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T15703Lactimidomycin；化合物 T15703Lactimidomycin
Lactimidomycin, isolated from Streptomyces, is an inhibitor of eukaryotic translation elongation. It is also a potent and non-toxic inhibitor of dengue virus 2 and other RNA viruses. Lactimidomycin has an antiproliferative effect on tumor cell lines. It inhibits protein synthesis (IC50: 37.82 nM).
价 格：￥电议型 号：T15703产 地：中国大陆
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T15702Lactacystin；蛋白酶体抑制剂Lactacystin
Lactacystin is an antibiotic Streptomyces spp. the metabolite and is an effective and selective proteasome inhibitor (IC50: 4.8 μM for 20S proteasome). Lactacystin inhibits cell growth and induces neurite outgrowth and also inhibits the lysosomal enzyme cathepsin A.
价 格：￥电议型 号：T15702产 地：中国大陆
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T15701Methyldopa hydrochloride；化合物 T15701L-(-)-α-Methyldopa hydrochloride|||MK-351 hydrochloride；L-(-)-α-M
L-(-)-α-Methyldopa hydrochloride is an alpha-adrenergic agonist psychoactive drug. It is used as a sympatholytic or antihypertensive. Methyldopa has a dual mechanism of action. It is a competitive inhibitor of the enzyme DOPA decarboxylase, which converts L-DOPA into dopamine.
价 格：￥电议型 号：T15701产 地：中国大陆
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T15700L-Xylose；L-(-)木糖L-(-)-Xylose；L-(-)-Xylose|||L-(-)木糖
L-Xylose (L-(-)-Xylose), a Xylose levo-isomer, is classified as the aldopentose type?monosaccharide.
价 格：￥电议型 号：T15700产 地：中国大陆
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T1570Telmisartan；替米沙坦BIBR 277；BIBR 277|||替米沙坦
Telmisartan (BIBR 277) is an Angiotensin 2 Receptor Blocker. The mechanism of action of telmisartan is as an Angiotensin 2 Receptor Antagonist.
价 格：￥电议型 号：T1570产 地：中国大陆
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T15699L-Thyroxine sodium salt pentahydrate；L-甲状腺素钠五水合物Sodium levothyroxine pentahydrate|||Levothyroxine；左旋
L-Thyroxine sodium salt pentahydrate, also known as Levothyroxine, is a synthetic hormone utilized in the study of hypothyroidism. It is biologically activated into Triiodothyronine (T3) from its original form, L-Thyroxine (T4), through conversion by DIO enzymes.
价 格：￥电议型 号：T15699产 地：中国大陆
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T15698L-Palmitoylcarnitine；棕榈酰肉碱L-Palmitoylcarnitine
L-Palmitoylcarnitine is a metabolite of fatty acid.
价 格：￥电议型 号：T15698产 地：中国大陆
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T15697L-NMMA acetate；化合物L-NMMA acetateTilarginine acetate|||Methylarginine acetate；Tilarginine acetate|||M
L-NMMA acetate (Tilarginine acetate) is an inhibitor of nitric oxide synthase of all NOS isoforms (i.e. NOS1, NOS2, and NOS3). The Ki values are 0.18, 0.4, and 6 ?M for nNOS, eNOS, and iNOS, respectively.
价 格：￥电议型 号：T15697产 地：中国大陆
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T15696NEP-IN-2；化合物 T15696NEP-IN-2
NEP-IN-2 is an inhibitor of neutral endopeptidase. It also is used in the research of proliferation in atherosclerosis, restenosis.
价 格：￥电议型 号：T15696产 地：中国大陆
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T15695L-Lysine thioctate；化合物 T15695L-Lysine thioctate
L-Lysine thioctate is a lipoamidase substrate.
价 格：￥电议型 号：T15695产 地：中国大陆
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T15694L-Homopropargylglycine；化合物 T15694L-Homopropargylglycine
L-Homopropargylglycine is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1].
价 格：￥电议型 号：T15694产 地：中国大陆
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T15693L-Azidohomoalanine；化合物 T15693L-Azidohomoalanine
L-Azidohomoalanine, an alkyl chain-derived PROTAC linker, is utilized in the synthesis of PROTACs[1].
价 格：￥电议型 号：T15693产 地：中国大陆
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T15692L-AP4；化合物 T15692L-APB|||L-AP 4；L-APB|||L-AP 4
L-APB is an effective and specific agonist for the group III mGluRs (EC50s: 0.13, 0.29, 1.0, 249 μM for mGlu4, mGlu8, mGlu6, and mGlu7 receptors, respectively).
价 格：￥电议型 号：T15692产 地：中国大陆
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T15690L-902688；化合物 T15690L-902688
L-902688 is an orally active EP4 receptor agonist (Ki: 0.38 nM; EC50: 0.6 nM). L-902688 displays >4,000-fold selective for EP4 over other EP and prostanoid receptors.
价 格：￥电议型 号：T15690产 地：中国大陆
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T1569Tigecycline；替加环素GAR-936；替加环素|||GAR-936
Tigecycline (GAR-936) is a broad-spectrum glycylcycline antibiotic derived from tetracycline. Tigecycline binds to the 30S ribosomal subunit, thereby interfering with the binding of aminoacyl-tRNA to the mRNA-ribosome complex.
价 格：￥电议型 号：T1569产 地：中国大陆
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T15689L-798106化合物 T15689CM9|||GW671021
L-798106 is a highly selective prostanoid EP3 receptor antagonist (Ki=0.3 nM). It also has micromolar activities at EP4, EP1, and EP2 receptors (Ki: 916 nM, >5000 nM, and >5000 nM at EP4, EP1, and EP2, respectively).
价 格：￥电议型 号：T15689产 地：中国大陆
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T15688L-771688；化合物L-771688SNAP 6383；SNAP 6383
L-771688 (SNAP 6383) is a novel potent and selective α1A-adrenoceptor antagonist with a Ki value of 0.43±0.02 nM.L-771688 KE is used for the treatment of benign prostatic hyperplasia.
价 格：￥电议型 号：T15688产 地：中国大陆
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T15687Thioflosulide；化合物ThioflosulideL-745337；L-745337
Thioflosulide (L-745337) is a selective and potent COX2 inhibitor (IC50: 2.3 nM) with anti-inflammatory activity for the study of gastric ulcers.
价 格：￥电议型 号：T15687产 地：中国大陆
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T15686L-741626；化合物L-7416263-(4-(4-Chlorophenyl-4-hydroxypiperidino)methyl)indole；3-(4-(4-Chlorophenyl-4-hy
L-741626 (3-(4-(4-Chlorophenyl-4-hydroxypiperidino)methyl)indole) is a selective antagonist of D2 dopamine receptor (Ki: 2.4, 100, and 220 nM for human D2, D3 and D4 receptors respectively).
价 格：￥电议型 号：T15686产 地：中国大陆
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T15684L-689560；化合物L-689560L-689560
L-689560 is widely used as a radiolabeled ligand in binding studies and used to study the roles of NMDA receptors in normal neurological processes as well as in diseases. At the GluN1 glycine binding site, L-689560 is an effective N-methyl-D-aspartate (NMDA) receptor antagonist.
价 格：￥电议型 号：T15684产 地：中国大陆
