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Catalog No. Product Name Application Product Information
A10051

Alfacalcidol

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Alfacalcidol is an analogue of vitamin D.Alfacalcidol has a weaker impact on calcium metabolism than calcitriol, while having more potent effects on parathyroid hormone levels and the immune system, including regulatory T cells.
A11676 SALE

Alibendol

-
A10054

Alizarin

CYP17 inhibitor
Alizarin is novelly used as a staining agent in biological research because it stains free calcium and certain calcium compounds a red or light purple color.
A10055

Allopurinol

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Allopurinol is a purine analog; it is a structural isomer of hypoxanthine (a naturally occurring purine in the body) and is an inhibitor of the enzyme xanthine oxidase.
A10056

Allopurinol sodium

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Allopurinol is a structural isomer of hypoxanthine (a naturally occurring purine in the body) and is an inhibitor of the enzyme xanthine oxidase.
A10057 SALE

Aloe-emodin

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Aloe emodin is a anthraquinone present in aloe latex, an exudate from the aloe plant. It has a strong stimulant-laxative action.

A10058 SALE

Aloin (Barbaloin)

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Aloin (Barbaloin) is a yellow crystalline substance obtained from aloe and is reported to be a potent inhibitors of tyrosinase.
A12432

ALPHA-ERGOCRYPTINE

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N/A
A11809 SALE

Altrenogest

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Altrenogest is a progestogen structurally related to veterinary steroid trenbolone.
A10059

Altretamine

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Altretamine is classified as an alkylating antineoplastic agent.This unique structure is believed to damage tumor cells through the production of the weakly alkylating species formaldehyde, a product of CYP450-mediated N-demethylation.
A12569

Ametantrone

topoisomerase II inhibitor
Ametantrone (AM) is a synthetic 9,10-anthracenedione bearing two (hydroxyethylamino)ethylamino residues at positions 1 and 4 along with other anthraquinones and anthracyclines.
A13167 SALE

AMG-47a

Lck inhibitor
AMG-47a is an orally bioavailable potent inhibitor of Lck and T cell proliferation. It exhibits anti-inflammatory activity (ED50 11 mg/kg) in the anti-CD3 induced production of IL-2 in mice.
A12727 SALE

AMG517

TRPV1 antagonist
AMG 517 is a potent and selective TRPV1 antagonist.
A11805 SALE

Amidopyrine

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Amidopyrine is white crystalline substance used as an analgesic and antipyretic.
A10065 SALE

Aminocaproic acid (Amicar)

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Aminocaproic acid is used to treat excessive postoperative bleeding, especially after procedures in which a great amount of bleeding is expected,
A11787 SALE

Aminopterin

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Aminopterin is an antineoplastic drug. It works as an enzyme inhibitor by competing for the folate binding site of the enzyme dihydrofolate reductase.
A10070

Ammonium Glycyrrhizinate (AMGZ)

Dehydrogenase inhibitor
Mono-ammonium glycyrrhizinate(AMGZ) is a unique product derived from Licorice root and has an extremely sweet taste.
A10072

Amorolfine HCl

Antifungal compound
Amorolfine hydrochloride, is a morpholine antifungal reagent that inhibits D14 reductase and D7-D8 isomerase, which depletes ergosterol and causes ignosterol to accumulate in the fungal cytoplasmic cell membranes.
A10073 SALE

Amphotericin B

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Amphotericin B is a polyene antifungal antibiotic from Streptomyces sp. Amphotericin B induces K+ leakage, which is separate from its lethal action, as was demonstrated in human erythrocytes and is due to the inhibitory effect on the Na+/K+ pump.
A13122

Amsilarotene (TAC-101)

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Amsilarotene (TAC-101) is a retinobenzoic acid with potential antineoplastic activity.
A10074

Amygdalin

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Amygdalin is a glycoside initially isolated from the seeds of the tree Prunus dulcis. Amygdalin induces apoptosis through regulation of Bax and Bcl-2 expressions in human DU145 and LNCaP prostate cancer cells.

A12346 SALE

Anamorelin

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Anamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
A12345

Anamorelin HCl

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Anamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
A13268 SALE

Ansamitocin P-3

microtubule depolymerizing agent
Ansamitocin P-3 is a maytansine analog which displays potent cytotoxicity against the human solid tumor cell lines A-549 and HT-29.
A12370

ANX-510

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ANX-510 is a folate-based biomodulator with potential antineoplastic activity. 5,10-methylenetetrahydrofolate (MTHF) stabilizes the covalent binding of the fluorouracil metabolite 5-5-fluoro-2'-deoxyuridine-5'-O-monophosphate (FdUMP) to its target enzyme, thymidylate synthase, which results in inhibition of thymidylate synthase, depletion of thymidine triphosphate (TTP), a necessary constituent of DNA, and tumor cell death. Unlike leucovorin, MTHF, as the active form of folate, does not require metabolic activation and may increase the chemotherapeutic effects of fluorouracil with lower toxicity.

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