BOC Sciences

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BOC Sciences provides a wide variety of custom services which range from bulk compounds to specialty species in the pharmaceutical, agrochemical, and biotechnology industries. We are committed to providing our customers with the best products and services at the most competitive prices. Given diverse packing options for most of our chemicals, you are welcome to order the desired compounds in any quantities from a few mg to several kg along with all the relevant technical reports. We sincerely hope that our unremitting pursuits of excellence, success, and professionalism will add immense value to your research and development projects!

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TAS-102 50mg  | >97%

BOC Sciences

TAS-102 is a combination drug composed of the cytotoxic pyrimidine analog Trifluridine (5-trifluoro-2’-deoxythymidine or TFT) and a thymidine phosphorylase inhibitor (TPI) tipiracil hydrochloride, in a molar ratio of 1.0:0.5 (TFT:TPI). TAS-102 is used as

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TAS-103 inquire  | >98%

BOC Sciences

TAS-103, also known as BMS-247615, is a quinoline derivative that displays antitumor activity in murine and human tumor models. TAS-103 has been reported to be a potent topoisomerase II poison. TAS-103 showed the strongest antitumor activity among the con

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TAS-103 inquire  | >98%

BOC Sciences

TAS-103, also known as BMS-247615, is a quinoline derivative that displays antitumor activity in murine and human tumor models. TAS-103 has been reported to be a potent topoisomerase II poison. TAS-103 showed the strongest antitumor activity among the con

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TAS-108 inquire  | >98%

BOC Sciences

TAS-108, also known as SR16234, is a synthetic, antiestrogenic steroidal compound with potential antitumor activity. TAS-108 binds to and inhibits estrogenic receptor alpha (ERa), mainly expressed in the mammary gland and uterus and upregulated in estroge

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TAS-115 inquire  | >98%

BOC Sciences

This active molecular is a c-MET and VEGFR inhibitor which is selective and specific in vitro. In vivo studies, TAS-115 suppressed the progression of MET-inactivated tumor completely through blocking angiogenesis without toxicity and it also induced marke

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TAS-116 inquire  | >98%

BOC Sciences

TAS-116 is a inhibitor of Hsp90. It induces significant cytotoxicity in MM cells even in the presence of BMSCs, associates with downregulation of phospho-Akt and phospho-ERK. In addition, neither exogenous IL-6 nor IGF-1 was able to protect against TAS-11

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TAS-301 inquire  | >98%

BOC Sciences

TAS-301 is a potent and selective constrictive remodeling regulator on renarrowing after balloon overstretch injury of porcine coronary artery. TAS-103 inhibits smooth muscle cell migration and proliferation.

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Taselisib inquire  | >97%

BOC Sciences

Taselisib, also known as GDC0032 or RG7606, is a selective, potent, orally bioavailable inhibitor of PI3Ka with a Ki = 0.2nM, and with reduced inhibitory activity against PI3K. This selectivity profile, and excellent pharmacokinetic and pharmaceutical pro

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Tasidotin hydrochloride inquire  | >97%

BOC Sciences

Tasidotin, also know as ILX-651, is an orally active synthetic microtubule-targeted derivative of the marine depsipeptide dolastatin-15, is currently undergoing clinical evaluation for cancer treatment. Tasidotin inhibited proliferation of MCF7/GFP breas

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Tasimelteon 100mg  | >99%

BOC Sciences

Tasimelteon (trade name Hetlioz) is a drug approved by the FDA solely for the treatment of non-24-hour sleep–wake disorder (often designated as N24HSWD) in totally blind adults. It is a selective agonist for the melatonin receptors MT1 and MT2 in the supr

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Tasisulam inquire  | >98%

BOC Sciences

Tasisulam, also known as LY573636, is an acyl-sulfonamide with potential antineoplastic activity. Selectively toxic towards tumor cells, tasisulam appears to induce tumor cell apoptosis by a mitochondrial-targeted mechanism involving the loss of mitochond

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Tasosartan inquire  | >98%

BOC Sciences

Tasosartan, a pyrido-pyrimidin derivative, has been found to be an angiotensin II receptor antagonist that could have probable effect against hypertension. It has been discontinued for some security problems by Wyeth.

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TASP 0390325 inquire  | >98%

BOC Sciences

TASP 0390325 is a potent and selective vasopressin V1B receptor antagonist (IC50 = 2.22 nM for rat pituitary receptor) with no significant affinity for 85 other receptors, ion channels and transporters at 10 μM, including V1A and V2. TASP 0390325 increase

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TASP 0433864 inquire  | >98%

BOC Sciences

TASP 0433864 is a selective and positive allosteric modulator of mGlu2 receptor (EC50 = 199 and 206 nM for human and rat receptors, respectively) with no agonist activity at rat mGlu2 receptors. It displays weak activity against a range of neurotransmitte

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Taspine inquire  | >95%

BOC Sciences

Taspine, a kind of alkaloid compound, has been found to be active as immunosuppressive agent, acetilcholinesterase inhibitor as well as tumor angiogenesis inhibitor.

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Taspoglutide inquire  | >97%

BOC Sciences

Taspoglutide is a long-acting glucagon-like peptide 1 (GLP-1) receptor agonist (EC50= 0.06 nM) under investigation for treatment of type 2 diabetes.

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Tasquinimod inquire  | >98%

BOC Sciences

Tasquinimod is a quinoline-3-carboxamide linomide analogue with antiangiogenic and potential antineoplastic activities. Tasquinimod has been shown to decrease blood vessel density but the exact mechanism of action is not known. This agent has also been sh

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TAT 14 inquire  | >97%

BOC Sciences

TAT 14 is an Nrf2 activator and inhibits Nrf2/Keap1 interaction with neuroprotective activity. TAT 14 has been shown to induce upregulation of Nrf2 pathway downstream gene expression including heme-oxygenase 1 and suppress LPS-induced TNF-α expression in

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TAT-cyclo-CLLFVY inquire  | >95%

BOC Sciences

TAT-cyclo-CLLFVY has been found to be a HIF-1 dimerization inhibitor and could block protein-protein interaction of recombinant HIF-1α.

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TAT-Gap19 inquire  | >97%

BOC Sciences

TAT-Gap19 is a brain penetrating Cx43 hemichannel blocker (IC50 ~7 μM) with no significant affinity for gap junctions or Panx1 channels.

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Taurocholic acid inquire  | >96%

BOC Sciences

Taurocholic acid is a bile acid produced from the conjugation of cholic acid with taurine. It can be used as a cholagogue and cholerectic.

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Taurocholic Acid Sodium Salt Hydrate inquire  | >98%

BOC Sciences

Choleretic; Its sodium salt is a bile salt formed in the liver by conjugation of cholic acid with taurine that is involved in the emulsification of lipids used to solubilize lipids and membrane-bound proteins.

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Taurolidine inquire  | >95%

BOC Sciences

Taurolidine, an analogue of amino acid Taurine, has been found to be active as antiendotoxin and antimicrobial agent and could be used against sepsis.

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Tauroursodiol inquire  | >97%

BOC Sciences

Tauroursodiol is a bile acid formed in the liver. Tauroursodiol shows an effect of apoptosis suppression and reduction in gallstone formation.

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Tautomycetin inquire  | >95%

BOC Sciences

Tautomycetin is a selective inhibitor of protein phosphatase (PP)1 (IC50 = 1.6 and 62 nM for PP1 and PP2, respectively) used as an immunosuppressive agent. Tautomycetin induces apoptosis in activated T cells, and inhibits PDGF-induced vascular smooth musc

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Taxcultine inquire  | >97%

BOC Sciences

Taxcultine is obtained from the cell cultures of Taxus baccata. It is an impurity of Paclitaxel. It can actively promote tubulin assembly and is used in the study of function and structure microtubles into tubulin. It is a mitotic inhibitor used in cancer

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Taxezopidine L inquire  | >97%

BOC Sciences

Taxezopidine L is extracted from the seeds of the Japanese yew Taxus cuspidata Sieb. et Zucc. It could inhibit Ca2+-induced depolymerization of microtubules remarkably.

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Taxifolin inquire  | >98%

BOC Sciences

Taxifolin is a flavonoid in many plants such as Taxus chinensis, Siberian larch, Cedrus deodara and so on. Taxifolin has shown to inhibit the ovarian cancer cell growth in a dose-dependent manner.

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