Inquiry Basket
| Catalog | Product Name | CAS Number |
|---|---|---|
| BADC-00283 | LK-66 M | |
| A muscarinic receptors antagonist. | Inquiry | |
| BADC-00291 | M2-Nitrodienamine | |
| Nitrodienamine is an inhibitor of Ca2+/Mg2+ ATPase. | Inquiry | |
| BADC-00292 | M3-Nitrodienamine | |
| Nitrodienamine is an inhibitor of Ca2+/Mg2+ ATPase. | Inquiry | |
| BADC-00293 | M4-Nitrodienamine | |
| Nitrodienamine is an inhibitor of Ca2+/Mg2+ ATPase. | Inquiry | |
| BADC-00294 | M5-Nitrodienamine | |
| Nitrodienamine is an inhibitor of Ca2+/Mg2+ ATPase. | Inquiry | |
| BADC-00298 | Muscarinic toxin 2 | |
| Muscarinic toxin 2 (MT2) is one member of a family of small peptides of 65 amino acid residues of around 7076 daltons in molecular weight derived from the venom of African mamba snakes (Dendroaspis angusticeps), which target the different muscarinic receptor subtypes. Muscarinic toxins like the nicotinic toxins have the three-finger fold structure, characteristic of the large superfamily of toxins that act at cholinergic synapses. | Inquiry | |
| BADC-00305 | Penetran Cl | |
| Synthetic, an inhibitor of high-affinity choline uptake (HAChU) in synaptosomes. | Inquiry | |
| BADC-00312 | Q Bu-i | |
| Synthetic, nicotinic AChR. Rigid bicyclic analog of TMA and TEA. | Inquiry | |
| BADC-00313 | Q Pr | |
| Synthetic, nicotinic AChR. Rigid bicyclic analog of TMA and TEA. | Inquiry | |
| BADC-00315 | Quireston-A | |
| Synthetic, a potent inhibitor of high-affinity choline uptake (HAChU) in synaptosomes. | Inquiry | |
| BADC-00322 | [Tyr2] Scyllatoxin | |
| [Tyr2]-Scyllatoxin allows labelling by iodination. 31-amino acid polypeptide with 3 disulfide bridges. Synthetic, originally from Leiurus quinquestriatus hebraeus scorpion venom. A blocker of Apamin-sensitive Ca2+-activated K+ channels. | Inquiry | |
| BADC-00323 | Sevedindione | |
| Sevedindione presents an antiarrhythmic activity on arrhythmias caused by Aconitine. | Inquiry | |
| BADC-00081 | Ungerine Nitrate | |
| Alkaloid , from plants of the Ungernia genus, Amaryllidaceae. | Inquiry | |
| BADC-00723 | N-Acetyl-Calicheamicin | 108212-76-6 |
| N-Acetyl-Calicheamicin is a potent enediyne antitumor antibiotic that could be a potential cytotoxic DNA-binding agent in antibody-drug-conjugation (ADC). Calicheamicin is a naturally occurring hydrophobic enediyne antibiotic that was isolated from the actinomycete Micromonospora echinospora calichensis. | Inquiry | |
| BADC-00009 | DM1-SMCC | 1228105-51-8 |
| DM1 with a reactive linker SMCC, which can react with antibody to make antibody drug conjugate, as a potent EGFR inhibitor and it overcomes resistant to EGFR. | Inquiry | |
| BADC-00153 | Chlorotoxin | 163515-35-3 |
| Chlorotoxin (Cltx) is a neurotoxin that was originally isolated from the venom of Leiurus quinquestriatus. Chlorotoxin is a specific ligand of glioma cells. Chlorotoxin binds to Cl- channels (small conductance epithelial chloride channels) in the brain and spinal cord and inhibits Cl- influx. | Inquiry | |
| BADC-00363 | Aldoxorubicin hydrochloride | 480998-12-7 |
| Aldoxorubicin is a prodrug of doxorubicin that binds to serum albumin immediately after administration through an acid-sensitive hydrazone linker and is subsequently transported to tumor tissues where the acidic environment cleaves the linker and facilitates delivery of a tumor-targeted drug payload. | Inquiry | |
| BADC-00189 | Ansamitocin P 3' | 66547-09-9 |
| Ansamitocin P 3' is an isomer of Ansamitocin P-3, a potent anti-tumor maytansinoid antibiotic found in Actinosynnema pretiosum, a maytansine analog which displays potent cytotoxicity against the human solid tumor cell lines A-549 and HT-29. | Inquiry | |
| BADC-00008 | Val-Cit-PAB-MMAE | 644981-35-1 |
| Val-Cit-PAB-MMAE, a tubulin polymerase inhibitor, is a drug-linker conjugate for ADC. It contains an ADC linker (peptide Val-Cit-PAB) and a potent tubulin inhibitor MMAE. | Inquiry | |
| BADC-00010 | DM1-SPP | 452072-20-7 |
| DM1 with a reactive linker SPP, which can react with antibody to make antibody drug conjugate, as a potent EGFR inhibitor and it overcomes resistant to EGFR. | Inquiry |
