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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
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T15683L-689502；化合物 T15683L-689502
L-689502 is a potent HIV-l protease inhibitor (IC50: 1 nM).
价 格：￥电议型 号：T15683产 地：中国大陆
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T15681L-161982；化合物L-161982L-161982
L-161982 is a selective antagonist of EP4 receptor. L-161982 could inhibit PGE2-induced ERK phosphorylation and cell proliferation of HCA-7 cells. L-161982 could alleviate collagen-induced arthritis in mice.
价 格：￥电议型 号：T15681产 地：中国大陆
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T15680L-159282；化合物 T15680MK 996；MK 996
L-159282 is an orally active and nonpeptide angiotensin II receptor antagonist. It also has anti-hypertensive activity.
价 格：￥电议型 号：T15680产 地：中国大陆
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T1568Amoxapine阿莫沙平阿莫沙平|||CL-67772
Amoxapine (CL-67772) exerts its antidepressant effect by inhibiting the re-uptake of norepinephrine and, to a lesser degree, of serotonin, at adrenergic nerve endings and blocks the response of dopamine receptors to dopamine. Amoxapine is a tricyclic antidepressant of the dibenzoxazepine class. This drug is used to treat symptoms of depression and may cause tardive dyskinesia. Amoxapine also binds to alpha-adrenergic, histaminergic, and cholinergic receptors which accounts for many of the side e
价 格：￥电议型 号：T1568产 地：中国大陆
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T15679L 152804；化合物L 152804L 152804
L 152804 is a specific antagonist of the neuropeptide Y Y5 receptor and modulates food intake and energy expenditure thus causing weight loss in diet-induced obese mice.
价 格：￥电议型 号：T15679产 地：中国大陆
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T15678KZR-504；化合物 T15678KZR-504
KZR-504 is a selective inhibitor of immunoproteasome low molecular mass polypeptide 2 (LMP2) (IC50s: 51 nM, 4.274 μM for LMP2 and LMP7, respectively).
价 格：￥电议型 号：T15678产 地：中国大陆
