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T10893CS-722 Free base；化合物CS-722 Free baseCS-722 Free base
CS-722 Free base is a synthetic central muscle relaxant with muscle relaxant activity and inhibitory effect on spinal reflex. CS-722 Free base may inhibit spontaneous inhibitory post-synaptic current and excitatory post-synaptic current in hippocampal culture by inhibiting sodium current and calcium current.
价 格：￥电议型 号：T10893产 地：中国大陆
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T10892CS-003 Free base；化合物 T10892CS-003 Free base
CS-003 free base (CS-003) is a triple tachykinin receptor antagonist with high affinity for human (neurokinin) NK1, NK2 and NK3 receptors, with Ki values of 2.3 nM and 0.54 nM, respectively And 0.74 nM. CS-003 free base (CS-003) has therapeutic effects on neurokinin-related respiratory diseases.
价 格：￥电议型 号：T10892产 地：中国大陆
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T10884CRAC intermediate 1化合物CRAC intermediate 15-(S)-Fluorowillardiine
CRAC intermediate 1 (5-(S)-Fluorowillardiine) is a key intermediate in the chemical synthesis of a series of CRAC channel inhibitors.
价 格：￥电议型 号：T10884产 地：中国大陆
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T10883LCRA-026440 hydrochloride；化合物CRA-026440盐酸盐CRA-026440 hydrochloride（847460-34-8 Free base）；CRA-026440
CRA-026440 hydrochloride is a potent and broad-spectrum HDAC inhibitor. CRA-026440 hydrochloride exhibits Ki values against recombinant HDAC isoenzymes HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, and HDAC10 are 4 nM, 14 nM, 11 nM, 15 nM, 7 nM, and 20 nM, respectively. CRA-026440 hydrochloride exhibits antitumor and antiangiogenic activities.
价 格：￥电议型 号：T10883L产 地：中国大陆
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T10878CPFX2090；化合物 T10878CPFX2090
CPFX2090, a cephalosporin antibacterial compound.
价 格：￥电议型 号：T10878产 地：中国大陆
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T10865LCot inhibitor-1 hydrochloride；化合物Cot inhibitor-1盐酸盐Cot inhibitor-1 hydrochloride(915365-57-0 Free ba
Cot inhibitor-1 hydrochloride is an inhibitor of tumor progression loci-2 kinase (IC50 = 28 nM) and inhibits the production of TNF-α in human whole blood (IC50 = 5.7 nM).
价 格：￥电议型 号：T10865L产 地：中国大陆
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T1086Vitamin D2；维生素D2Calciferol|||Ergocalciferol|||Ercalciol；Calciferol|||Ergocalciferol|||Ercalciol|||维生
Ergocalciferol (Vitamin D2 (Calciferol)) is a derivative of ergosterol formed by ultraviolet rays breaking of the C9-C10 bond with a strong inhibitory effect against bladder tumor promotion by sodium saccharin, and it induces cell differentiation in leukemia cells. Vitamin D2 is an inhibitor of DNA Polymerase.
价 格：￥电议型 号：T1086产 地：中国大陆
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T10859COH34；化合物COH341-[(E)-(4-methylphenyl)sulfanyliminomethyl]naphthalen-2-ol；1-[(E)-(4-methylphenyl)sulf
COH34 (1-[(E)-(4-methylphenyl)sulfanyliminomethyl]naphthalen-2-ol) is a selective inhibitor of PARG with an IC50 of 0.37 nM and a Kd of 0.547 μM. COH34 prolongs PARylation at DNA lesions and traps DNA repair factors.
价 格：￥电议型 号：T10859产 地：中国大陆
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T10840CM-579 trihydrochloride (1846570-40-8 free base)；化合物 T10840CM-579 trihydrochloride；CM-579 trihydroch
CM-579 trihydrochloride is a first-in-class reversible and dual inhibitor of G9a and DNMT (IC50s: 16 nM, 32 nM) with potent in vitro cellular activity in a wide range of cancer cells.
价 格：￥电议型 号：T10840产 地：中国大陆
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T1084Apramycin sulfate；硫酸安普霉素Nebramycin II|||Ai3-29795；Nebramycin II|||Ai3-29795|||硫酸安普霉素|||硫酸阿布拉霉素
Apramycin sulfate (Nebramycin II) is an aminoglycoside antibiotic.
价 格：￥电议型 号：T1084产 地：中国大陆
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T10835L1Cletoquine hydrochloride；盐酸氯托喹Cletoquine hydrochloride( 4298-15-1 Free base)；Cletoquine hydrochlorid
Cletoquine hydrochloride is a major active metabolite of Hydroxychloroquine. Cletoquine hydrochloride is a Chloroquine derivative and exhibits the ability to against the chikungunya virus (CHIKV). Cletoquine hydrochloride exhibits antimalarial effects.
价 格：￥电议型 号：T10835L1产 地：中国大陆
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T10834CL656；化合物 T10834c-[2’FdAMP(S)-2’FdIMP(S)]；c-[2’FdAMP(S)-2’FdIMP(S)]
CL656 is a stimulator of interferon genes (STING) activator.
价 格：￥电议型 号：T10834产 地：中国大陆
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T10831L2Cl-amidine TFA；化合物 T10831L2Cl-amidine TFA
Cl-amidine TFA is an orally active inhibitor of peptidyl arginine deminase (PAD) (IC50s: 0.8 μM, 6.2 μM, and 5.9 μM for PAD1, PAD3, and PAD4). Cl-amidine induces apoptosis in cancer cells.
价 格：￥电议型 号：T10831L2产 地：中国大陆
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T10829CKI-7 free base；化合物 T10829CKI-7；CKI-7
CKI-7 free base is a potent and ATP-competitive inhibitor of casein kinase 1 (CK1; IC50: 6 μM; Ki: 8.5 μM) and a selective Cdc7 kinase inhibitor. CKI-7 free base also inhibits SGK, ribosomal S6 kinase-1 (S6K1), and MSK1.
价 格：￥电议型 号：T10829产 地：中国大陆
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T10820L1Ciraparantag acetate；化合物Ciraparantag acetateCiraparantag acetate(1438492-26-2 Free base)；Ciraparanta
Ciraparantag acetate, an anticoagulant reversal agent, is a small molecule specifically designed to bind noncovalently by charge-charge interaction to unfractionated heparin and low-molecular-weight heparin.?It shows binding characteristics that are similar to those of direct oral anticoagulants (DOACs).
价 格：￥电议型 号：T10820L1产 地：中国大陆
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T10820LCiraparantag TFA；化合物 T10820LPER977 TFA；PER977 TFA
Ciraparantag TFA is an inhibitor of thrombin and factor Xa. Ciraparantag is a broad-spectrum reversal agent for anticoagulants, including unfractionated heparin, low-molecular-weight heparin, and certain direct oral anticoagulants.
价 格：￥电议型 号：T10820L产 地：中国大陆
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T10818Ciprofibrate D6；化合物 T10818Ciprofibrate D6
Ciprofibrate D6 is a deuterium-labeled Ciprofibrate. Ciprofibrate is an agonist of peroxisome proliferator-activated receptor.
价 格：￥电议型 号：T10818产 地：中国大陆
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T1081Naftidrofuryl oxalate；萘呋胺酯 草酸盐Nafronyl oxalate|||Nafronyl oxalate salt；萘呋胺酯 草酸盐|||Nafronyl oxalate||
Naftidrofuryl oxalate (Nafronyl oxalate) is a drug used in the management of peripheral and cerebral vascular disorders. It is claimed to enhance cellular oxidative capacity and to be a spasmolytic. It may also be an antagonist at 5HT-2 serotonin receptors.
价 格：￥电议型 号：T1081产 地：中国大陆
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T10809LCHPG hydrochloride；化合物CHPG盐酸盐CHPG hydrochloride(170846-74-9 Free base)；CHPG hydrochloride(170846-74-
CHPG hydrochloride is a selective agonist of mGluR5.
价 格：￥电议型 号：T10809L产 地：中国大陆
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T10804CHMFL-PI3KD-317；化合物CHMFL-PI3KD-317CHMFL-PI3KD-317
CHMFL-PI3KD-317 is a highly potent, selective and orally active PI3Kδ inhibitor, with an IC50 of 6 nM, and exhibits over 10-1500 fold selectivity over other class I, II and III PIKK family isoforms, such as PI3Kα (IC50, 62.6 nM), PI3Kβ (IC50, 284 nM), PI3Kγ (IC50, 202.7 nM), PIK3C2A (IC50, >10000 nM), PIK3C2B (IC50, 882.3 nM), VPS34 (IC50, 1801.7 nM), PI4KIIIA (IC50, 574.1 nM) and PI4KIIIB (IC50, 300.2 nM). CHMFL-PI3KD-317 inhibits PI3Kδ-mediated Akt T308 phosphorylation in Raji cells, with an E
价 格：￥电议型 号：T10804产 地：中国大陆
