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T15582inS3-54A18
inS3-54A18 is an effective inhibitor of STAT3. inS3-54A18 has anticancer effects.
价 格：￥电议型 号：T15582产 地：中国大陆
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T14378LAZD5582 acetate (1258392-53-8 free base)
AZD5582 acetate is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis.
价 格：￥电议型 号：T14378L产 地：中国大陆
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T14378AZD5582AZD5582
AZD5582 is an antagonist of the inhibitor of apoptosis proteins (IAPs). Which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis[1].
价 格：￥电议型 号：T14378产 地：美洲
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T15582inS3-54A18inS3-54A18
inS3-54A18 is a potent inhibitor of STAT3. It has anti-cancer properties.
价 格：￥电议型 号：T15582产 地：美洲
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T75582Naja Melanoleuca Venom；化合物 Naja Melanoleuca VenomNaja Melanoleuca Venom
Naja Melanoleuca Venom (Forest Cobra Venom) is a snake venom derived from Naja Melanoleuca, exhibiting hemolytic activity against human erythrocytes. It contains α-neurotoxins that isolate from the venom and inhibit the GABAA receptor [1] [2].
价 格：￥电议型 号：T75582产 地：中国大陆
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T69488CB5255829；化合物 CB5255829CB5255829
CB5255829 is a novel inhibitor of Mycobacterium marinum MelF (Rv1936), exhibiting bacteriostatic/bactericidal activity against M. marinum and M. tuberculosis in vitro.
价 格：￥电议型 号：T69488产 地：中国大陆
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T655821-(4-Aminophenyl)-4-(4-hydroxyphenyl)piperazine；化合物 1-(4-Aminophenyl)-4-(4-hydroxyphenyl)piperazine1
1-(4-Aminophenyl)-4-(4-hydroxyphenyl)piperazine is a useful organic compound for research related to life sciences. The catalog number is T65582 and the CAS number is 74853-08-0.
价 格：￥电议型 号：T65582产 地：中国大陆
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T36201LAZD5582 TFA；AZD5582 三氟乙酸盐AZD5582 TFA（1258392-53-8 free base）；AZD5582 TFA（1258392-53-8 free ba
AZD5582 TFA is a potent IAP antagonist that binds to the BIR3 domain of cIAP1, cIAP2, and XIAP with IC50 values of 15, 21, and 15 nM, respectively.AZD5582 TFA induces apoptosis.
价 格：￥电议型 号：T36201L产 地：中国大陆
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T36201AZD5582 dihydrochloride；AZD 5582 dihydrochlorideAZD 5582 dihydrochloride；AZD 5582 dihydrochloride
Dimeric Smac mimetic; potent inhibitor of X-linked (XIAP) and cellular (cIAP) inhibitor of apoptosis protein (IC50 values are 15, 15 and 21 nM for XIAP, cIAP1 and cIAP2 respectively). Binds to the BIR3 domain of XIAP to prevent interaction with caspase-9. Causes degradation of cIAP1 and cIAP2 and induces apoptosis in MDA-MB-231 breast cancer cells. Causes tumor regression in MDA-MB-231 xenograft-bearing mice.
价 格：￥电议型 号：T36201产 地：中国大陆
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T35582H-Arg-Gly-Asp-Cys-OH (trifluoroacetate salt)；H-Arg-Gly-Asp-Cys-OH (trifluoroacetate salt)H-Arg-Gly-A
H-Arg-Gly-Asp-Cys-OH is a tetrapeptide that contains the arginine-glycine-aspartate (RGD) motif, a sequence that acts as a recognition site for various adhesion proteins.1It inhibits the binding of fibrinogen to endothelial cells and ADP-stimulated platelets with IC50values of 320 and 35 μM, respectively.2Implantation of titanium rods coated with H-Arg-Gly-Asp-Cys-OH increases bone formation in rat femurs.3H-Arg-Gly-Asp-Cys-OH has been conjugated to polyethylenimine to improve gene transfection
价 格：￥电议型 号：T35582产 地：中国大陆
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T30545BMS-955829；化合物 T30545BMS955829|||BMS 955829；BMS955829|||BMS 955829
BMS-955829 is a positive allosteric modulator (PAM).
价 格：￥电议型 号：T30545产 地：中国大陆
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T27934LY255582；化合物LY255582LY-255582|||LY 255582；LY-255582|||LY 255582
LY255582 is a selective centrally active opioid receptor antagonist with high affinity for mu, delta and kappa receptors with Ki of 0.4 nM, 5.2, 2.0 nM, respectively. LY255582 inhibits diet-associated increases in mesolimbic dopamine levels and reduces consumption of food intake. LY255582 is commonly used in obesity research. LY255582 is a potential compound for the study of opioid receptor-mediated cell signaling.
价 格：￥电议型 号：T27934产 地：中国大陆
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T25582Kinamycin C；化合物 T25582Kinamycin-C|||KinamycinC；Kinamycin-C|||KinamycinC
Kinamycin C is a bacterial metabolite used as an anticancer agent.
价 格：￥电议型 号：T25582产 地：中国大陆
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T15582inS3-54A18；化合物inS3-54A18inS3-54A18
inS3-54A18 is an effective inhibitor of STAT3. inS3-54A18 has anticancer effects.
价 格：￥电议型 号：T15582产 地：中国大陆
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T14378LAZD5582 acetate (1258392-53-8 free base)；化合物AZD5582 acetateAZD5582 acetate (1258392-53-8 free base)
AZD5582 acetate is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis.
价 格：￥电议型 号：T14378L产 地：中国大陆
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T14378AZD5582；化合物AZD5582AZD5582
AZD5582 is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. It induces apoptosis.
价 格：￥电议型 号：T14378产 地：中国大陆
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T125582Combreglucoside；化合物 CombreglucosideCombreglucoside
Combreglucoside is a useful organic compound for research related to life sciences. The catalog number is T125582 and the CAS number is 173485-48-8.
价 格：￥电议型 号：T125582产 地：中国大陆
