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T18793Tetrazine-PEG5-SS-amine；化合物 T18793Tetrazine-PEG5-SS-amine
Tetrazine-PEG5-SS-amine is a cleavable 5-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T18793产 地：中国大陆
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T18792Tetrazine-PEG4-SS-Py；化合物 T18792Tetrazine-PEG4-SS-Py
Tetrazine-PEG4-SS-Py is a cleavable PEG ADC linker comprising four units. It is specifically designed for the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T18792产 地：中国大陆
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T18791Tetrazine-PEG4-SS-NHS；化合物 T18791Tetrazine-PEG4-SS-NHS
Tetrazine-PEG4-SS-NHS is a cleavable four-unit polyethylene glycol (PEG) linker employed for the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T18791产 地：中国大陆
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T18790Tetrazine-PEG4-oxyamine hydrochloride；化合物 T18790Tetrazine-PEG4-oxyamine hydrochloride
Tetrazine-PEG4-oxyamine (hydrochloride) is a cleavable 4-unit polyethylene glycol (PEG) linker, employed for the synthesis of antibody-drug conjugates (ADCs) [1].
价 格：￥电议型 号：T18790产 地：中国大陆
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T18793-Methyladenine；3-甲基腺嘌呤3-MA|||NSC 66389；3-MA|||3-甲基腺嘌呤|||NSC 66389
3-Methyladenine (3-MA) is a PI3K inhibitor that selectively inhibits class IB PI3Kγ (IC50=60 μM) and class III VPS34 (IC50=25 μM). 3-Methyladenine inhibits autophagy.
价 格：￥电议型 号：T1879产 地：中国大陆
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T17879E3 ligase Ligand 8；化合物E3 ligase Ligand 8E3 ligase Ligand 8
E3 ligase Ligand 8 is a ligand for E3 ubiquitin ligase. The E3 ligase Ligand 8 can be linked to protein ligands through linkers to form PROTACs, which are inducers of ubiquitination-mediated degradation of cancer-promoting proteins.
价 格：￥电议型 号：T17879产 地：中国大陆
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T16879LSHU 9119 acetate；化合物SHU 9119 acetateSHU 9119 acetate (168482-23-3 free base)；SHU 9119 acetate (16848
SHU 9119 acetate is a well-known antagonist of human melanocortin 3 and 4 (hMC3R, hMC4R) receptors and a partial hMC5R agonist. The IC50 values of human MC3R, MC4R and MC5R is 0.23, 0.06, and 0.09 nM respectively.
价 格：￥电议型 号：T16879L产 地：中国大陆
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T16879SHU 9119；化合物 T16879SHU 9119
SHU 9119 is an effective human melanocortin 3 and 4 receptors (MC3/4R) antagonist and a partial MC5R agonist (IC50: 0.23, 0.06, and 0.09 nM for human MC3R, MC4R and MC5R, respectively).
价 格：￥电议型 号：T16879产 地：中国大陆
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T15879m-PEG4-Hydrazide；化合物 T15879m-PEG4-Hydrazide
m-PEG4-Hydrazide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15879产 地：中国大陆
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T15439GSK3395879；化合物 T15439GSK3395879
GSK3395879 is a selective and orally bioavailable antagonist of transient receptor potential vanilloid-4 (TRPV4) (IC50: 1 nM for hTRPV4).
价 格：￥电议型 号：T15439产 地：中国大陆
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T14879CB 300919；化合物 T14879CB 300919
CB 300919 is a quinazoline-based antitumor agent with high activity in the CH1 human ovarian tumor xenograft and has continuous exposure (96 h) growth inhibition (IC50: 2 nM).
价 格：￥电议型 号：T14879产 地：中国大陆
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T14384AZD8797；化合物KAND567KAN-0440567|||KAND567；KAN-0440567|||KAND567
AZD8797 (KAND567) is an orally available, selective and potent human CX3CR1-converting antagonist with inhibitory effects on CX3CR1 and CXCR2, and potentially protects against SARS-CoV-2-induced neuronal damage, preventing worsening of nociceptive sensitization and microglial activation in a migraine model of rats following seizures.
价 格：￥电议型 号：T14384产 地：中国大陆
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T13879(S)-Verapamil hydrochloride；化合物 T13879(S)-(-)-Verapamil hydrochloride；(S)-(-)-Verapamil hydrochlorid
(S)-Verapamil hydrochloride is an inhibitor of leukotriene C4 (LTC4) and calcein transport by MRP1,and leads to the death of potentially resistant tumor cells.
价 格：￥电议型 号：T13879产 地：中国大陆
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T13372YM-58790 hydrochloride；化合物 T13372YM-58790 hydrochloride
YM-58790 hydrochloride is a potent M3 muscarinic receptor antagonist(Ki of 15 nM).
价 格：￥电议型 号：T13372产 地：中国大陆
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T130879Altamisic acid；化合物 Altamisic acidAltamisic acid
Altamisic acid is a useful organic compound for research related to life sciences and the catalog number is T130879.
价 格：￥电议型 号：T130879产 地：中国大陆
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T12879Sematilide；化合物 T12879CK-1752；CK-1752
Sematilide is a blocker of selective IKr channel.
价 格：￥电议型 号：T12879产 地：中国大陆
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T124879Eupomatenoid 12；化合物 Eupomatenoid 12Eupomatenoid 12
Eupomatenoid 12 is a useful organic compound for research related to life sciences. The catalog number is T124879 and the CAS number is 41365-37-1.
价 格：￥电议型 号：T124879产 地：中国大陆
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T11879LS-102；化合物 T11879LS-102
LS-102, a selective E3 ubiquitin ligase synoviolin (Syvn1) inhibitor, effectively inhibits the autoubiquitination of synoviolin, exhibiting an IC50 value of 35 μM. This compound shows promise for the treatment of rheumatoid arthritis.
价 格：￥电议型 号：T11879产 地：中国大陆
