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T358404-Amino-6-chloro-1,3-benzenedisulfonamide；4-Amino-6-chloro-1,3-benzenedisulfonamide4-Amino-6-chloro-
4-Amino-6-chloro-1,3-benzenedisulfonamide is a carbonic anhydrase inhibitor.1 Formulations containing this compound are diuretics.2 4-Amino-6-chloro-1,3-benzenedisulfonamide is detected as a hydrolysis product of chlorothiazide in the urine.2 Diuretics, including chlorothiazide, have been abused as performance-enhancing drugs and masking agents in sports doping.3
价 格：￥电议型 号：T35840产 地：中国大陆
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T358393-Iodothyronamine (hydrochloride)；3-Iodothyronamine (hydrochloride)3-Iodothyronamine (hydrochloride)
3-Iodothyronamine is derived from the deiodination and decarboxylation of endogenous thyroxine. It activates the G protein-coupled receptor known as trace amine-associated receptor 1 at nanomolar concentrations whereupon it rapidly influences thyroid hormone actions including body temperature, heart rate, and cardiac output. It has also been reported to function in controlling lipid and glucose utilization, hormonal secretion, and neuronal function, and has been considered for use in chemically-
价 格：￥电议型 号：T35839产 地：中国大陆
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T35838GSK3182571；GSK3182571GSK3182571
GSK3182571 is a non-speci c kinase inhibitor[1].
价 格：￥电议型 号：T35838产 地：中国大陆
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T35837Flufenoxuron；氟虫脲Flufenoxuron
Flufenoxuron, a benzoylurea insecticide, acts as a chitin synthesis inhibitor. Its usage involves inhibiting chitin synthesis, reducing molting, and impeding egg hatching, resulting in the prevention of insect development[1].
价 格：￥电议型 号：T35837产 地：中国大陆
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T35836PMX-205 (trifluoroacetate salt)；PMX-205 (trifluoroacetate salt)PMX-205 (trifluoroacetate salt)
PMX-205 is a cyclic hexapeptide that acts as a potent antagonist of C5a receptor (C5aR; IC50= 31 nM).1It is orally active and blocks inflammatory signaling and symptoms in animal models of colitis and allergic asthma.2,3PMX-205 is also brain penetrant and reduces neuroinflammation and neurodegeneration in an animal model of Alzheimer´s disease.4
价 格：￥电议型 号：T35836产 地：中国大陆
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T35835FFN-102 (trifluoroacetate salt)；FFN-102 (trifluoroacetate salt)FFN-102 (trifluoroacetate salt)
FFN-102 (trifluoroacetate salt) is a synthetic biogenic neurotransmitter analog with pH-dependent fluorescence and electroactivity.
价 格：￥电议型 号：T35835产 地：中国大陆
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T35834L(Sar?)-Angiotensin II acetate；化合物(Sar?)-Angiotensin II acetate(Sar?)-Angiotensin II acetate
(Sar?)-Angiotensin II acetate, an analogue of Angiotensin II, is a specific agonist of angiotensin AT1 receptor. It binds to brain membrane-rich particles, with a Kd of 2.7 nM. It can stimulate protein synthesis and cell growth in embryonic chick myocytes.
价 格：￥电议型 号：T35834L产 地：中国大陆
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T35834(Sar1)-Angiotensin II；(Sar?)-Angiotensin II(Sar?)-Angiotensin II；(Sar?)-Angiotensin II
The substitution with Sar at position 1 of angiotensin II resulted in a partial agonistic activity.
价 格：￥电议型 号：T35834产 地：中国大陆
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T35833(S)-(-)-Atenolol；(S)-(-)-阿替洛尔(S)-(-)-Atenolol
(S)-(-)-Atenolol has beta-adrenergic blocking effects.
价 格：￥电议型 号：T35833产 地：中国大陆
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T35832Brain Natriuretic Peptide (1-32), rat acetate；Brain Natriuretic Peptide (1-32), rat acetateBrain Nat
Brain Natriuretic Peptide (1-32), rat acetate (BNP (1-32), rat acetate) is a 32 amino acid polypeptide hormone synthesized by ventricular cardiomyocytes as a result of myocardial cell stretching (cardiomyocyte distension)[1].
价 格：￥电议型 号：T35832产 地：中国大陆
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T35831Deoxy Donepezil (hydrochloride)；Deoxy Donepezil (hydrochloride)Deoxy Donepezil (hydrochloride)
Deoxy donepezil is a potential impurity found in bulk preparations of the acetylcholinesterase inhibitor donepezil .1It is produced as a by-product during donepezil synthesis.2
价 格：￥电议型 号：T35831产 地：中国大陆
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T35830Dehydro Olmesartan；Dehydro OlmesartanDehydro Olmesartan
Dehydro Olmesartan, deriving from Olmesartan, acts as an angiotensin II receptor (AT1R) antagonist and exhibits potential for the study of high blood pressure [1][2].
价 格：￥电议型 号：T35830产 地：中国大陆
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T3583Macozinone；化合物PBTZ169PBTZ169；PBTZ169
Macozinone (PBTZ169) inhibits decaprenylphosphoryl-β-d-ribose 2′-oxidase (DprE1), more efficiently than BTZ043.
价 格：￥电议型 号：T3583产 地：中国大陆
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T35829CC-90005；CC-90005CC-90005
CC-90005 is a potent, selective and orally active inhibitor of protein kinase C-θ (PKC-θ), with an IC50 of 8 nM. CC-90005 shows selectivity for PKC-θ over PKC-δ (IC50=4440 nM). CC-90005 can inhibit T cell activation by IL-2 expression[1].
价 格：￥电议型 号：T35829产 地：中国大陆
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T35828SR 3677 dihydrochlorideSR 3677 dihydrochlorideSR 3677 dihydrochloride
Potent and selective Rho-kinase inhibitor (IC50 values are 3 and 56 nM for ROCK-II and ROCK-I respectively).
价 格：￥电议型 号：T35828产 地：中国大陆
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T35827LPKCε Inhibitor Peptide acetate；化合物PKCε Inhibitor Peptide acetatePKCε Inhibitor Peptide acetate(18268
PKCε Inhibitor Peptide acetate is a selective PKCε inhibitor containing the site for its specific receptor for activated C kinase (RACK). PKCε Inhibitor Peptide acetate inhibits the translocation of PKCε, but not α-, β-, and δPKC.
价 格：￥电议型 号：T35827L产 地：中国大陆
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T35827Epsilon-V1-2；PKCε Inhibitor PeptidePKCε Inhibitor Peptide|||Protein Kinase C? Inhibitor Peptide|||?V
Protein kinase C (PKC ) is a calcium-independent, phospholipid- and diacylglycerol-dependent serine/threonine kinase involved in diverse signaling pathways, including those involved in neuronal signaling, cytoskeletal function, and inflammation.[1] PKC inhibitor peptide is a synthetic peptide corresponding to an amino acid sequence found in the amino terminal C2 domain of most mammalian forms of PKC .[2] It selectively and reversibly inhibits the translocation of PKC to intracellular membrane
价 格：￥电议型 号：T35827产 地：中国大陆
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T35826PKC fragment (530-558)；PKC fragment (530-558)PKC fragment (530-558)
PKC fragment (530-558) is a peptide fragment of protein kinase C (PKC) and is a potent PKC activator. Protein Kinase C (530-558) significantly inhibits osteoclastic bone resorption.
价 格：￥电议型 号：T35826产 地：中国大陆
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T35825Trichostatin C；Trichostatin CTrichostatin C
Trichostatin C is a glycosylated derivative of trichostatin A , the antifungal antibiotic that reversibly inhibits histone deacetylase. Trichostatin C is reported to be the first example of a glucopyranosyl hydroxamate identified in nature. It has been shown to induce the differentiation of a mouse erythroleukemia cell line and to increase histone H4 acetylation in B cells, though at higher concentrations than trichostatin A.
价 格：￥电议型 号：T35825产 地：中国大陆
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T35824Trapoxin A；Trapoxin ATrapoxin A
Trapoxin A is a microbial cyclic tetrapeptide that is an irreversible inhibitor of class I histone deacetylases (HDACs).
价 格：￥电议型 号：T35824产 地：中国大陆
