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T4196Betahistine EP Impurity C；化合物NSC19005NSC19005；NSC19005
Betahistine EP Impurity C (NSC19005) is structurally related to Betahistine. Betahistine EP Impurity C is a dimer of Betahistine.
价 格：￥电议型 号：T4196产 地：中国大陆
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T39900Thalidomide-O-amide-C5-NH2；Thalidomide-O-amide-C5-NH2Thalidomide-O-amide-C5-NH2；Thalidomide-O-amide-
Thalidomide-O-amide-C5-NH2 is a chemically synthesized conjugate, serving as an E3 ligase ligand-linker, which combines a cereblon ligand derived from Thalidomide with a linker that is commonly employed in PROTAC technology.
价 格：￥电议型 号：T39900产 地：中国大陆
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T39350Sebetralstat；化合物SebetralstatKVD900；KVD900
Sebetralstat (KVD900) is an inhibitor of plasma kallikrein and can be used in studies about metabolic diseases.
价 格：￥电议型 号：T39350产 地：中国大陆
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T39258PulrodemstatPulrodemstatLSD1-IN-7|||CC-90011
Pulrodemstat (CC-90011) is a highly potent and selective inhibitor of lysine specific demethylase-1 (LSD1). It exhibits a reversible mode of action and can be administered orally. With an impressive IC50 of 0.25 nM, Pulrodemstat effectively suppresses the enzymatic activity of LSD1. Notably, it demonstrates minimal inhibition against LSD2, MOA-A, and MAO-B enzymes. Moreover, Pulrodemstat possesses remarkable anticancer properties, promoting differentiation in acute myeloid leukemia (AML) and sma
价 格：￥电议型 号：T39258产 地：中国大陆
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T39009CAP18 (rabbit)；CAP18 (rabbit)CAP18 (rabbit)；CAP18 (rabbit)
CAP18 (rabbit) is a 37 amino acid antimicrobial peptide derived from rabbit granulocytes. It exhibits extensive antimicrobial activity against both Gram-positive (IC50, 130-200 nM) and Gram-negative (IC50, 20-100 nM) bacteria. Thus, CAP18 (rabbit) holds promise for the study and advancement of bacterial sepsis research.
价 格：￥电议型 号：T39009产 地：中国大陆
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T39008PRMT5-IN-4PRMT5-IN-4PRMT5-IN-4
PRMT5-IN-4 (compound AAA-1) is a PRMT5 inhibitor.
价 格：￥电议型 号：T39008产 地：中国大陆
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T390073,4-Dimethoxybenzamide；3,4-二甲氧基苯甲酰胺3,4-Dimethoxybenzamide
3,4-Dimethoxybenzamide, amide, is found in the solid culture of Streptoverticillium morookaense . 3,4-Dimethoxybenzamide can be used as the starting material to preparation Itopride hydrochloride.
价 格：￥电议型 号：T39007产 地：中国大陆
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T39006Bromo-PEG2-THP；Bromo-PEG2-THPBromo-PEG2-THP；Bromo-PEG2-THP
Bromo-PEG2-THP 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：T39006产 地：中国大陆
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T39005OVA (55-62)；OVA (55-62)OVA (55-62)
OVA 55-62 is a truncated peptide derived from the ovalbumin (OVA) antigen, specifically designed to bind to the H2-Kb mouse major histocompatibility complex (MHC) class I molecule.
价 格：￥电议型 号：T39005产 地：中国大陆
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T39002Azido-PEG1；Azido-PEG1Azido-PEG1；Azido-PEG1
Azido-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T39002产 地：中国大陆
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T39001FGFR-IN-1；FGFR-IN-1FGFR-IN-1
FGFR-IN-1 is a highly effective inhibitor targeting the Fibroblast Growth Factor Receptor (FGFR) group, comprising FGFR1, FGFR2, and FGFR3, with an impressive inhibitory concentration (IC 50) of less than 100 nM (US20130338134A1, example 219).
价 格：￥电议型 号：T39001产 地：中国大陆
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T39000Zaloglanstat；ZaloglanstatGRC-27864|||ISC-27864；GRC-27864|||ISC-27864
Zaloglanstat (ISC-27864) is a potent inhibitor of microsomal prostaglandin E synthase-1 (mPGES-1). It is utilized in the research of various conditions, including asthma, osteoarthritis, rheumatoid arthritis, acute or chronic pain, and neurodegenerative diseases.
价 格：￥电议型 号：T39000产 地：中国大陆
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T3900Emodin-8-glucoside；大黄素-8-β-D-吡喃葡萄糖苷Emodin glucoside B|||Anthraglycoside B；大黄素-8-β-D-吡喃葡萄糖苷|||Emodin
Emodin-8-glucoside (Anthraglycoside B) functions to protect from focal cerebral injury induced by ischemia and reperfusion. Emodin-8-beta-D-glucoside directly stimulates cell proliferation and differentiation of osteoblasts.
价 格：￥电议型 号：T3900产 地：中国大陆
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T38900Renin FRET Substrate I；Renin FRET Substrate IRenin FRET Substrate I
Renin FRET Substrate I is a specific compound that functions as a substrate for human renin. It is specifically designed to contain the exact cleavage site found in the N-terminal peptide of human angiotensinogen.
价 格：￥电议型 号：T38900产 地：中国大陆
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T38598CBK289001；CBK289001CBK289001
CBK289001 is a tartrate-resistant acid phosphatase (TRAP/ACP5) inhibitor. CBK289001 inhibits TRAP 5b MV , TRAP 5b OX and TRAP 5a OX with IC 50 s of 125 μM, 4.21 μM and 14.2 μM, respectively.
价 格：￥电议型 号：T38598产 地：中国大陆
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T37900UDP-Glucuronic Acid (sodium salt hydrate)；UDP-Glucuronic Acid (sodium salt hydrate)UDP-Glucuronic Ac
UDP-Glucuronic acid is a nucleoside diphosphate sugar that is a source of glucuronic acid for polysaccharide biosynthesis. This compound can be used for the formation of many glucuronides with various aglycones.1
价 格：￥电议型 号：T37900产 地：中国大陆
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T3700SCH900776 (S-isomer)；化合物SCH900776 S-isomerMK-8776 S-isomer|||SCH900776 S-isomer；MK-8776 S-isomer|||S
SCH900776 S-isomer (MK-8776 S-isomer) is an effective, specific and orally bioavailable inhibitor of checkpoint kinase Chk1 (IC50: 3 nM). It also inhibitors Chk2 (IC50: 1500 nM) and cyclin-dependent kinase CDK2 (IC50: 160 nM).
价 格：￥电议型 号：T3700产 地：中国大陆
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T36900PD-1/PD-L1-IN-NP19；化合物PD-1/PD-L1-IN-NP19PD-1/PD-L1-IN-NP19；PD-1/PD-L1-IN-NP19
PD-1/PD-L1-IN-NP19, a PD-1/PD-L1 inhibitor, exhibits an IC50 of 12.5 nM against the human PD-1/PD-L1 interaction, potentially activating the tumor immune microenvironment and contributing to its antitumor effects[1].
价 格：￥电议型 号：T36900产 地：中国大陆
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T3685SR9009；化合物SR9009Stenabolic|||REV-ERB Agonist II；Stenabolic|||REV-ERB Agonist II
SR9009 (Stenabolic), a REV-ERB agonist, increases the constitutive repression of genes regulated by REV-ERBα/ERBβ (IC50: 670/800 nM). Through activation of REV-ERB, SR9009 can decrease circadian locomotor activity during the dark phase and alter the expression pattern of core clock genes in the hypothalami of mice. The circadian pattern of expression of an array of metabolic genes in the liver, skeletal muscle, and adipose tissue was also altered in mice exposed to SR9009, resulting in increased
价 格：￥电议型 号：T3685产 地：中国大陆
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T36395Trotabresib；化合物TrotabresibCC-90010；CC-90010
Trotabresib (CC-90010) is an orally active inhibitor of BET and can be used in studies about advanced solid tumors.
价 格：￥电议型 号：T36395产 地：中国大陆
