253863-00-2,MFCD09970379
Catalog No.:AA003R47

253863-00-2 | L-778123 hydrochloride

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5mg
≥98%
in stock  
$139.00   $97.00
- +
10mg
≥98%
in stock  
$236.00   $165.00
- +
25mg
≥98%
in stock  
$550.00   $385.00
- +
50mg
≥98%
in stock  
$960.00   $672.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003R47
Chemical Name:
L-778123 hydrochloride
CAS Number:
253863-00-2
Molecular Formula:
C22H21Cl2N5O
Molecular Weight:
442.3410
MDL Number:
MFCD09970379
SMILES:
N#Cc1ccc(cc1)Cn1cncc1CN1CCN(C(=O)C1)c1cccc(c1)Cl.Cl
Properties
Properties
 
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
614  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
30  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Literature

Title: Modulation of anthracycline-induced cytotoxicity by targeting the prenylated proteome in myeloid leukemia cells.

Journal: Journal of molecular medicine (Berlin, Germany) 20120201

Title: ErbB-2 blockade and prenyltransferase inhibition alter epidermal growth factor and epidermal growth factor receptor trafficking and enhance (111)In-DTPA-hEGF Auger electron radiation therapy.

Journal: Journal of nuclear medicine : official publication, Society of Nuclear Medicine 20110501

Title: A tagging-via-substrate approach to detect the farnesylated proteome using two-dimensional electrophoresis coupled with Western blotting.

Journal: Molecular & cellular proteomics : MCP 20100401

Title: Development of farnesyl transferase inhibitors: a review.

Journal: The oncologist 20050901

Title: Isoprenylation of intracellular proteins as a new target for the therapy of human neoplasms: preclinical and clinical implications.

Journal: Current drug targets 20050501

Title: [Farnesyltransferase inhibitors: preliminary results in acute myeloid leukemia].

Journal: Bulletin du cancer 20050301

Title: Inhibition of lymphocyte activation and function by the prenylation inhibitor L-778,123.

Journal: Investigational new drugs 20050101

Title: Crystallographic analysis reveals that anticancer clinical candidate L-778,123 inhibits protein farnesyltransferase and geranylgeranyltransferase-I by different binding modes.

Journal: Biochemistry 20040720

Title: Farnesyl transferase inhibitors for patients with lung cancer.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20040615

Title: [Ras signaling pathway as a target for farnesyltransferase inhibitors--a new, promising prospects in the treatment for malignant disorders].

Journal: Wiadomosci lekarskie (Warsaw, Poland : 1960) 20040101

Title: Farnesyltransferase inhibitors are potent lung cancer chemopreventive agents in A/J mice with a dominant-negative p53 and/or heterozygous deletion of Ink4a/Arf.

Journal: Oncogene 20030918

Title: Farnesyltransferase inhibitors as radiation sensitizers.

Journal: International journal of radiation biology 20030701

Title: Farnesyl transferase inhibitors in the treatment of breast cancer.

Journal: Expert opinion on investigational drugs 20030301

Title: The effects of the farnesyl transferase inhibitor FTI L-778,123 on normal, myelodysplastic, and myeloid leukemia bone marrow progenitor proliferation in vitro.

Journal: Leukemia & lymphoma 20030101

Title: Farnesyl transferase inhibitors as anticancer agents.

Journal: European journal of cancer (Oxford, England : 1990) 20020901

Title: A phase I and pharmacological study of the farnesyl protein transferase inhibitor L-778,123 in patients with solid malignancies.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20011201

Title: Ras inhibitors and radiation therapy.

Journal: Seminars in radiation oncology 20011001

Title: Farnesyltransferase inhibitors.

Journal: Seminars in oncology 20011001

Title: Anions modulate the potency of geranylgeranyl-protein transferase I inhibitors.

Journal: The Journal of biological chemistry 20010706

Title: High-performance liquid chromatography/mass spectrometry characterization of Ki4B-Ras in PSN-1 cells treated with the prenyltransferase inhibitor L-778,123.

Journal: Analytical biochemistry 20010301

Title: Lobell RB, et al. Preclinical and clinical pharmacodynamic assessment of L-778,123, a dual inhibitor of farnesyl:protein transferase and geranylgeranyl:protein transferase type-I. Mol Cancer Ther. 2002 Jul;1(9):747-758.

Title: Ghasemi S, et al. Comparison of Cytotoxic Activity of L778123 as a Farnesyltranferase Inhibitor and Doxorubicin against A549 and HT-29 Cell Lines. Adv Pharm Bull. 2013;3(1):73-77.

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Related Products of 253863-00-2
Tags:253863-00-2 Molecular Formula|253863-00-2 MDL|253863-00-2 SMILES|253863-00-2 L-778123 hydrochloride
Catalog No.: AA003R47
253863-00-2,MFCD09970379
253863-00-2 | L-778123 hydrochloride
Pack Size: 5mg
Purity: ≥98%
in stock
$139.00 $97.00
Pack Size: 10mg
Purity: ≥98%
in stock
$236.00 $165.00
Pack Size: 25mg
Purity: ≥98%
in stock
$550.00 $385.00
Pack Size: 50mg
Purity: ≥98%
in stock
$960.00 $672.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA003R47
Chemical Name: L-778123 hydrochloride
CAS Number: 253863-00-2
Molecular Formula: C22H21Cl2N5O
Molecular Weight: 442.3410
MDL Number: MFCD09970379
SMILES: N#Cc1ccc(cc1)Cn1cncc1CN1CCN(C(=O)C1)c1cccc(c1)Cl.Cl
Properties
Storage: Inert atmosphere;2-8℃;  
Complexity: 614  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 30  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
Literature fold

Title: Modulation of anthracycline-induced cytotoxicity by targeting the prenylated proteome in myeloid leukemia cells.

Journal: Journal of molecular medicine (Berlin, Germany)20120201

Title: ErbB-2 blockade and prenyltransferase inhibition alter epidermal growth factor and epidermal growth factor receptor trafficking and enhance (111)In-DTPA-hEGF Auger electron radiation therapy.

Journal: Journal of nuclear medicine : official publication, Society of Nuclear Medicine20110501

Title: A tagging-via-substrate approach to detect the farnesylated proteome using two-dimensional electrophoresis coupled with Western blotting.

Journal: Molecular & cellular proteomics : MCP20100401

Title: Development of farnesyl transferase inhibitors: a review.

Journal: The oncologist20050901

Title: Isoprenylation of intracellular proteins as a new target for the therapy of human neoplasms: preclinical and clinical implications.

Journal: Current drug targets20050501

Title: [Farnesyltransferase inhibitors: preliminary results in acute myeloid leukemia].

Journal: Bulletin du cancer20050301

Title: Inhibition of lymphocyte activation and function by the prenylation inhibitor L-778,123.

Journal: Investigational new drugs20050101

Title: Crystallographic analysis reveals that anticancer clinical candidate L-778,123 inhibits protein farnesyltransferase and geranylgeranyltransferase-I by different binding modes.

Journal: Biochemistry20040720

Title: Farnesyl transferase inhibitors for patients with lung cancer.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research20040615

Title: [Ras signaling pathway as a target for farnesyltransferase inhibitors--a new, promising prospects in the treatment for malignant disorders].

Journal: Wiadomosci lekarskie (Warsaw, Poland : 1960)20040101

Title: Farnesyltransferase inhibitors are potent lung cancer chemopreventive agents in A/J mice with a dominant-negative p53 and/or heterozygous deletion of Ink4a/Arf.

Journal: Oncogene20030918

Title: Farnesyltransferase inhibitors as radiation sensitizers.

Journal: International journal of radiation biology20030701

Title: Farnesyl transferase inhibitors in the treatment of breast cancer.

Journal: Expert opinion on investigational drugs20030301

Title: The effects of the farnesyl transferase inhibitor FTI L-778,123 on normal, myelodysplastic, and myeloid leukemia bone marrow progenitor proliferation in vitro.

Journal: Leukemia & lymphoma20030101

Title: Farnesyl transferase inhibitors as anticancer agents.

Journal: European journal of cancer (Oxford, England : 1990)20020901

Title: A phase I and pharmacological study of the farnesyl protein transferase inhibitor L-778,123 in patients with solid malignancies.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research20011201

Title: Ras inhibitors and radiation therapy.

Journal: Seminars in radiation oncology20011001

Title: Farnesyltransferase inhibitors.

Journal: Seminars in oncology20011001

Title: Anions modulate the potency of geranylgeranyl-protein transferase I inhibitors.

Journal: The Journal of biological chemistry20010706

Title: High-performance liquid chromatography/mass spectrometry characterization of Ki4B-Ras in PSN-1 cells treated with the prenyltransferase inhibitor L-778,123.

Journal: Analytical biochemistry20010301

Title: Lobell RB, et al. Preclinical and clinical pharmacodynamic assessment of L-778,123, a dual inhibitor of farnesyl:protein transferase and geranylgeranyl:protein transferase type-I. Mol Cancer Ther. 2002 Jul;1(9):747-758.

Title: Ghasemi S, et al. Comparison of Cytotoxic Activity of L778123 as a Farnesyltranferase Inhibitor and Doxorubicin against A549 and HT-29 Cell Lines. Adv Pharm Bull. 2013;3(1):73-77.

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