Browsing Toxins By Category
T3DB ID | Name CAS Number | Formula Weight | Structure | Type | Mechanism of Toxicity |
---|---|---|---|---|---|
T3D2657 | alpha-Conotoxin (Conus geographus) Not Available | Not Available 1627.830 g/mol |
| alpha-Conotoxins act on postsynaptic membranes, where they inhibit nicotinic acetylcholine receptors in nerves and muscles. (L1107) Number of Targets: 15 | |
T3D2656 | omega-Conotoxin (Conus striatus) Not Available | Not Available 7628.040 g/mol |
| omega-Conotoxins act at presynaptic membranes, where they bind inhibit N-type voltage-dependent calcium channels. (L1107) Number of Targets: 1 | |
T3D2649 | Box jellyfish toxin (Chironex fleckeri) Not Available | Not Available 51389.865 g/mol |
| Box jellyfish toxin has potent hemolytic activity and may act as a pore-forming toxin, disrupting normal transmembrane ion concentration gradients in susceptible cells...more Number of Targets: 0 | |
T3D2648 | Neoverrucotoxin Not Available | Not Available 79669.850 g/mol |
| Neoverrucotoxin has hemolytic activities. (T170) Number of Targets: 0 | |
T3D2647 | Stonustoxin Not Available | Not Available 79523.640 g/mol |
| Stonustoxin induces hemolytic activities due to its ability to form pores in the cell membrane. It is also myotoxic and interferes irreversibly with neuromuscular func...more Number of Targets: 0 | |
T3D2646 | Hydralysin (Chlorohydra viridissima) Not Available | Not Available 26212.075 g/mol |
| Hydralysin is a cytolytic toxin. It binds to erythrocyte membranes and has weak hemolytic activity, probably mediated by oligomerization and pore formation. (T170) Number of Targets: 0 | |
T3D2645 | Brevetoxin 98112-41-5 | C49H68O14 881.056 g/mol |
| Brevetoxins are neurotoxins that bind to voltage-gated sodium channels in nerve cells, leading to disruption of normal neurological processes. (L1112) Number of Targets: 14 | |
T3D2643 | Vipoxin Not Available | Not Available 13827.665 g/mol |
| Vipoxin inhibits the binding of ligands to biogenic amine receptors including dopamine,
serotonin and alpha1/alpha2 adrenergic receptors. Vipoxin also exhibits hemoly...more Number of Targets: 28 | |
T3D2642 | Viperotoxin Not Available | Not Available 15554.775 g/mol |
| Viperotoxin is a presynaptic neurotoxin. (T170) Number of Targets: 0 | |
T3D2640 | Pseudechetoxin Not Available | Not Available 26474.445 g/mol |
| Pseudechetoxin blocks olfactory and retinal cyclic nucleotide-gated (CNG) ion channel currents. It forms high-affinity contacts with the pore turret region and most li...more Number of Targets: 2 | |
T3D2639 | Ohanin Not Available | Not Available 21173.945 g/mol |
| Ohanin is extremely neurotoxic, cardiotoxic, and cytotoxic. (L1102) Number of Targets: 0 | |
T3D2638 | Notexin 37233-96-4 | Not Available 13593.310 g/mol |
| Notexin is myotoxic and inhibits neuromuscular transmission by blocking acetylcholine release from the nerve termini. (T170) Number of Targets: 0 | |
T3D2637 | Nigroxin 9001-84-7 | Not Available 13341.125 g/mol |
| Nigroxin is myotoxic. (T170) Number of Targets: 0 | |
T3D2636 | Disintegrin echistatin (Echis carinatus) Not Available | Not Available 5424.090 g/mol |
| Disintegrins work by countering blood clotting steps, inhibiting the clumping of platelets. They inhibit fibrinogen interaction with platelet receptors expressed on gl...more Number of Targets: 2 | |
T3D2635 | Erabutoxin 59536-69-5 | Not Available 9136.510 g/mol |
| Erabutoxin binds with high affinity to muscular nicotinic acetylcholine receptors (nAChRs), and with low affinity to neuronal alpha-7 nAChRs. This produces peripheral ...more Number of Targets: 6 | |
T3D2633 | Acanthophin 126601-49-8 | Not Available 8386.795 g/mol |
| Acanthophin produces peripheral paralysis by blocking neuromuscular transmission at the postsynaptic site. It does this by binding to certain muscular and neuronal nic...more Number of Targets: 8 | |
T3D2631 | Heteroscodratoxin Not Available | Not Available 4003.400 g/mol |
| Heteroscodratoxin inhibits voltage-gated potassium channels by binding to the extracellular linker of the channel and shifting activation of the channel to more depola...more Number of Targets: 5 | |
T3D2630 | Sphingomyelinase D (Loxosceles intermedia) 9031-54-3 | Not Available 34158.125 g/mol |
| Sphingomyelinase D catalyzes the hydrolysis of sphingomyelin, inducing complement-dependent haemolysis, dermonecrosis, blood vessel permeability and platelet aggregati...more Number of Targets: 0 | |
T3D2629 | Hanatoxin 170780-01-5 | Not Available 4120.690 g/mol |
| Hanatoxin inhibits voltage-gated potassium channels by altering the gating energetics, which it does by occupying multiple binding sites on the channel. It can also in...more Number of Targets: 3 | |
T3D2628 | kappa-Atracotoxin (Hadronyche versuta) Not Available | Not Available 3685.155 g/mol |
| kappa-Atracotoxins inhibit insect voltage-gated potassium channels. (T170, L1812) Number of Targets: 0 | |
T3D2627 | mu-Agatoxin 120500-28-9 | Not Available 4272.715 g/mol |
| mu-Agatoxins modify presynaptic voltage-activated sodium channels in the neuromuscular joints of insects. Modifying sodium channels leads to an increased sensitivity o...more Number of Targets: 0 | |
T3D2626 | alpha-Agatoxin 128549-96-2 | C26H47N7O2 489.697 g/mol |
| alpha-Agatoxins block the glutamate-activated receptor channels in the neuronal postsynaptic terminals of insects and mammals, preventing excitory junction potential f...more Number of Targets: 11 | |
T3D2625 | Lopap Not Available | Not Available 22432.280 g/mol |
| Lopap activates thrombin by cleavage of prothrombin, causing thrombus formation, fibrinogen depletion, uncoagulable blood, decreased platelet count, inhibition of coll...more Number of Targets: 0 | |
T3D2624 | Melittin (Apis mellifera) 20449-79-0 | Not Available 7584.775 g/mol |
| Melittin has strong haemolytic activity. It integrates into cell membranes and has multiple effects, probably, as a result of its interaction with negatively charged p...more Number of Targets: 12 | |
T3D2590 | Calitoxin 118354-83-9 | Not Available 8727.960 g/mol |
| Calitoxin binds specifically to the voltage-gated sodium channel, thereby delaying its inactivation during signal transduction, resulting in strong stimulation of mamm...more Number of Targets: 14 |