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T4087S 38093 HCl；化合物S 38093 HClS 38093 HCl
S 38093 is a novel brain-penetrant antagonist/inverse agonist of H3 receptors.
价 格：￥电议型 号：T4087产 地：中国大陆
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T4080Leonurine hydrochloride；盐酸益母草碱SCM-198 hydrochloride|||SCM-198 HCl；盐酸益母草碱|||SCM-198 hydrochloride|||S
Leonurine hydrochloride (SCM-198 hydrochloride) , a major alkaloid compound extracted from Leonurus japonicas Houtt. (Labiatae), is considered to have antitumor roles.
价 格：￥电议型 号：T4080产 地：中国大陆
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T4074LGSK872 HCl（1346546-69-7 free base）；化合物GSK872 HClGSK2399872A；GSK2399872A
GSK872 HCl（1346546-69-7 free base） (GSK2399872A) is an effective and specific RIP3 kinase inhibitor. It binds RIP3 kinase domain with high affinity (IC50: 1.8 nM) and inhibits kinase activity (IC50: 1.3 nM).
价 格：￥电议型 号：T4074L产 地：中国大陆
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T40594iHCK-37；iHCK-37iHCK-37|||ASN05260065；iHCK-37|||ASN05260065
iHCK-37 (ASN05260065) is a high-potency, selective inhibitor of Hck with a Ki value of 0.22 μM. It effectively inhibits HIV-1 viral replication, exhibiting an EC50 value of 12.9 μM. Primarily employed in chronic myeloid leukemia (CML) research, iHCK-37 demonstrates promising potential for studying and understanding this disease.
价 格：￥电议型 号：T40594产 地：中国大陆
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T4047LBisantrene HCl化合物 T4047LCL216942|||CL-216942|||NSC-337766|||CL 216942
Bisantrene (CL-216942; NSC 337766) is a topoisomerase II poison and DNA intercalator. It can be used as a Rac1 inhibitor or model compound to study P-glycoprotein-mediated multi-drug resistance (MDR1). Bisantrene inserts and disrupts the configuration of DNA, leading to DNA single-strand breaks, DNA-protein cross-links, and DNA replication inhibition.
价 格：￥电议型 号：T4047L产 地：中国大陆
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T40405CH2COOH-PEG3-CH2COOHCH2COOH-PEG3-CH2COOHCH2COOH-PEG3-CH2COOH
CH2COOH-PEG3-CH2COOH 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：T40405产 地：中国大陆
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T4023L-Argininamide dihydrochloride；L-精氨酰胺二盐酸盐H-Arg-NH2.2HCl；L-精氨酰胺二盐酸盐|||H-Arg-NH2.2HCl
L-Argininamide dihydrochloride (H-Arg-NH2.2HCl) is used as a model compound in studies of the physicochemical characteristic of ligand binding DNA aptamers and their potential development as fluorescent aptasensors.
价 格：￥电议型 号：T4023产 地：中国大陆
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T4013SGC2085 HCl；化合物SGC2085 HClSGC2085 HCl
SGC2085 is a potent and selective coactivator associated arginine methyltransferase 1 (CARM1) Inhibitor with an IC50 of 50 nM and more than undred-fold selectivity over other PRMTs. CARM1 is an important positive modulator of Wnt/β-catenin transcription and neoplastic transformation in colorectal cancer as well as a critical factor in estrogen-stimulated breast cancer growth, and its depletion results in decreased proliferation of myeloid leukemia cells in vivo.
价 格：￥电议型 号：T4013产 地：中国大陆
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T40049MC-AAA-NHCH2OCH2COO-7-aminomethyl-10-methyl-11-fluoro camptothecin；MC-AAA-NHCH2OCH2COO-7-aminomethyl
MC-AAA-NHCH2OCH2COO-7-aminomethyl-10-methyl-11-fluoro camptothecin (compound 21a), is a camptothecin payload which can be utilized in the synthesis of a camptothecin antibody-drug conjugate (ADC) by conjugation to a monoclonal antibody (mAb).
价 格：￥电议型 号：T40049产 地：中国大陆
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T40048MC-AAA-NHCH2OCH2COOH；MC-AAA-NHCH2OCH2COOHMC-AAA-NHCH2OCH2COOH；MC-AAA-NHCH2OCH2COOH
MC-AAA-NHCH2OCH2COOH (compound 20) is a cleavable antibody-drug conjugate (ADC) linker. Its primary application lies in the synthesis of ADCs.
价 格：￥电议型 号：T40048产 地：中国大陆
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T3999D(+)-Galactosamine hydrochlorideD-氨基半乳糖盐酸盐D-半乳糖胺盐酸盐|||D-氨基半乳糖盐酸盐|||D-Galactosamine HCl
D(+)-Galactosamine hydrochloride (D-Galactosamine HCl) hepatotoxicity is associated with endotoxin sensitivity and mediated by lymphoreticular cells in mice.
价 格：￥电议型 号：T3999产 地：中国大陆
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T39775CH2COOH-PEG9-CH2COOH；CH2COOH-PEG9-CH2COOHCH2COOH-PEG9-CH2COOH；CH2COOH-PEG9-CH2COOH
CH2COOH-PEG9-CH2COOH 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：T39775产 地：中国大陆
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T3938H-HomoArg-OH.HCl；L-高精氨酸盐酸盐NSC 145416|||L-Homoarginine hydrochloride|||L(+)-Homoarginine hydrochlorid
H-HomoArg-OH.HCl (L-Homoarginine hydrochloride) is a specific inhibitor of liver-type alkaline phosphatase.
价 格：￥电议型 号：T3938产 地：中国大陆
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T39284EST73502 HCl；化合物EST73502 HClEST73502 HCl
EST73502 is an agonist of μ-opioid receptor(Ki = 64 nM) agonist and an antagonist of σ1 receptor (Ki = 118 nM). EST73502 displays antinociceptive activity.
价 格：￥电议型 号：T39284产 地：中国大陆
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T39252LAnticonvulsant agent 10 HCl；Anticonvulsant agent 10 盐酸盐Anticonvulsant agent 10 HCl
5-[(1S,2S)-2-[(Cyclopropylmethyl)amino]cyclopropyl]-N-(tetrahydro-2H-pyran-4-yl)thiophene-3-carboxamide hydrochloride is a cyclopropanoid enzyme compound that acts as a lysine-specific demethylase-1 inhibitor for schizophrenia, developmental disorders, and neurodegenerative diseases.
价 格：￥电议型 号：T39252L产 地：中国大陆
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T39186Boc-NHCH2CH2-PEG1-azide；Boc-NHCH2CH2-PEG1-azideBoc-NHCH2CH2-PEG1-azide；Boc-NHCH2CH2-PEG1-azide
Boc-NHCH2CH2-PEG1-azide 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：T39186产 地：中国大陆
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T38960LQL-X-138 HCl；QL-X-138 盐酸盐QL-X-138 HCl（1469988-63-3 Free base）；QL-X-138 HCl（1469988-63-3 Free base）
QL-X-138 HCl is a novel selective and highly potent BTK/MNK dual-kinase inhibitor with anticancer activity that binds covalently to BTK and noncovalently to MNK. QL-X-138 HCl inhibited BTK, MNK1, and MNK2 kinases. QL-X-138 HCl has anti-dengue virus 2 activity and shows anti-proliferative activity in acute myeloid leukemia cells. QL-X-138 HCl can be used to study lymphoma and leukemia.
价 格：￥电议型 号：T38960L产 地：中国大陆
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T38698Cathayanon H；Cathayanon HCathayanon H
Cathayanon H, a compound derived from the paper mulberry tree, exhibits cytotoxicity against human ovarian carcinoma cells.
价 格：￥电议型 号：T38698产 地：中国大陆
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T38234HCoV-229E-IN-1；HCoV-229E-IN-1HCoV-229E-IN-1
HCoV-229E-IN-1 is a potent inhibitor of HCoV-229E replication, demonstrating efficacy with an EC50 value of 0.65 μM in MTS cells and 0.6 μM in CPE cells[1].
价 格：￥电议型 号：T38234产 地：中国大陆
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T38079DL-Propargylglycine HCl；DL-炔丙基甘氨酸盐酸盐DL-Propargyl Glycine HCl|||DL-Propargyl Glycine hydrochloride；DL
DL-Propargylglycine HCl (DL-Propargyl Glycine HCl) is a potent irreversible inhibitor of cystathionine γ-cleaving enzyme and can be used in the study of heart failure.
价 格：￥电议型 号：T38079产 地：中国大陆
