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1420-04-8

1420-04-8 structure
1420-04-8 structure
  • Name: Niclosamide olamine
  • Chemical Name: niclosamide-olamine
  • CAS Number: 1420-04-8
  • Molecular Formula: C15H15Cl2N3O5
  • Molecular Weight: 386.230
  • Catalog: Signaling Pathways Autophagy Autophagy
  • Create Date: 2018-07-29 17:16:14
  • Modify Date: 2024-01-04 20:35:59
  • Niclosamide olamine is an anthelmintic that disrupts mitochondrial metabolism in parasitic worms and animal models. Niclosamide olamine inhibits STAT3 (IC50 = 0.25 μM) and stimulates autophagy by reversibly inhibiting mammalian target of Rapamycin complex 1 (mTORC1) signaling.

Name niclosamide-olamine
Synonyms Luomiecide
Hl 2448
MFCD01941566
EINECS 215-811-7
Mollutox
2',5-dichloro-4'-nitrosalicylanilide
5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide - 1-propanamine (1:1)
Benzamide, 5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxy-, compd. with 1-propanamine (1:1)
clonitralid
Niclosamide ethanolamine salt
2’,5-dichloro-4’-nitrosalicylanilide - 2-aminoethanol (1:1)
BAYER73
(2-hydroxyethyl)ammonium 4-chloro-2-[(2-chloro-4-nitroanilino)carbonyl]phenolate
BAY-73
5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide—2-aminoethan-1-ol
Snanilcide
BAYER-6076
Clonitralide
NICLOSAMIDEL
5,2'-dichloro-4'-nitro-salicylanilide ethanolamine salt
5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide compound with 2-aminoethanol (1:1)
Description Niclosamide olamine is an anthelmintic that disrupts mitochondrial metabolism in parasitic worms and animal models. Niclosamide olamine inhibits STAT3 (IC50 = 0.25 μM) and stimulates autophagy by reversibly inhibiting mammalian target of Rapamycin complex 1 (mTORC1) signaling.
Related Catalog
Boiling Point 155-156 °C
Melting Point 91-93 °C(lit.)
Molecular Formula C15H15Cl2N3O5
Molecular Weight 386.230
Flash Point 149 °F
Exact Mass 385.059601
PSA 141.40000
LogP 4.09340
Stability Stable. Hydrolyzes in concentrated acidic or basic solutions.
Water Solubility soluble

CHEMICAL IDENTIFICATION

RTECS NUMBER :
VN8575000
CAS REGISTRY NUMBER :
1420-04-8
LAST UPDATED :
199607
DATA ITEMS CITED :
5
MOLECULAR FORMULA :
C13-H8-Cl2-N2-O4.C2-H7-N-O
MOLECULAR WEIGHT :
388.23
WISWESSER LINE NOTATION :
WNR CG DMVR BQ EG &Z2Q

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
85ARAE "Agricultural Chemicals," Thomson, W.T., 4 vols., Fresno, CA, Thomson Publications, 1976/77 revision Volume(issue)/page/year: 3,103,1976/1977
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
250 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
GUCHAZ Guide to the Chemicals Used in Crop Protection. (Information Canada, 171 Slater St., Ottawa, Ont., Canada) Volume(issue)/page/year: 6,126,1973 ** REPRODUCTIVE DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
336600 ug/kg
SEX/DURATION :
female 5-15 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus)
REFERENCE :
PCBPBS Pesticide Biochemistry and Physiology. (Academic Press, Inc., 1 E. First St., Duluth, MN 55802) V.1- 1971- Volume(issue)/page/year: 53,1,1995 *** U.S. STANDARDS AND REGULATIONS *** EPA FIFRA 1988 PESTICIDE SUBJECT TO REGISTRATION OR RE-REGISTRATION FEREAC Federal Register. (U.S. Government Printing Office, Supt. of Documents, Washington, DC 20402) V.1- 1936- Volume(issue)/page/year: 54,7740,1989
Safety Phrases S16-S26-S36/37/39-S45
RIDADR UN 1325 4.1/PG 2
WGK Germany 3
Packaging Group III
Hazard Class 4.1