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T5853RubitecanRubitecan,RFS 2000,9-Nitrocamptothecin
Rubitecan is a DNA topoisomerase I inhibitor. It inhibits DNA topoisomerase I and increases the fraction of supercoiled DNA in a cell-free assay in a concentration-dependent manner.Rubitecan is a semisynthetic agent related to camptothecin with potent ant
价 格：￥电议型 号：T5853产 地：美洲
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T5S19529-Methoxycamptothecin9-Methoxycamptothecin,9-Methoxycamptothecin,
9-Methoxycamptothecin (MCPT) has antitumour activities through topoisomerase inhibition.
价 格：￥电议型 号：T5S1952产 地：美洲
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T8733Antrodin A；(2-氯苯基)二苯基甲醇camphorataanhydride A；(2-氯苯基)二苯基甲醇|||camphorataanhydride A
Antrodin A (camphorataanhydride A) (AdA) is one of the main active ingredients in the solid-state fermented A. camphorata mycelium. It protects the liver from alcohol damage by improving the antioxidant and anti-inflammatory capacity of the liver and maintaining the stability of the intestinal flora.
价 格：￥电议型 号：T8733产 地：中国大陆
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T83520(S)-Campesterol；化合物 (S)-Campesterol5-Ergosten-3β-ol；5-Ergosten-3β-ol
´S-Campesterol (5-Ergosten-3β-ol) is a plant-derived sterol, commonly known as a phytosterol [1].´
价 格：￥电议型 号：T83520产 地：中国大陆
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T8346810NH2-11F-Camptothecin；化合物 10NH2-11F-Camptothecin10NH2-11F-Camptothecin
10NH2-11F-Camptothecin, an antibody-drug conjugate (ADC), exhibits antitumor activity and is utilized in cancer research [1].
价 格：￥电议型 号：T83468产 地：中国大陆
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T832447Ethanol-10NH2-11F-Camptothecin；化合物 7Ethanol-10NH2-11F-Camptothecin7Ethanol-10NH2-11F-Camptothecin
7Ethanol-10NH2-11F-Camptothecin, an antibody drug conjugate (ADC), demonstrates inhibitory effects on tumor growth and is utilized in cancer research [1].
价 格：￥电议型 号：T83244产 地：中国大陆
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T832368-Azido-cAMP；化合物 8-Azido-cAMP8-Azido-cAMP
8-Azido-cAMP, a fluorescent analog of cAMP, serves as a prototype for cAMP detection [1]. This click chemistry reagent features an azide group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-bearing molecules. It is also competent for strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
价 格：￥电议型 号：T83236产 地：中国大陆
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T82786Campneoside II；化合物 Campneoside IICampneoside II
Campneoside II, a compound extracted from the wood of Paulownia tomentosa var. tomentosa, demonstrates remarkable anti-complement activity [1].
价 格：￥电议型 号：T82786产 地：中国大陆
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T82002Juniper camphor；化合物 Juniper camphorJuniper camphor
Juniper camphor, a sesquiterpene compound, is isolated from the high-boiling fraction of camphor blue oil [1].
价 格：￥电议型 号：T82002产 地：中国大陆
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T81834MC-GGFG-(7ethanol-10NH2-11F-Camptothecin)；化合物 MC-GGFG-(7ethanol-10NH2-11F-Camptothecin)MC-GGFG-(7eth
MC-GGFG-(7ethanol-10NH2-11F-Camptothecin) (compound 141) is a protease-cleavable drug-linker conjugate utilized in antibody-drug conjugates (ADCs), featuring an MC-GGFG linker that allows for enzymatic cleavage [1].
价 格：￥电议型 号：T81834产 地：中国大陆
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T81833MC-GGFG-AM-(10NH2-11F-Camptothecin)；化合物 MC-GGFG-AM-(10NH2-11F-Camptothecin)MC-GGFG-AM-(10NH2-11F-Cam
MC-GGFG-AM-(10NH2-11F-Camptothecin) is an antibody-drug conjugate (ADC) that exhibits antitumor activity by targeting TROp-2 with the sacituzumab antibody through a hydrolysable, pH-sensitive linker. It is utilized in cancer research [1].
价 格：￥电议型 号：T81833产 地：中国大陆
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T80282cPcAMP1/26；化合物 cPcAMP1/26cPcAMP1/26
cPcAMP1/26, an antimicrobial peptide, exhibits potent bactericidal activity against A. hydrophila and S. aureus by inducing depolarization of the bacterial plasma membrane and elevating intracellular ROS (Reactive Oxygen Species) levels [1].
价 格：￥电议型 号：T80282产 地：中国大陆
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T80147EcAMP3；化合物 EcAMP3EcAMP3
EcAMP3, a hairpin-like peptide, exhibits both antifungal and antibacterial properties. It belongs to the EcAMP precursor family characterized by seven identical cysteine motifs: C1XXXC2(11–13)C3XXXC4 [1].
价 格：￥电议型 号：T80147产 地：中国大陆
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T798839-Chloromethyl-10-hydroxy-11-F-Camptothecin；化合物 9-Chloromethyl-10-hydroxy-11-F-Camptothecin9-Chlorom
9-Chloromethyl-10-hydroxy-11-F-Camptothecin, a novel derivative of camptothecin, functions as a DNA topoisomerase I (Topo I) inhibitor with potential applications in anticancer research [1].
价 格：￥电议型 号：T79883产 地：中国大陆
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T7959(+)-ISOPINOCAMPHEOL；(1S,2S,3S,5R)-(+)-异松蒎醇(+)-ISOPINOCAMPHEOL
(+)-ISOPINOCAMPHEOL is a natural product.
价 格：￥电议型 号：T7959产 地：中国大陆
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T778207-Aminomethyl-10-methyl-11-fluoro camptothecin；化合物 7-Aminomethyl-10-methyl-11-fluoro camptothecin7-A
7-Aminomethyl-10-methyl-11-fluoro camptothecin, serving as a cytotoxic component of the antibody-drug conjugate (ADC) MC-AAA-NHCH2OCH2COO-7-aminomethyl-10-methyl-11-fluoro camptothecin, is employed in the synthesis of camptothecin ADCs [1].
价 格：￥电议型 号：T77820产 地：中国大陆
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T77701FL118；化合物FL118FL 118|||FL-118|||10,11-(Methylenedioxy)-20(S)-camptothecin；FL 118|||FL-118|||10,11-(M
FL118 is a novel survivin inhibitor that inhibits cancer stem cell-like properties.FL118 is a novel camptothecin analog with anticancer activity that inhibits epithelial-mesenchymal transition through the Wnt/β-catenin signaling pathway, thereby inhibiting migration and invasion of human breast cancer cells.
价 格：￥电议型 号：T77701产 地：中国大陆
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T75134MC-GGFG-AM-(10Me-11F-Camptothecin)；化合物 MC-GGFG-AM-(10Me-11F-Camptothecin)MC-GGFG-AM-(10Me-11F-Campto
MC-GGFG-AM-(10Me-11F-Camptothecin) acts as a linker-payload conjugate in the synthesis of ZW251, an antibody-drug conjugate (ADC) designed to target human GPC3. This ADC comprises a humanized IgG1 antibody attached to ZD06519, a novel camptothecin-based topoisomerase 1 inhibitor, through a maleimide-anchor and a cleavable glycyl glycyl phenylalanyl glycine (GGFG)-aminomethyl (AM) linker. ZW251 exhibits strong affinity for GPC3 in both human and cynomolgus monkey cells. It is characterized by rap
价 格：￥电议型 号：T75134产 地：中国大陆
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T74654-Methylbenzylidene camphor；4-甲基苄亚基樟脑Enzacamene|||4-MBC；Enzacamene|||4-甲基苄亚基樟脑|||3-(4-甲基苯亚甲基)樟脑|||4-
4-Methylbenzylidene camphor is an ultraviolet light blocker used in cosmetics and sunscreen preparations ,specifically UV B radiation, also has estrogenic activities.
价 格：￥电议型 号：T7465产 地：中国大陆
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T73708Sp-cAMPS triethylamine；化合物 Sp-cAMPS triethylamineSp-cAMPS triethylamine
Sp-cAMPS triethylamine, a cAMP analog, serves as a potent activator of cAMP-dependent PKA I and II and acts as a competitive inhibitor of phosphodiesterase (PDE3A) with a K i of 47.6 ?M. Additionally, it binds the PDE10 GAF domain with an EC 50 of 40 μM [1] [2] [3].
价 格：￥电议型 号：T73708产 地：中国大陆
