CUCURBITACIN I

CUCURBITACIN I Basic information
Product Name:CUCURBITACIN I
Synonyms:ELATERICIN B;ELATERIN B;CUCURBITACIN I WITH HPLC;Cucurbitacin I hydrate;Elatericin B, JSI-124, NSC 521777, 2,16α,20,25-Tetrahydroxy-9-methyl-19-Nor-9β,10α-lanosta-1,5,23-triene-3,11,22-trione;(9β,10α,23E)-2,16α,20,25-Tetrahydroxy-9-methyl-19-norlanosta-1,5,23-triene-3,11,22-trione;Ibamarin;2,16a,20,25-Tetrahydroxy-9b-methyl-10a-19-norlanosta-1,5,23(E)-triene-3,11,22-trione
CAS:2222-07-3
MF:C30H42O7
MW:514.65
EINECS:218-736-8
Product Categories:Inhibitor;Herb extract;API;Tri-Terpenoids
Mol File:2222-07-3.mol
CUCURBITACIN I Structure
CUCURBITACIN I Chemical Properties
Melting point 148-150°C
Boiling point 698.3±55.0 °C(Predicted)
density 1.26±0.1 g/cm3(Predicted)
storage temp. -20°C
solubility ≥22.45 mg/mL in DMSO; insoluble in EtOH; ≥51.2 mg/mL in H2O with ultrasonic
pka8.51±0.70(Predicted)
form solid
color white to off-white
LogP2.330 (est)
Safety Information
Hazard Codes Xi,T+
Risk Statements 25-28
Safety Statements 1-22-45-36/37-28
RIDADR UN 2811 6.1/PG 1
WGK Germany 3
RTECS RC6200000
ToxicityLD50 oral in mouse: 5mg/kg
MSDS Information
CUCURBITACIN I Usage And Synthesis
UsesCucurbitacin I can be useful in the study of edible vitalmelon fruit extract and adipogenesis.
DefinitionChEBI: A cucurbitacin that is 9,10,14-trimethyl-4,9-cyclo-9,10-secocholesta-2,5,23-triene substituted by hydroxy groups at positions 2, 16, 20 and 25 and oxo groups at positions 1, 11 and 22.
Biological ActivitySelective inhibitor of STAT3/JAK2 signaling. Inhibits the activation of STAT3 and JAK2 and displays no activity on Src, Akt, ERK and JNK. Suppresses phosphotyrosine levels of STAT3, inhibits STAT3 DNA binding and STAT3-mediated gene expression. Induces apoptosis in cell lines expressing constitutively active tyrosine-phosphorylated STAT3.
Biochem/physiol ActionsCucurbitacin I (JSI-124) is a novel selective inhibitor of the janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3) signaling pathway with anti-proliferative and anti-tumor properties.
storageStore at -20°C
referencesblaskovich ma, sun j, cantor a et al. discovery of jsi-124 (cucurbitacin i), a selective janus kinase/signal transducer and activator of transcription 3 signaling pathway inhibitor with potent antitumor activity against human and murine cancer cells in mice.cancer res. 2003 mar 15;63(6):1270-9.yu h, lee h, herrmann a et al. revisiting stat3 signalling in cancer: new and unexpected biological functions.nat rev cancer. 2014 nov;14(11):736-46. doi: 10.1038/nrc3818.song j, liu h, li z et al. cucurbitacin i inhibits cell migration and invasion and enhances chemosensitivity in colon cancer. oncol rep. 2015 apr;33(4):1867-71. qi j, xia g, huang cr et al. jsi-124 (cucurbitacin i) inhibits tumor angiogenesis of human breast cancer through reduction of stat3 phosphorylation. am j chin med. 2015;43(2):337-47.kim hj, kim jk et al. antiangiogenic effects of cucurbitacin-i. arch pharm res. 2015 feb;38(2):290-8. yuan g, yan sf, xue h et al. cucurbitacin i induces protective autophagy in glioblastoma in vitro and in vivo. j biol chem. 2014 apr 11;289(15):10607-19.
CUCURBITACIN I Preparation Products And Raw materials
2-HEPTANONE,5-(HYDROXYMETHYL) 2-Allylcyclohexanone FITONE 2,2-DIMETHYL-3-OCTANONE 2-TERT-BUTYLPROPANE-1,3-DIOL 2-(TRANS-4'-N-BUTYL-CYCLOHEXYL)PROPANE-1,3-DIOL ADOXAL 2,2-DIMETHYL-3-HEPTANONE 2-Hydroxyhexanedial 2,7-dimethyloct-5-en-4-one dodec-3-en-1-al cucurbitacin R 2,25-diglucoside Cucurbitacin glucoside CUCURBITACIN I 2-(TRANS-4-ETHYLCYCLOHEXYL)PROPANE-1,3-DIOL 2,10-dimethylundecan-6-one 2-(TRANS-4-PENTYLCYCLOHEXYL)PROPANE-1,3-DIOL 1-CYCLOHEXENYL ACETONE

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