G lu-Pro-Leu-Phe-Arg-Asn-G lu-Leu-Ala-Tyr-Pro-Va l-Leu-Thr-Phe-Gly-N H, hydrochloride salt, > 90% 1 * 30 mg

Supplier: BACHEM BIOCHEMICA

H-Tyr-Arg-Asp-Ala-P he-Leu-G lu-Pro-Leu-Phe-Arg-Asn-G lu-Leu-Ala-Tyr-Pro-Va l-Leu-Thr-Phe-Gly-N H, hydrochloride salt, > 90% 1 * 30 mg

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1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC-HCl) 99 % Coupling reagent for peptide synthesis Empirical formula C8H17N3 . HCl Molar mass (M) 191,7 g/mol Melting point (mp)110-115 °C Solubility soluble (H2O, 20 °C) Storage temp.: - 1 * 5 g

Supplier: Roth Carl

1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC-HCl) 99 % Coupling reagent for peptide synthesis Empirical formula C8H17N3 . HCl Molar mass (M) 191,7 g/mol Melting point (mp)110-115 °C Solubility soluble (H2O, 20 °C) Storage temp.: - 1 * 5 g

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(2S,5R)-tert-Butyl 2,5-dimethylpiperazine-1-carboxylate

Supplier: Apollo Scientific

(2S,5R)-tert-Butyl 2,5-dimethylpiperazine-1-carboxylate

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2-pyrimidinemethanamine, monohydrochloride 1 * 1 g

Supplier: Cayman Chemical

2-pyrimidinemethanamine, monohydrochloride 1 * 1 g

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A tricyclic antidepressant that potently inhibits serotonin and norepinephrine reuptake (Kis = 7.4 and 96 nM, respectively) 1 * 1 g

Supplier: Cayman Chemical

A tricyclic antidepressant that potently inhibits serotonin and norepinephrine reuptake (Kis = 7.4 and 96 nM, respectively) 1 * 1 g

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An epimer of chlortetracycline 1 * 5 mg

Supplier: Cayman Chemical

An epimer of chlortetracycline 1 * 5 mg

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An epimer of chlortetracycline 1 * 500 µG

Supplier: Cayman Chemical

An epimer of chlortetracycline 1 * 500 µG

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A first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM, respectively) 1 * 5 g

Supplier: Cayman Chemical

A first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM, respectively) 1 * 5 g

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A potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 5 mg

Supplier: Cayman Chemical

A potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 5 mg

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2-Amino-5-hydroxypyridine hydrochloride_5g pack 1 * 5 g

Supplier: Apollo Scientific

2-Amino-5-hydroxypyridine hydrochloride_5g pack 1 * 5 g

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A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 5 g

Supplier: Cayman Chemical

A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 5 g

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A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 1 g

Supplier: Cayman Chemical

A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 1 g

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An inhibitor of JAK3 (IC50 = 79 nM) 1 * 10 mg

Supplier: Cayman Chemical

An inhibitor of JAK3 (IC50 = 79 nM) 1 * 10 mg

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An active metabolite of proguanil, produced by CYP2C19 1 * 5 mg

Supplier: Cayman Chemical

An active metabolite of proguanil, produced by CYP2C19 1 * 5 mg

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A first generation tricyclic antidepressant 1 * 25 g

Supplier: Cayman Chemical

A first generation tricyclic antidepressant 1 * 25 g

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1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 5 mg

Supplier: Cayman Chemical

1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 5 mg

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A -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 5 mg

Supplier: Cayman Chemical

A -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 5 mg

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Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 1 mg

Supplier: Cayman Chemical

Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 1 mg

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Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 5 mg

Supplier: Cayman Chemical

Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 5 mg

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A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 5 mg

Supplier: Cayman Chemical

A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 5 mg

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An active metabolite of proguanil, produced by CYP2C19 1 * 25 mg

Supplier: Cayman Chemical

An active metabolite of proguanil, produced by CYP2C19 1 * 25 mg

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A selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 500 mg

Supplier: Cayman Chemical

A selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 500 mg

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A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 50 mg

Supplier: Cayman Chemical

A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 50 mg

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1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 1 mg

Supplier: Cayman Chemical

1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 1 mg

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An active metabolite of proguanil, produced by CYP2C19 1 * 50 mg

Supplier: Cayman Chemical

An active metabolite of proguanil, produced by CYP2C19 1 * 50 mg

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A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 5 mg

Supplier: Cayman Chemical

A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 5 mg

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A steroidal alkaloid that suppresses NF-B signaling in LPS-stimulated macrophages, blocking induced expression of iNOS and COX-2 1 * 25 mg

Supplier: Cayman Chemical

A steroidal alkaloid that suppresses NF-B signaling in LPS-stimulated macrophages, blocking induced expression of iNOS and COX-2 1 * 25 mg

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A potent, cell-permeable inhibitor of SET7/9 (IC50 = 2 nM) that demonstrates greater than 1,000-fold selectivity over a panel of 18 other methyltransferases 1 * 5 mg

Supplier: Cayman Chemical

A potent, cell-permeable inhibitor of SET7/9 (IC50 = 2 nM) that demonstrates greater than 1,000-fold selectivity over a panel of 18 other methyltransferases 1 * 5 mg

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2-3-(2,3-dichlorophenoxy)propylamino-ethanol, monohydrochloride 1 * 5 mg

Supplier: Cayman Chemical

2-3-(2,3-dichlorophenoxy)propylamino-ethanol, monohydrochloride 1 * 5 mg

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A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 5 mg

Supplier: Cayman Chemical

A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 5 mg

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