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3-cpa

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  • Inhibitors & Agonists
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Declopramide
OXI-104, IMO-B, 3-Chloroprocainamide
T27138891-60-1In house
Declopramide (OXI-104) is a novel chemosensitizer with antitumor activity that induces apoptosis and can be used to study colorectal cancer and inflammatory bowel disease.
  • $176 TargetMol
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TargetMol | Inhibitor Sale
Lupeol
Monogynol B, Farganasterol, Fagarasterol, Clerodol, (3β,13ξ)-Lup-20(29)-en-3-ol
T2895545-47-1
Lupeol (Monogynol B) is a novel androgen receptor inhibitor with anti-inflammatory and antioxidant activity.
  • $30
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TargetMol | Citations Cited
Oleoyl 3-carbacyclic Phosphatidic Acid
3-ccPA 18:1
T84482779333-58-3
Cyclic Phosphatidic Acids (cPAs) are naturally occurring lysophosphatidic acid (LPA) analogs, characterized by a 5-membered ring formed between the sn-2 hydroxy group and the sn-3 phosphate. Carba-derivatives of cPA (ccPA) modify the sn-2 (2-ccPA) or sn-3 (3-ccPA) linkage, hindering the conversion of cPA into LPA. Oleoyl 3-Carbacyclic Phosphatidic Acid (3-ccPA 18:1) incorporates the 18:1 fatty acid oleate at the sn-1 position on the glycerol backbone, acting as a cyclic LPA analog. This compound, at a concentration of 25 μM, blocks MM1 cells' transcellular migration through mesothelial cell monolayers induced by fetal bovine serum (by 90.1%) or LPA (by 99.9%), without impeding cell proliferation. Additionally, 3-ccPA 18:1, in the 0.1-1.0 μM range, notably suppresses autotaxin, which plays a vital role in various cancer cell behaviors including survival, growth, migration, invasion, and metastasis.
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8-10 weeks
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