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GGTI 2133 (trifluoroacetate salt)

CAS No.
1217480-14-2
Chemical Name:
GGTI 2133 (trifluoroacetate salt)
Synonyms
GGTI 2133 TFA;GGTI 2133 (trifluoroacetate salt);N-[4-[(1H-imidazol-5-ylmethyl)amino]-2-(1-naphthalenyl)benzoyl]-L-leucine,2,2,2-trifluoroacetatesalt
CBNumber:
CB04814593
Molecular Formula:
C29H29F3N4O5
Molecular Weight:
570.57
MDL Number:
MOL File:
1217480-14-2.mol
MSDS File:
SDS
Last updated:2026-05-27 22:45:03

GGTI 2133 (trifluoroacetate salt) Properties

Melting point 103-118.5 °C
storage temp. -20°C
solubility DMSO: 25 mg/ml
form A crystalline solid
color white to beige
InChIKey FXXUNOYBYJFSRB-UQIIZPHYSA-N
SMILES OC(=O)C(F)(F)F.CC(C)C[C@H](NC(=O)c1ccc(NCc2c[nH]cn2)cc1-c3cccc4ccccc34)C(O)=O
UNSPSC Code 12352200
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
WGK Germany  WGK 3
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
0
2 0

GGTI 2133 (trifluoroacetate salt) price More Price(9)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich G5294 GGTI-2133 ≥98%(HPLC),solid 1217480-14-2 1mg $227 2026-04-30 Buy
Sigma-Aldrich G5294 GGTI-2133 ≥98%(HPLC),solid 1217480-14-2 5mg $857 2026-04-30 Buy
Cayman Chemical 23418 GGTI 2133 (trifluoroacetate salt) ≥95% 1217480-14-2 500μg $115 2026-04-30 Buy
Cayman Chemical 23418 GGTI 2133 (trifluoroacetate salt) ≥95% 1217480-14-2 1mg $213 2026-04-30 Buy
Biosynth SYB48014 GGTI-2133 1217480-14-2 5mg $1484.95 2026-06-05 Buy
Product number Packaging Price Buy
G5294 1mg $227 Buy
G5294 5mg $857 Buy
23418 500μg $115 Buy
23418 1mg $213 Buy
SYB48014 5mg $1484.95 Buy

GGTI 2133 (trifluoroacetate salt) Chemical Properties, Uses, Production

Description

GGTI 2133 is a peptidomimetic inhibitor of geranylgeranyl transferase type I (GGTase I; IC50 = 38 nM). It is 140-fold selective for GGTase I over farnesyltransferase (IC50 = 5,400 nM). In vitro, it inhibits geranylgeranylation of RAP1A (IC50 = 10 μM) without inhibiting farnesylation of H-Ras (IC50 = >30 μM). It also inhibits cell growth and decreases migration and invasion of oral squamous cell carcinoma (OSSC) cells to 75, 45, and 27% of control values, respectively. GGTI 2133 (5 mg/kg per day, i.p.) prevents ovalbumin-induced eosinophil infiltration into airways in a mouse model of allergic bronchial asthma but does not prevent an increase in chemokines. It also blocks naloxone-induced contraction of ileum isolated from rats with morphine withdrawal syndrome and dose-dependently decreases withdrawal severity in vivo (ED50 = 0.076 mg/kg).

Uses

GGTI-2133 has been used

  • To understand the role of geranylgeranyl transferase in the regulation of CXC chemokine production and neutrophil recruitment in the lung.
  • To study the importance of geranylgeranylation in cell adhesion.
  • To measure ligand-induced ADP-ribosylation factor 6 (Arf6) activation in breast cancer cells.

Biochem/physiol Actions

GGTase I mediates prenylation to induce the oncogenic functions of the Ras and Rho proteins. Thus, GGTase I inhibitors can be utilized as effective anticancer drugs. They are also useful in treating inflammation, atherosclerosis, multiple sclerosis and other diseases.

References

[1] ANIL VASUDEVAN. Potent, Highly Selective, and Non-Thiol Inhibitors of Protein Geranylgeranyltransferase-I[J]. Journal of Medicinal Chemistry, 1999, 42 8: 1333-1340. DOI: 10.1021/jm9900873
[2] MASAKAZU HAMADA. Involvement of RhoA and RalB in geranylgeranyltransferase I inhibitor-mediated inhibition of proliferation and migration of human oral squamous cell carcinoma cells.[J]. Cancer Chemotherapy and Pharmacology, 2011, 68 3: 559-569. DOI: 10.1007/s00280-010-1520-9
[3] Y CHIBA  M M  S Sato. GGTI-2133, an inhibitor of geranylgeranyltransferase, inhibits infiltration of inflammatory cells into airways in mouse experimental asthma.[J]. International Journal of Immunopathology and Pharmacology, 2009, 22 4: 929-935. DOI: 10.1177/039463200902200408
[4] ASHISH K. REHNI  Thakur G S. Pharmacological modulation of geranylgeranyltransferase and farnesyltransferase attenuates opioid withdrawal in vivo and in vitro[J]. Neuropharmacology, 2013, 71: Pages 19-26. DOI: 10.1016/j.neuropharm.2013.01.022

GGTI 2133 (trifluoroacetate salt) Preparation Products And Raw materials

Raw materials

Preparation Products

GGTI 2133 (trifluoroacetate salt) Suppliers

Global Suppliers ( 12)
Supplier Tel Email Country ProdList Advantage
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 9920 65
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51389 80
BOC Sciences 16314854226 info@bocsci.com United States 9909 65
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11963 58
Huai Hua Binfengchem Co., Ltd 0745-2866851 17711757908 3907837691@qq.com China 4745 58
TargetMol Chemicals Inc. 15002134094 marketing@targetmol.cn China 29874 58
GGTI 2133 (trifluoroacetate salt) N-[4-[(1H-imidazol-5-ylmethyl)amino]-2-(1-naphthalenyl)benzoyl]-L-leucine,2,2,2-trifluoroacetatesalt GGTI 2133 TFA 1217480-14-2