- BCTC
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- $31.00
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2026-07-27
- CAS:393514-24-4
- Purity: 99.74%
- Supply Ability: 10g
- BCTC
-
- $1.00
-
2019-12-23
- CAS:393514-24-4
- Min. Order: 1KG
- Purity: 98% HPLC
- Supply Ability: 10t
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| Product Name: | BCTC | | Synonyms: | BCTC;4-(3-Chloro-2-pyridinyl)-N-[4-(1,1-dimethylethyl)phenyl]-1-piperazinecarboxamide;4-(3-Chloro-2-pyridinyl)-N-[4-(1,1-diMethylethyl)phenyl]-1-piperazinecarboxaMide (BCTC);N-(4-tert-butylphenyl)-4-(3-chloropyridin-2-yl)piperazine-1-carboxamide;1-Piperazinecarboxamide, 4-(3-chloro-2-pyridinyl)-N-[4-(1,1-dimethylethyl)phenyl]-;BCTC, inhibitor of TRPV1;BCTC, 10 mM in DMSO | | CAS: | 393514-24-4 | | MF: | C20H25ClN4O | | MW: | 372.89 | | EINECS: | | | Product Categories: | Vanilloid/TRPV channel | | Mol File: | 393514-24-4.mol |  |
| Melting point | 150-152℃ | | Boiling point | 561.6±50.0 °C(Predicted) | | density | 1.229±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | solubility | DMSO: >10mg/mL | | pka | 13.95±0.70(Predicted) | | form | powder | | color | white to beige | | Sensitive | Light Sensitive | | Stability: | Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stord at -20°C for up to 2 months. | | InChI | InChI=1S/C20H25ClN4O/c1-20(2,3)15-6-8-16(9-7-15)23-19(26)25-13-11-24(12-14-25)18-17(21)5-4-10-22-18/h4-10H,11-14H2,1-3H3,(H,23,26) | | InChIKey | ROGUAPYLUCHQGK-UHFFFAOYSA-N | | SMILES | N1(C(NC2=CC=C(C(C)(C)C)C=C2)=O)CCN(C2=NC=CC=C2Cl)CC1 |
| Hazard Codes | Xn | | Risk Statements | 22 | | WGK Germany | 3 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral |
| Description | BCTC (393514-24-4) is a vanilloid receptor I (TRPV1) blocker, IC50 = 35 nM for capsaicin-induced and 6 nM for acid-induced TRPV1 activation. Displays analgesic activity in rat models of neuropathic pain. BCTC is orally active and cell permeable. | | Uses | BCTC is a antagonists of TRPA1 and TRPV1, a non-selective cation channel gated by noxious heat, vanilloids and extracellular protons. BCTC inhibits both capsaicin and proton activation. | | Definition | ChEBI: 1-piperazinecarboxamide, 4-(3-chloro-2-pyridinyl)-n-[4-(1,1-dimethylethyl)phenyl]- is a member of piperazines and a member of pyridines. | | in vivo | BCTC (1-30 mg/kg; Oral gavage; Single dose) can inhibit inflammatory and neuropathic heat pain and mechanical hyperalgesia in Sprague-Dawley rats by targeting VR1, which has analgesic effect[2].
BCTC (10-100 mg/kg; Oral gavage, Twice daily for 4 weeks) improves the insulin resistance and systemic glucose and lipid metabolism, and increase insulin secretion in diabetic ob/ob mice[5].
| Animal Model: | Capsaicin-induced Sprague-Dawley rats model[2] | | Dosage: | 1 mg/kg, 3 mg/kg, 10 mg/kg, 30 mg/kg | | Administration: | Oral gavage (p.o.), Single dose. Before capsaicin (HY-10448) treatment (30 μg; intraplantar injection; Single dose) | | Result: | Inhibited capsaicin-mediated thermal hyperalgesia in a dose-dependent manner. |
| Animal Model: | Freund’s complete adjuvant (FCA) Sprague-Dawley rats model[2] | | Dosage: | 1 mg/kg, 3 mg/kg, 10 mg/kg, 30 mg/kg | | Administration: | Oral gavage (p.o.), Single dose. After 100 % FAC treatment (50 μL; intraplantar injection; Single dose) | | Result: | Significantly reduced FAC-induced inflammation-related thermal pain and mechanical hyperalgesia, and extended the inhibitory effect of mechanical hyperalgesia to 6 h at high doses (10 mg/kg, 30 mg/kg). |
| Animal Model: | Partial sciatic nerve ligation Sprague-Dawley rats model[2] | | Dosage: | 1 mg/kg, 3 mg/kg, 10 mg/kg, 30 mg/kg | | Administration: | Oral gavage (p.o.), Single dose. After partial sciatic nerve ligation. | | Result: | Reduced post-operative abnormal tactile pain and mechanical hyperalgesia in a dose-dependent manner. |
| Animal Model: | Particularly strong insulin resistance and hyperinsulinemia ob/ob mice model[5] | | Dosage: | 10 mg/kg, 30 mg/kg, 100 mg/kg | | Administration: | Oral gavage (p.o.); Twice daily for 4 weeks | | Result: | Reduced plasma triglyceride and glucose area under the curve (AUC) level.
Decreased calcitonin gene-related peptide (CGRP) levels in a dose-dependent manner.
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| | storage | Room temperature | | References | [1] KENNETH J VALENZANO. N-(4-tertiarybutylphenyl)-4-(3-chloropyridin-2-yl)tetrahydropyrazine -1(2H)-carbox-amide (BCTC), a novel, orally effective vanilloid receptor 1 antagonist with analgesic properties: I. in vitro characterization and pharmacokinetic properties.[J]. Journal of Pharmacology and Experimental Therapeutics, 2003, 306 1: 377-386. DOI:10.1124/jpet.102.045674
[2] JAMES D POMONIS. N-(4-Tertiarybutylphenyl)-4-(3-cholorphyridin-2-yl)tetrahydropyrazine -1(2H)-carbox-amide (BCTC), a novel, orally effective vanilloid receptor 1 antagonist with analgesic properties: II. in vivo characterization in rat models of inflammatory and neuropathic pain.[J]. Journal of Pharmacology and Experimental Therapeutics, 2003, 306 1: 387-393. DOI:10.1124/jpet.102.046268 |
| | BCTC Preparation Products And Raw materials |
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