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Item number: TGM-T80443-50mg
Description: omega-Conotoxin MVIID (SNX-238) is a peptide from the Conus genus that inhibits the omega-Conotoxin-GVIA-sensitive, high-threshold calcium (Ca 2+) current in fish retinal ganglion cells [1]. Target: Calcium Channel
| Keywords: | SNX-238 |
| MW: | 2695.08 D |
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Item number: TGM-T80444-50mg
Description: Phlo1b (µ-TrTx-Phlo1b), a 35-amino acid peptide toxin, selectively inhibits Nav1.7 channels with minimal inhibition of Nav1.2 and Nav1.5 [1]. Target: Sodium Channel
| Keywords: | µ-TrTx-Phlo1b |
| MW: | 4140.71 D |
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Item number: TGM-T80445-50mg
Description: Phlo1a (µ-TrTx-Phlo1a), a 35-amino acid peptide toxin, demonstrates a weak inhibitory effect on Nav1.2 and Nav1.5 channels [1]. Meanwhile, Phlo1b acts as a selective inhibitor of the Nav1.7 channel. Target: Sodium Channel
| Keywords: | µ-TrTx-Phlo1a |
| MW: | 4106.69 D |
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Item number: TGM-T80446-50mg
Description: omega-Conotoxin FVIA is an inhibitor of N-type Ca2+ channels (Cav2.2), shown to alleviate mechanical and thermal pain abnormalities in a rat model of caudal nerve injury. This compound has potential utility in the research of potent analgesics with minimal side effects [1]. Target: Calcium Channel
| MW: | 2566.96 D |
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Item number: TGM-T80447-50mg
Description: Pardaxin P5, an antimicrobial peptide, inhibits Escherichia coli at a minimum inhibitory concentration (MIC) of 13 µM [1].
| CAS | 67995-63-5 |
| MW: | 3381.87 D |
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Item number: TGM-T80448-50mg
Description: omega-Conotoxin CVIF is a selective inhibitor of Ca v 2.2 channels, with an IC50 value of 34.3 nM in isolated rat DRG neurons, and exhibits weakly reversible blockade of Cav2.2 channels [1]. Target: Calcium Channel
| MW: | 2665.07 D |
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Item number: TGM-T80449-50mg
Description: omega-Conotoxin CVIE selectively inhibits voltage-gated Ca^2+ channels (Ca_v 2.2) [1]. Target: Calcium Channel
| MW: | 2638.99 D |
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Item number: TGM-T80450-50mg
Description: Pe1b (µ-TrTx-Pe1b) is a selective NaV1.7 channel inhibitor with an inhibitory concentration 50 (IC50) value of 167 nanomolar (nM) [1]. Target: Sodium Channel
| Keywords: | µ-TrTx-Pe1b |
| MW: | 3975.43 D |
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Item number: TGM-T80451-50mg
Description: Ceratotoxin-2 (CcoTx2) is a voltage-gated sodium channel inhibitor with half maximal inhibitory concentrations (IC50) of 8 nM for Na v 1.2/beta 1 and 88 nM for Na v 1.3/beta 1 [1]. Target: Sodium Channel
| Keywords: | beta-TRTX-cm1b, CcoTx2 |
| CAS | 880885-98-3 |
| MW: | 4092.67 D |
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Item number: TGM-T80452-50mg
Description: Ceratotoxin-1 (CcoTx1) is a peptide toxin that functions as an inhibitor of various voltage-gated sodium channel subtypes. It selectively inhibits Nav1.1/beta1, Nav1.2/beta1, Nav1.4/beta1, and Nav1.5/beta1 with IC50 values of 523 nM, 3 nM, 888 nM, and 323 nM, respectively. Additionally, Ceratotoxin-1 is...
| Keywords: | beta-TRTX-cm1a, CcoTx1 |
| MW: | 4044.58 D |
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Item number: TGM-T80453-50mg
Description: GLP-1 (1-36) amide (human, rat) is a molecular variant of the GLP-1 (7-36) amide and has the capacity to stimulate [14C]aminopyrine accumulation in enzymatically dispersed, enriched rat parietal cells [1].
| Keywords: | Glucagon-like Peptide 1 (1-36) amide (human, rat) |
| MW: | 4111.44 D |
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Item number: TGM-T80454-50mg
Description: BmK-M1, a scorpion-derived toxin, consists of a 64-amino acid polypeptide stabilized by four disulfide bridges. This compound functions as an inhibitor of the Na+ channel, classifying it as both a cardiotoxin and a neurotoxin [1]. Target: Sodium Channel
| MW: | 7217.13 D |
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