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T15760LLintopride HCl；Lintopride 盐酸盐Lintopride HCl（107429-63-0 Free base)；Lintopride HCl（107429-63-0 Free b
Lintopride HCl is a 5HT-4 antagonist.
价 格：￥电议型 号：T15760L产 地：中国大陆
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T1574LEtoricoxib HCl；化合物 T1574LL-791456 monohydrochloride salt|||L791456 hydrochloride|||L-791456 hydrochl
Etoricoxib HCl is a synthetic, nonsteroidal anti-inflammatory drug. Etoricoxib specifically binds to and inhibits the enzyme cyclooxygenase-2, resulting in inhibition of the conversion of arachidonic acid into prostaglandins.
价 格：￥电议型 号：T1574L产 地：中国大陆
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T1549Raloxifene hydrochloride；盐酸雷洛昔芬LY156758 hydrochloride|||Raloxifene HCl|||LY139481 hydrochloride|||Ke
Raloxifene hydrochloride (LY156758 hydrochloride) is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. It has estrogen agonist effects on bone and cholesterol metabolism but behaves as a complete estrogen antagonist on mammary gland and uterine tissue.
价 格：￥电议型 号：T1549产 地：中国大陆
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T15465HC-070；化合物HC-070HC 070；HC 070
HC-070 is a TRPC5 and TRPC4 antagonist (IC50 = 9.3 nM and 46 nM).
价 格：￥电议型 号：T15465产 地：中国大陆
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T1543Naftifine hydrochloride；盐酸萘替芬Naftifungin|||Naftifine HCl|||Naftin|||Exoderil；Naftifungin|||盐酸萘替芬|||N
Naftifine Hydrochloride is the hydrochloride salt form of naftifine, an allylamine derivate with synthetic broad-spectrum antifungal activity. Although the exact mechanism through which naftifine hydrochloride exerts its effect is unknown, it appears to selectively inhibit the enzyme squalene 2, 3-epoxidase, thereby inhibiting the biosynthesis of sterol. This results in a decreased amount of sterols, especially ergosterol which is the primary fungal membrane sterol, and a corresponding accumulat
价 格：￥电议型 号：T1543产 地：中国大陆
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T1542Pirenzepine dihydrochloride；盐酸哌仑西平Pirenzepine HCl|||Bisvanil|||Tabe|||LS519；Pirenzepine HCl|||Bisvan
Pirenzepine dihydrochloride (LS519) is a selective M1 muscarinic receptor antagonist, inhibiting gastric secretion.
价 格：￥电议型 号：T1542产 地：中国大陆
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T1540Doxepin hydrochloride；盐酸多塞平Toruan|||Doxepin HCl|||Aponal|||Novoxapin；Toruan|||Doxepin HCl|||Aponal||
Doxepin hydrochloride (Aponal) is a dibenzoxepin tricyclic compound. It displays a range of pharmacological actions including maintaining adrenergic innervation. Its mechanism of action is not fully understood, but it appears to block reuptake of monoaminergic neurotransmitters into presynaptic terminals. It also possesses anticholinergic activity and modulates antagonism of histamine H(1)- and H(2)-receptors.
价 格：￥电议型 号：T1540产 地：中国大陆
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T1533Valganciclovir hydrochloride；缬更昔洛韦盐酸盐Valganciclovir HCl|||Valcyt|||Valcyte；Valganciclovir HCl|||Valc
Valganciclovir hydrochloride (Valganciclovir HCl) is a hydrochloride salt form of valganciclovir, a prodrug form of ganciclovir, a nucleoside analog of 2´-deoxyguanosine, with antiviral activity. After phosphorylation, valganciclovir is incorporated into DNA, resulting in inhibition of viral DNA polymerase, and viral replication.
价 格：￥电议型 号：T1533产 地：中国大陆
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T1528Azasetron hydrochloride盐酸阿扎司琼Y-25130 hydrochloride|||Y-25130 HCl|||盐酸阿扎司琼|||Azasetron HCl
Azasetron hydrochloride (Y-25130 HCl) is a 5-HT3 receptor antagonist which is used as an anti-emetic.
价 格：￥电议型 号：T1528产 地：中国大陆
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T1517Benserazide hydrochloride；盐酸苄丝肼Benserazide HCl|||Serazide|||Ro 4-4602；Benserazide HCl|||盐酸苄丝肼|||Sera
Benserazide hydrochloride (Ro 4-4602) is a peripherally-acting L-amino acid decarboxylase (AAAD) or DOPA decarboxylase inhibitor.
价 格：￥电议型 号：T1517产 地：中国大陆
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T1511Daunorubicin hydrochloride；盐酸柔红霉素Daunomycin HCl|||RP-13057 Hydrochloride|||Rubidomycin hydrochloride
Daunorubicin hydrochloride (Rubidomycin hydrochloride) is an anthracycline aminoglycoside, a topoisomerase II (Topo II) inhibitor. Daunorubicin hydrochloride inhibits DNA and RNA synthesis and has antitumor activity.
价 格：￥电议型 号：T1511产 地：中国大陆
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T15065DBCO-NHCO-PEG5-NHS ester；化合物 T15065DBCO-NHCO-PEG5-NHS ester
DBCO-NHCO-PEG5-NHS ester is a polyethylene glycol (PEG)-based linker utilized in the synthesis of PROTACs[1].
价 格：￥电议型 号：T15065产 地：中国大陆
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T15064DBCO-NHCO-PEG4-NHS ester；化合物 T15064DBCO-NHCO-PEG4-NHS ester
DBCO-NHCO-PEG4-NHS ester ester is a MMP-2- and cathepsin B- (CatB) cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15064产 地：中国大陆
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T15063DBCO-NHCO-PEG4-NH-Boc；化合物 T15063DBCO-NHCO-PEG4-NH-Boc
DBCO-NHCO-PEG4-NH-Boc is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15063产 地：中国大陆
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T15062DBCO-NHCO-PEG4-amine；化合物 T15062DBCO-NHCO-PEG4-amine
DBCO-NHCO-PEG4-amine is a cleavable ADC linker used to conjugate MMAE and antibody (e.g., DBCO-VCpAB MMAE and DBCO-TRX MMAE with EC50s of 280 nM and 22 nM in SKBR3 cells, respectively)[1].
价 格：￥电议型 号：T15062产 地：中国大陆
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T15061DBCO-NHCO-PEG4-acid；化合物 T15061DBCO-NHCO-PEG4-acid
DBCO-Amide-PEG5-acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15061产 地：中国大陆
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T1496Amiodarone hydrochloride；盐酸胺碘酮Amiodar|||Amiodarone HCl|||Nexterone；盐酸胺碘酮|||Amiodar|||Amiodarone HCl|
Amiodarone hydrochloride (Amiodarone HCl) is an antianginal and class III antiarrhythmic drug. It increases the duration of ventricular and atrial muscle action by inhibiting POTASSIUM CHANNELS and VOLTAGE-GATED SODIUM CHANNELS. There is a resulting decrease in heart rate and in vascular resistance.
价 格：￥电议型 号：T1496产 地：中国大陆
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T1488Procarbazine hydrochloride；盐酸甲基苄肼NSC-77213 HCl|||Procarbazine HCl；NSC-77213 HCl|||盐酸甲基苄肼|||Procarbaz
Procarbazine hydrochloride (NSC-77213 HCl) is the hydrochloride salt of a methylhydrazine derivative with antineoplastic and mutagenic activities. Although the exact mode of cytotoxicity has not been elucidated, procarbazine, after metabolic activation, appears to inhibit the trans-methylation of methionine into transfer RNA (t-RNA), thereby preventing protein synthesis and consequently DNA and RNA synthesis. This agent may also undergo auto-oxidation, resulting in the formation of cytotoxic fre
价 格：￥电议型 号：T1488产 地：中国大陆
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T1471Duloxetine hydrochloride；盐酸度洛西汀Duloxetine HCl|||LY-248686 hydrochloride|||(S)-Duloxetine hydrochlori
Duloxetine hydrochloride ((S)-Duloxetine hydrochloride) is a thiophene derivative and selective neurotransmitter uptake inhibitor for SEROTONIN and NORADRENALINE (SNRI). It is an ANTIDEPRESSIVE AGENT and ANXIOLYTIC and is also used for the treatment of pain in patients with DIABETES MELLITUS and FIBROMYALGIA.
价 格：￥电议型 号：T1471产 地：中国大陆
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T1469Levocetirizine；左西替利嗪Levocetirizine HCl；Levocetirizine HCl|||左西替利嗪
Levocetirizine is a Histamine-1 Receptor Antagonist. The mechanism of action of levocetirizine is as a Histamine H1 Receptor Antagonist.
价 格：￥电议型 号：T1469产 地：中国大陆
