Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15180 |
Duocarmycin A
|
Caspase | Apoptosis; Proteases/Proteasome |
Duocarmycin A, an antitumor antibiotic, is a DNA alkylator and efficiently alkylates adenine N3 at the 3′ end of AT-rich sequences in the DNA. Duocarmycin A, as a chemotherapeutic agent, results in HLC-2 cells typically apoptotic changes. | |||
T11120 |
Duocarmycin TM
|
DNA Alkylation; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Duocarmycin TM 是一种有抗肿瘤活性的抗生素,也是一种 DNA 烷化剂。 | |||
T73948 | Duocarmycin DM | ||
Duocarmycin DM,一种DNA小沟烷基化剂(DNA minor-groove alkylator),作为抗体活性分子结合物(ADCs)的毒素,因其独特结构显示出抗癌活性。 | |||
T63523 |
Duocarmycin analog-2
|
||
Duocarmycin analog-2 是有效的 DNA 烷基化剂,表现出抗肿瘤作用,能够用于免疫偶联物的合成。 | |||
T11117 |
Duocarmycin MB
|
Others | Others |
Duocarmycin MB can be used against multi-drug resistant cell lines. Duocarmycin MB is an antibody drug conjugates (ADCs) toxin. Duocarmycin is a DNA alkylating agent that binds in the minor groove. | |||
T11116 |
Duocarmycin MA
|
Others | Others |
Duocarmycin MA can be used against multi-drug resistant cell lines.Duocarmycin MA is an antibody drug conjugates (ADCs) toxin. Duocarmycin is a DNA alkylating agent that binds in the minor groove. | |||
T11119 |
Duocarmycin DM free base
Duocarmycin |
Others | Others |
Duocarmycin is a DNA minor groove binding alkylating agent and explored as drug–antibody conjugates (ADCs) . Duocarmycin is based on its characteristic curved indole structure and a spirocyclopropylcyclohexadienone electrophile to act anticancer activity. | |||
T12813L |
Seco-Duocarmycin SA
|
DNA Alkylation | DNA Damage/DNA Repair |
Seco-Duocarmycin SA is a highly potent DNA alkylator used as an ADC cytotoxin. | |||
T12813 |
(S)-Seco-Duocarmycin SA
|
Others | Others |
(S)-Seco-Duocarmycin SA is a DNA alkylator, acts as a ADC cytotoxin for antibody-drug conjugates. | |||
T70462 |
Pibrozelesin
|
||
Pibrozelesin is a water-soluble derivative of duocarmycin B2 that alkylates DNA by binding to adenine-thymine (A-T)-rich sequences in the minor groove of DNA, thereby inhibiting DNA replication and inducing apoptosis. | |||
T17982 |
Fmoc-Val-Cit-PAB-Duocarmycin TM
|
Others | Others |
Fmoc-Val-Cit-PAB-Duocarmycin TM is a drug-linker conjugate designed for antibody-drug conjugation (ADC), utilizing the antitumor antibiotic Duocarmycin TM. It is connected through the linker Fmoc-Val-Cit-PAB. | |||
T18324 |
MC-Val-Cit-PAB-duocarmycin chloride
MC-Val-Cit-PAB-duocarmycin |
Others | Others |
MC-Val-Cit-PAB-duocarmycin is an antibody-drug conjugate (ADC) linker that combines duocarmycin, a potent DNA minor groove-binding alkylating agent, with an antitumor drug through the MC-Val-Cit-PAB linker, exhibiting significant antitumor activity. | |||
T38611 |
Seco-DUBA
|
||
Seco-DUBA, a duocarmycin (DUBA) prodrug, possess two hydroxyl groups suitable for antibody coupling through a linker. This compound, serving as a precursor, enables the synthesis of antibody-drug conjugates (ADCs). | |||
T11115 |
Duocarmycin GA
|
Others | Others |
Duocarmycin GA, an antibody drug conjugate (ADC) toxin and a DNA alkylating agent, effectively targets and binds in the minor groove of DNA. It is particularly potent against multi-drug resistant cell lines, offering a strategic approach in combating resistance. |