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Epigoitrin structure, CAS 1072-93-1

Epigoitrin

CAS Number1072-93-1

Synonyms5-vinyloxazolidin-2-thione; Goitrin; Epigoitrin; 5-vinyl-2-oxazolidinethione; Goitrine Epigoitrin; (5R)-5-Vinyl-1,3-oxazolidine-2-thione; (R)-5-Ethenyl-2-oxazolidinethione; goitrin, (±)-isomer; R-5-vinyl-2-thiooxazolidone; R-5-Vinyl-2-oxazolidinethione; 5-vinyloxazolidine-2-thione; DL-Goitrin; RS-Goitrin; 5-Vinyl-1,3-oxazolidine-2-thione; R-GOITRIN; UNII:O8KVD7J2P5; 5-Vinyloxazolidone-2-thione; 5-vinyl-2-thiooxazolidone; D-Goitrin

Molecular FormulaC5H7NOS

Molecular Weight129.18

Purity≥98 (HPLC)%

Density1.2±0.1 g/cm3

Boiling Point150.6±43.0 °C at 760 mmHg

Melting Point50ºC

Flash Point

Appearancepowder

EINECS

MSDSChineseEnglish

Symbol

Signal Word

Cat. No.: 2A-9026031 Purity: ≥98 (HPLC)%
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Quality Control of [ 1072-93-1 ] Purity: ≥98 (HPLC)% SDS Specification MoL

COA NMR CNMR HPLC LC-MS
Chemical & Physical Properties
CAS Number1072-93-1
Catalog No.2A-9026031
Chinese Name表告依春
Synonyms5-vinyloxazolidin-2-thione; Goitrin; Epigoitrin; 5-vinyl-2-oxazolidinethione; Goitrine Epigoitrin; (5R)-5-Vinyl-1,3-oxazolidine-2-thione; (R)-5-Ethenyl-2-oxazolidinethione; goitrin, (±)-isomer; R-5-vinyl-2-thiooxazolidone; R-5-Vinyl-2-oxazolidinethione; 5-vinyloxazolidine-2-thione; DL-Goitrin; RS-Goitrin; 5-Vinyl-1,3-oxazolidine-2-thione; R-GOITRIN; UNII:O8KVD7J2P5; 5-Vinyloxazolidone-2-thione; 5-vinyl-2-thiooxazolidone; D-Goitrin
Molecular FormulaC5H7NOS
Molecular Weight129.18
Purity≥98 (HPLC)
Density1.2±0.1 g/cm3
Boiling Point150.6±43.0 °C at 760 mmHg
Melting Point50ºC
Appearancepowder
Storage Condition2~8°C, dry
ApplicationEpigoitrin is a natural alkaloid found in isatis root and has antiviral activity. Epigoitrin reduces susceptibility to influenza viruses through mitochondrial antiviral signaling.
HTC2934999090
PubChem ID10047180
SMILESS=C1NC[C@H](O1)C=C
InChI1S/C5H7NOS/c1-2-4-3-6-5(8)7-4/h2,4H,1,3H2,(H,6,8)/t4-/m1/s1
InChI KeyUZQVYLOFLQICCT-SCSAIBSYSA-N
NACRES CodeNA.77
UNSPSC12352200
MSDSmsds/26031_1_1072_93_1.pdf
Use ofEpigoitrin is a natural alkaloid from Isatis indigotica, with antiviral activities. Epigoitrin reduces susceptibility to influenza virus via mitochondrial antiviral signaling[1][2]. Properties Name goitrine Synonym More Synonyms Epigoitrin Biological Activity Description Epigoitrin is a natural alkaloid from Isatis indigotica, with antiviral activities. Epigoitrin reduces susceptibility to influenza virus via mitochondrial antiviral signaling[1][2]. Related Catalog Research Areas >> Cancer Research Areas >> Infection References [1]. Luo Z, et al. Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro. Front Pharmacol. 2019 Feb 7;10:78. [2]. Xiao P, et al. Antiviral activities against influenza virus (FM1) of bioactive fractions and representative compounds extracted from Banlangen (Radix Isatidis). J Tradit Chin Med. 2016 Jun;36(3):369-76. Chemical & Physical Properties Molecular Formula C5H7NOS Exact Mass 129.024841 PSA 53.35000 Appearance of Characters solid Index of Refraction 1.570 InChIKey UZQVYLOFLQICCT-SCSAIBSYSA-N Toxicological Information CHEMICAL IDENTIFICATION RTECS NUMBER : CHEMICAL NAME : 2-Oxazolidinethione, 5-vinyl-, (R)- CAS REGISTRY NUMBER : LAST UPDATED : DATA ITEMS CITED : MOLECULAR FORMULA : C5-H7-N-O-S MOLECULAR WEIGHT : WISWESSER LINE NOTATION : T5MYOTJ BUS D1U1 HEALTH HAZARD DATA ACUTE TOXICITY DATA TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Unreported SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : JAFCAU Journal of Agricultural and Food Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB 57136, West End Stn., Washington, DC 20037) V.1- 1953- Volume(issue)/page/year: 17,483,1969 ** OTHER MULTIPLE DOSE TOXICITY DATA ** TYPE OF TEST : TDLo - Lowest published toxic dose ROUTE OF EXPOSURE : Subcutaneous SPECIES OBSERVED : Rodent - rat DOSE/DURATION : TOXIC EFFECTS : Liver - changes in liver weight Endocrine - changes in thyroid weight Blood - changes in serum composition (e.g. TP, bilirubin, cholesterol) REFERENCE : FCTOD7 Food and Chemical Toxicology. (Pergamon Press Inc., Maxwell House, Fairview Park, Elmsford, NY 10523) V.20- 1982- Volume(issue)/page/year: 20,279,1982 ** REPRODUCTIVE DATA ** TYPE OF TEST : TDLo - Lowest published toxic dose ROUTE OF EXPOSURE : Subcutaneous SEX/DURATION : female 8-9 day(s) after conception TOXIC EFFECTS : Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus) REFERENCE : FCTXAV Food and Cosmetics Toxicology. (London, UK) V.1-19, 1963-81. For publisher information, see FCTOD7. Volume(issue)/page/year: 18,159,1980 Safety Information Hazard Codes Xi HS Code 2934999090
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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