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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T1456 | Doxorubicin | Hydroxydaunorubicin,Adriamycin | Topoisomerase , AMPK |
Doxorubicin (Adriamycin) is a Topoisomerase II (Top2) inhibitor with antineoplastic activity. | |||
T1020 | Doxorubicin hydrochloride | Adriamycin,Doxorubicin (Adriamycin) HCl,Hydroxydaunorubicin hydrochloride,NSC 123127 | Apoptosis , Mitophagy , HBV , HIV Protease , Topoisomerase , Antibacterial , Antibiotic , AMPK , Autophagy |
Doxorubicin hydrochloride (Adriamycin) belongs to the anthracycline class of antibiotics and is an inhibitor of human DNA topoisomerase I/II (IC50=0.8/2.67 μM). Doxorubicin hydrochloride exhibits cytotoxicity and antitum... | |||
T31567 | Doxorubicin-MVCP | MC-Val-Cit-PAB-Doxorubicin,MC-Val-Cit-PAB-Dox | |
Doxorubicin-MVCP (MC-Val-Cit-PAB-Doxorubicin) is a Doxorubicin derivative with an MC-Val-Cit-PAB linker. | |||
T18418 | N-(Iodoacetamido)-Doxorubicin | Others | |
N-(Iodoacetamido)-Doxorubicin is an ADC linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T70775 | Zoptarelin doxorubicin | ||
Zoptarelin doxorubicin, also known as AEZS-108, is an LHRH agonist. Zoptarelin doxorubicin is a peptide agonist of the gonadotropin releasing hormone-1 receptor (GnRH-1R) that is conjugated to the anthracycline antibio... | |||
T15161 | Doxorubicin-SMCC | Others | |
Doxorubicin-SMCC is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T29673 | Doxorubicinone | Adriamycinone,Adriamycin Aglycone,Doxorubicin Aglycone | |
Adriamycin Aglycone, also known as Doxorubicinone, is an oncolytic agent. It is a metabolite of Doxorubicin which binds to the DNA minor-groove. | |||
T77832 | Azide-PEG4-VC-PAB-Doxorubicin | ||
Azide-PEG4-VC-PAB-Doxorubicin is an agent-linker conjugate for antibody-drug conjugate (ADC) applications, consisting of the cytotoxic anthracycline antibiotic Doxorubicin attached via the Azide-PEG4-VC-PAB linker [1]. | |||
T27200 | DOX−NOP1 HCl | doxorubicin-NOP1 conjugate,doxorubicin-NOP1 HCl,DOX−NOP1 Hydrochloride | |
DOX−NOP1 is a molecular hybrid covalently joining doxorubicin (DOX) and NOP1. DOX−NOP1 showed similar increased toxicity toward resistant cancer cells and, in addition, lower cardiotoxicity than DOX. | |||
T11090 | MC-DOXHZN | Doxorubicin(6-maleimidocaproyl)hydrazone | Others |
Mc-doxhzn is a protein-binding prodrug of DOXUbicin (DNA topoisomerase II inhibitor) with acid sensitivity. | |||
TQ0049 | MC-DOXHZN hydrochloride | Doxorubicin(6-maleimidocaproyl)hydrazone hydrochloride | Topoisomerase |
MC-DOXHZN hydrochloride is an albumin-binding prodrug of Doxorubicin. Doxorubicin is a DNA topoisomerase II inhibitor. | |||
T4469 | Nemorubicin | Methoxymorpholinyldoxorubicin,PNU-152243A,PNU 152243 | Others |
Nemorubicin (PNU 152243) is a doxorubicin derivative that differs significantly from its parent drug in terms of spectrum of antitumor activity, metabolism and toxicity profile. The drug is active on tumors resistant to ... | |||
T6909 | NSC348884 | Apoptosis , p53 | |
NSC348884 is a nucleophosmin inhibitor disrupts oligomer formation and induces apoptosis, inhibits cell proliferation at an IC50 of 1.7-4.0 μM in distinct cancer cell lines. | |||
T6928 | Pantoprazole | SKF96022,BY1023 | Apoptosis , Proton pump , Autophagy |
Pantoprazole (BY1023) is a proton pump inhibitor used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease. | |||
T0161 | Pantoprazole Sodium Hydrate | SKF96022 sodium hydrate,BY1023 (sodium hydrate),SKF96022 (sodium hydrate) | Apoptosis , Potassium Channel , Proton pump , Autophagy |
Pantoprazole Sodium Hydrate (BY1023 (sodium hydrate)) is a proton pump inhibitor drug, used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease. | |||
T6929 | Pantoprazole sodium | Pantecta,SKF96022 sodium,SKF96022 (sodium),BY1023 (sodium),BY-1023 sodium,Pantoloc | Apoptosis , Others , Proton pump , HIF , Autophagy |
Pantoprazole sodium (Pantecta) is the sodium salt form of a substituted benzimidazole with proton pump inhibitor activity. Pantoprazole sodium is a lipophilic, weak base that crosses the parietal cell membrane and enters... | |||
T11090L1 | Aldoxorubicin hydrochloride | Aldoxorubicin hydrochloride (1361644-26-9 Free base) | Topoisomerase |
Aldoxorubicin hydrochloride is an albumin-binding prodrug of Doxorubicin, a DNA topoisomerase II inhibitor. Aldoxorubicin hydrochloride is released from albumin under acidic conditions. Aldoxorubicin hydrochloride exhibi... | |||
T40736 | Doxorubicinol hydrochloride | 13-Dihydroadriamycin hydrochloride | |
Doxorubicinol hydrochloride, also known as 13-Dihydroadriamycin hydrochloride, is a secondary alcohol metabolite derived from Doxorubicin. | |||
T25349 | Doxorubicinol | RP-27706,Antibiotic 27706RP,13-Dihydrodoxorubicin,Adriamycinol,RP 27706 | |
Doxorubicinol is the major circulating metabolite of doxorubicin with antineoplastic acitivity. | |||
T11090L | Aldoxorubicin | DOXO-EMCH,INNO-206 | Topoisomerase |
Aldoxorubicin has effective antitumor activities in various cancer cell lines and in murine tumor models. Aldoxorubicin is an albumin-binding prodrug of Doxorubicin (DNA topoisomerase II inhibitors). |