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T68336Amrubicin HCl；化合物 Amrubicin HClAmrubicin HCl
Amrubicin, also known as SM-5887, is an anthracycline used in the treatment of lung cancer. Amrubicin intercalates into DNA and inhibits the activity of topoisomerase II, resulting in inhibition of DNA replication, and RNA and protein synthesis, followed by cell growth inhibition and cell death. This agent has demonstrated a higher level of anti-tumor activity than conventional anthracycline drugs without exhibiting any indication of the cumulative cardiac toxicity common to this class of compo
价 格：￥电议型 号：T68336产 地：中国大陆
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T68329HA-1004 HCl；化合物 HA-1004 HClHA-1004 HCl
HA-1004 is an inhibitor of PKA, cGKI, PKC, MYLK, and calcium channel protein.
价 格：￥电议型 号：T68329产 地：中国大陆
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T68320L594881 HCl；化合物 L594881 HClL594881 HCl
L594881, also known as 3´,4´-Dichlorobenzamil or DCB, is an inhibitor of Na+/Ca2+ exchanger, Na+ transport and sarcoplasmic reticulum Ca2+ release channels. L594881 can inhibit Na+/Ca2+ exchanger, Na+ transport and sarcoplasmic reticulum Ca2+ release channels.
价 格：￥电议型 号：T68320产 地：中国大陆
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T68308GSK-1034702 HCl；化合物 GSK-1034702 HClGSK-1034702 HCl
GSK-1034702 HCl is a potent M1 receptor allosteric agonist.
价 格：￥电议型 号：T68308产 地：中国大陆
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T6827Endoxifen Z-isomer hydrochloride；Z-因多昔芬盐酸盐Endoxifen HCl；Endoxifen HCl|||Z-因多昔芬盐酸盐
Endoxifen Z-isomer hydrochloride (Endoxifen HCl) is the active metabolite of Tamoxifen, which is an effective and selective estrogen receptor antagonist.
价 格：￥电议型 号：T6827产 地：中国大陆
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T68249IRC-083927 HCl；化合物 IRC-083927 HClIRC-083927 HCl
IRC-083927 HCl is novel and potent microtubule inhibitor with potential anticancer activity. IRC-083927 inhibits the tubulin polymerization by a binding to the colchicine site. IRC-083927 inhibits in vitro cell growth of human cancer cell lines in the low nanomolar range. More interesting, it remains highly active against cell lines resistant to microtubule-interacting agents (taxanes, Vinca alkaloids, or epothilones). Chronic oral treatment with IRC-083927 (5 mg/kg) inhibits the growth of two h
价 格：￥电议型 号：T68249产 地：中国大陆
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T68235Beclabuvir HCl；化合物 Beclabuvir HClBeclabuvir HCl
Beclabuvir, also known as BMS-791325, is an allosteric inhibitor that binds to thumb site 1 of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase. BMS-791325 inhibits recombinant NS5B proteins from HCV genotypes 1, 3, 4, and 5 at 50% inhibitory concentrations (IC50) below 28 nM. In cell culture, BMS-791325 inhibited replication of HCV subgenomic replicons representing genotypes 1a and 1b at 50% effective concentrations (EC50s) of 3 nM and 6 nM, respectively, with similar (3 to 18 nM)
价 格：￥电议型 号：T68235产 地：中国大陆
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T68227BMS-214662 HCl；化合物 BMS-214662 HClBMS-214662 HCl
BMS-214662 is a Farnesyltransferase inhibitor , is also a nonsedating benzodiazepine derivative with potential antineoplastic activity. BMS-214662 inhibits the enzyme farnesyltransferase and the post-translational farnesylation of number of proteins involved in signal transduction, which may result in the inhibition of Ras function and apoptosis in susceptible tumor cells. This agent may reverse the malignant phenotype of H-Ras-transformed cells and has been shown to be active against tumor cell
价 格：￥电议型 号：T68227产 地：中国大陆
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T68213Palonidipine HCl；化合物 Palonidipine HClPalonidipine HCl
Palonidipine HCl is a calcium channel antagonist potentially for the treatment of angina pectoris and hypertension.
价 格：￥电议型 号：T68213产 地：中国大陆
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T68194Flesinoxan HCl；化合物 Flesinoxan HClFlesinoxan HCl
Flesinoxan HCl is the salt form of Flesinoxan, which is a selective 5-HT1A receptor agonist.
价 格：￥电议型 号：T68194产 地：中国大陆
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T68182L3-Hydroxykynurenamine HCl；3-Hydroxykynurenamine 盐酸盐3-OH-Kynurenamine HCl|||3-Hydroxykynurenamine HCl
3-Hydroxykynurenamine HCl (3-OH-Kynurenamine HCl) is an immunomodulatory biogenic amine, an intermediate in the catabolism of amino acids, which induces oxidative damage and promotes cell death.
价 格：￥电议型 号：T68182L产 地：中国大陆
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T68178Neltenexine HCl；化合物 Neltenexine HClNeltenexine HCl
Neltenexine HCl is the salt form of Neltenexine free base, an elastase inhibitor that may be useful for preventing pulmonary emphysema.
价 格：￥电议型 号：T68178产 地：中国大陆
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T68171LZabicipril HCl；扎普利Zabicipril HCl(83059-56-7 Free base）|||S 9650|||S 10211；Zabicipril HCl(83059-56-7
Zabicipril HCl（S 9650） is a potent angiotensin-converting enzyme inhibitor.
价 格：￥电议型 号：T68171L产 地：中国大陆
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T68151LTallimustine HCl；他莫司汀盐酸盐Tallimustine HCl(115308-98-0 Free base)；Tallimustine HCl(115308-98-0 Free ba
Tallimustine HCl is a DNA inhibitor, an AT-specific alkylated antitumor derivative of diamycin.Tallimustine HCl can be used in severe combined immunodeficiency mouse models of adult myelogenous leukemia, which can be used for the treatment of leukemia.
价 格：￥电议型 号：T68151L产 地：中国大陆
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T6814Cyproheptadine hydrochloride；盐酸赛庚啶Periactin hydrochloride|||Anarexol|||Cyproheptadine HCl|||Nuran；Pe
Cyproheptadine hydrochloride (Periactin hydrochloride) is a hydrochloride salt form of cyproheptadine which is a histamine receptor antagonist.
价 格：￥电议型 号：T6814产 地：中国大陆
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T68135L(Rac)-Sabcomeline HCl；沙可美林盐酸盐sabcomeline HCl(149156-36-5 Free base)；sabcomeline HCl(149156-36-5 Fre
Sabcomeline HCl is an M1 receptor agonist that can be used to study Alzheimer´s disease.
价 格：￥电议型 号：T68135L产 地：中国大陆
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T68120LOt-730 HCl；Ot-730盐酸盐Ot-730 HCl(870809-51-1 Free base)；Ot-730 HCl(870809-51-1 Free base)
ot-730 HCl is a novel selective beta blocker prodrug for the study of ocular diseases.
价 格：￥电议型 号：T68120L产 地：中国大陆
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T68114LNardeterol HCl；那地特罗盐酸盐Nardeterol HCl(73865-18-6 Free base)；Nardeterol HCl(73865-18-6 Free base)
Nardeterol HCl is a β-adrenergic receptor partial agonist used in the study of the central nervous system.CAS ??13460-73-83-4
价 格：￥电议型 号：T68114L产 地：中国大陆
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T68108LMoxilubant HCl；化合物Moxilubant盐酸盐Moxilubant hcl(146978-48-5 Free base)；Moxilubant hcl(146978-48-5 Free
Moxilubant HCl is a small molecule leukotriene B4 receptor 1 (LTB4R) antagonist for the treatment of immune system disorders, skin and musculoskeletal disorders, and may be used in studies of psoriasis and rheumatoid arthritis.
价 格：￥电议型 号：T68108L产 地：中国大陆
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T68103LMk-6186 HCl；Mk-6186盐酸盐Mk-6186 HCl（1034474-19-5 Free base)；Mk-6186 HCl（1034474-19-5 Free base)
MK-6186 HCl, a novel non-nucleoside reverse transcriptase inhibitor with antiviral activity, can be used to study HIV.
价 格：￥电议型 号：T68103L产 地：中国大陆
