Introduction:Basic information about CAS 29876-14-0|Nicotredole, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Nicotredole |
|---|
| CAS Number | 29876-14-0 | Molecular Weight | 265.310 |
|---|
| Density | 1.2±0.1 g/cm3 | Boiling Point | 588.4±35.0 °C at 760 mmHg |
|---|
| Molecular Formula | C16H15N3O | Melting Point | / |
|---|
| MSDS | / | Flash Point | 309.7±25.9 °C |
|---|
Names
| Name | N-[2-(1H-indol-3-yl)ethyl]pyridine-3-carboxamide |
|---|
| Synonym | More Synonyms |
|---|
Nicotredole BiologicalActivity
| Description | Nicotredole (Tryptamide) is an orally active anti-inflammatory and analgesic agent. Nicotredole exhibits evident antiinflammatory effects of potency comparable with Phenylbutazone. Nicotredole has only weak ulcerogenic activity[1][2][3]. |
|---|
| Related Catalog | Signaling Pathways >>Others >>OthersResearch Areas >>Inflammation/Immunology |
|---|
| In Vitro | Nicotredole inhibits prostaglandin synthetase activity in vitro[1]. |
|---|
| In Vivo | Nicotredole produces antiinflammatory effects in carrageenin-induced rat paw oedema[1]. Nicotredole reverses pyrogen-induced hyperthermia in rats, elicits analgesic effects in rats, prolongs the time of hexobarbital sleep in rats and inhibits locomotor activity in rats and mice[1]. Nicotredole (i.p.) has LD50s of 1260 mg/kg and 1980 mg/kg for male rats and male mice, respectively[1]. Nicotredole (p.o.) has LD50s of 8.5 g/kg and 9.3 g/kg for male rats and male mice, respectively[1]. Nicotredole (25 mg/kg; p.o. or i.p.) undergoes fast absorption (t1/2=4.92-17.5 min) and elimination (t1/2=55.72-74.52 min), can reach Cmax (11-13 μg/cm3) after 30 min, and gives AUC values in the range of 21.40-27.30 (μg•h/cm3)[2]. |
|---|
| References | [1]. Herman ZS, et, al. Basic pharmacological properties of a novel antiinflammatory drug tryptamide. Pol J Pharmacol Pharm. Nov-Dec 1987;39(6):729-36. [2]. Szumiło H. Pharmacokinetics of tryptamide following oral and intraperitoneal administration in rats. Acta Pol Pharm. 1990;47(1-2):19-22. [3]. Kulig D, et, al. A comparison of anti-inflammatory, analgesic and ulcerogenic action of tryptamide, ibuprofen and piroxicam. Pol J Pharmacol Pharm. Nov-Dec 1987;39(6):769-72. |
|---|
Chemical & Physical Properties
| Density | 1.2±0.1 g/cm3 |
|---|
| Boiling Point | 588.4±35.0 °C at 760 mmHg |
|---|
| Molecular Formula | C16H15N3O |
|---|
| Molecular Weight | 265.310 |
|---|
| Flash Point | 309.7±25.9 °C |
|---|
| Exact Mass | 265.121521 |
|---|
| PSA | 57.78000 |
|---|
| LogP | 1.94 |
|---|
| Vapour Pressure | 0.0±1.6 mmHg at 25°C |
|---|
| Index of Refraction | 1.669 |
|---|
| InChIKey | ZDAZUJBASMCUAK-UHFFFAOYSA-N |
|---|
| SMILES | O=C(NCCc1c[nH]c2ccccc12)c1cccnc1 |
|---|
Toxicological Information
CHEMICAL IDENTIFICATION - RTECS NUMBER :
- QS4476800
- CHEMICAL NAME :
- Nicotinamide, N-(2-indol-3-ylethyl)-
- CAS REGISTRY NUMBER :
- 29876-14-0
- BEILSTEIN REFERENCE NO. :
- 0242441
- LAST UPDATED :
- 199612
- DATA ITEMS CITED :
- 3
- MOLECULAR FORMULA :
- C16-H15-N3-O
- MOLECULAR WEIGHT :
- 265.34
- WISWESSER LINE NOTATION :
- T56 BMJ D2MV- CT6NJ
HEALTH HAZARD DATAACUTE TOXICITY DATA - TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intraperitoneal
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 1250 mg/kg
- TOXIC EFFECTS :
- Behavioral - somnolence (general depressed activity)
- REFERENCE :
- DPHFAK Dissertationes Pharmaceuticae et Pharmacologicae. (Warsaw, Poland) V.18-24, 1966-72. For publisher information, see PJPPAA. Volume(issue)/page/year: 22,313,1970 ** REPRODUCTIVE DATA **
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- DOSE :
- 90 mg/kg
- SEX/DURATION :
- female 6-14 day(s) after conception
- TOXIC EFFECTS :
- Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus)
- REFERENCE :
- PJPPAA Polish Journal of Pharmacology and Pharmacy. (ARS Polona, POB 1001, 00-068 Warsaw 1, Poland) V.25- 1973- Volume(issue)/page/year: 39,779,1987
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- DOSE :
- 4500 mg/kg
- SEX/DURATION :
- female 6-14 day(s) after conception
- TOXIC EFFECTS :
- Reproductive - Effects on Embryo or Fetus - fetal death
- REFERENCE :
- PJPPAA Polish Journal of Pharmacology and Pharmacy. (ARS Polona, POB 1001, 00-068 Warsaw 1, Poland) V.25- 1973- Volume(issue)/page/year: 39,779,1987
|
Safety Information
Synonyms
| nicotredole |
| 3-Pyridinecarboxamide, N-[2-(1H-indol-3-yl)ethyl]- |
| Tryptamide |
| N-Nicotinoyltryptamide |
| N-[2-(1H-Indol-3-yl)ethyl]nicotinamide |