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CUCURBITACIN I

CAS No.
2222-07-3
Chemical Name:
CUCURBITACIN I
Synonyms
CUCURBITACIN I WITH HPLC;JSI-124;Ibamarin;ELATERIN B;NSC 521777;ELATERICIN B;CUCURBITACIN I;5-tetrahydroxy-;cucurbitacine(i);Cucurbitacin I-RM
CBNumber:
CB6480840
Molecular Formula:
C30H42O7
Molecular Weight:
514.65
MDL Number:
MFCD09971044
MOL File:
2222-07-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41

CUCURBITACIN I 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
pka 8.51±0.70(Predicted)
form solid
color white to off-white
InChIKey NISPVUDLMHQFRQ-KUIOOTTBNA-N
SMILES [C@@]12(C)CC(O)C(C(O)(C)C(=O)/C=C/C(O)(C)C)[C@@]1(C)CC(=O)[C@]1(C)C3C=C(C(=O)C(C)(C)C3=CC[C@@]21[H])O |&1:0,17,22,35,r|
LogP 2.330 (est)
FDA UNII SHQ47990PH
UNSPSC Code 41116107
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P301+P330+P331+P310
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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
Storage Class 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 1 Oral
Toxicity LD50 oral in mouse: 5mg/kg
NFPA 704
0
2 0

CUCURBITACIN I price More Price(50)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHL89464 Cucurbitacin I phyproof? Reference Substance 2222-07-3 10MG $655 2026-04-30 Buy
Sigma-Aldrich C4493 Cucurbitacin I hydrate ≥95% (HPLC), solid 2222-07-3 1mg $281 2026-04-30 Buy
Sigma-Aldrich 238590 Cucurbitacin I, Cucumis sativus L. A cell-permeable and irreversible bitter triterpenoid compound (NCI identifier: NSC 521777) that displays anti-proliferative and antitumor properties both in vitro and in vivo. 2222-07-3 1MG $270 2026-04-30 Buy
Cayman Chemical 14747 Cucurbitacin I ≥98% 2222-07-3 1mg $106 2026-04-30 Buy
Cayman Chemical 14747 Cucurbitacin I ≥98% 2222-07-3 5mg $262 2026-04-30 Buy
Product number Packaging Price Buy
PHL89464 10MG $655 Buy
C4493 1mg $281 Buy
238590 1MG $270 Buy
14747 1mg $106 Buy
14747 5mg $262 Buy

CUCURBITACIN I Chemical Properties,Uses,Production

Description

Cucurbitacin I is a naturally occurring tetracyclic triterpenoid compound with a variety of physiological effects, including induction of apoptosis and blockade of cell cycle progression in various cancer cells. It has also been shown to have anti-angiogenic activity. Cucurbitacin I inhibits the phosphorylation of vascular endothelial growth factor receptor-2 and fibroblast growth factor receptor-1, which are key regulators of endothelial cell function and angiogenesis. Therefore, Cucurbitacin I is considered a potential angiogenesis inhibitor candidate for cancer therapy[1].

Uses

Cucurbitacin I can be useful in the study of edible vitalmelon fruit extract and adipogenesis.

Definition

ChEBI: Cucurbitacin I is 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. It has a role as a plant metabolite and an antineoplastic agent. It is a cucurbitacin and a tertiary alpha-hydroxy ketone.

Biological Activity

Selective 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 Actions

Cucurbitacin 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.

storage

Store at -20°C

References

[1] HYEON JIN KIM Jin K K. Antiangiogenic effects of cucurbitacin-I[J]. Archives of Pharmacal Research, 2014. DOI:10.1007/s12272-014-0386-5.
blaskovich 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

Raw materials

Preparation Products

Global( 149)Suppliers
Supplier Tel Email Country ProdList Advantage
Jiaozuo Furuitang Pharmaceutical Co., Ltd. -- jzfrtcw@163.com China 8 58
Chengdu Bioanseis Phytochemicals Co., Ltd. 13518187787 632977132@qq.com China 315 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
Chengdu Biopurify Phytochemicals Ltd. +86-028-82633397 18982077548 cwb1@biopurify.cn China 2376 60
Shanghai Winherb Medical Technology Co., Ltd. 17301719108 13341702378 winherb@126.com China 1245 58
Haoyuan Chemexpress Co., Ltd. 021-58950125 info@chemexpress.com China 7545 61
MedChemexpress LLC 021-58955995 sales@medchemexpress.cn United States 4853 58
AdooQ BioScience, LLC +1 (866) 930-6790 info@adooq.com United States 2774 58

View Lastest Price from CUCURBITACIN I manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Cucurbitacin I pictures 2026-07-27 Cucurbitacin I
2222-07-3
$77.00-239.00 99.73% 10g TargetMol Chemicals Inc.
CUCURBITACIN I pictures 2019-07-06 CUCURBITACIN I
2222-07-3
$1.00 1G 98% 100KG Career Henan Chemical Co

CUCURBITACIN I Spectrum

1,2-dehydroelatericina 19-nor-9-beta,10-alpha-lanosta-1,5,23-triene-3,11,22-trione,9-methyl-2,16,20,2 JSI-124 2,16alpha,20,25-tetrahydroxy-9beta-methyl-10alpha-19-norlanosta-1,5,23(E)-triene-3,11,22-trione 5-tetrahydroxy- cucurbitacine(i) ELATERICIN B ELATERIN B CUCURBITACIN I 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 2,16α,20,25-tetrahydroxy-9β-methyl-10α-19-norlanosta-1,5,23(E)-triene-3,11,22-trione 19-Norlanosta-1,5,23-triene-3,11,22-trione, 2,16,20,25-tetrahydroxy-9-methyl-, (9b,10a,16a,23E)- CUCURBITACIN I(SH) CUCURBITACIN I hplc (9β,10α,16α,23E)-2,16,20,25-Tetrahydroxy-9-methyl-19-norlanosta-1,5,23-triene-3,11,22-trione 2,16α,20,25-tetrahydroxy-9-methyl-19-Nor-9β,10α-lanosta-1,5,23-triene-3,11,22-trione NSC 521777 Cucurbitacin I (JSI-124) calebassine/cucurbitacin Cucurbitacin I (Elatericin B 19-Norlanosta-1,5,23-triene-3,11,22-trione, 2,16,20,25-tetrahydroxy-9-methyl-, (9β,10α,16α,23E)- Cucurbitacin I-RM Cucurbitacin I(AS) Cucurbitacin I, 10 mM in DMSO Cucurbitacin I, Cucumis sativus L. Cucurbitacin I - Bio-X ? CUCURBITACIN I WITH HPLC 2222-07-3 2222-7-3 Inhibitor Herb extract API Tri-Terpenoids