Details
Stereochemistry | ACHIRAL |
Molecular Formula | C2H4Cl3O2Te.H4N |
Molecular Weight | 312.05 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[NH4+].Cl[Te-]1(Cl)(Cl)OCCO1
InChI
InChIKey=AXWLPMGUUAIGJK-UHFFFAOYSA-O
InChI=1S/C2H4Cl3O2Te.H3N/c3-8(4,5)6-1-2-7-8;/h1-2H2;1H3/q-1;/p+1
Molecular Formula | C2H4Cl3O2Te |
Molecular Weight | 294.01 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | H3N |
Molecular Weight | 17.0305 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Ammonium trichlorotellurate (AS-101) is a synthetic non-toxic tellurium derivative, structurally similar to cisplatin, with immunostimulatory and anti-hair loss properties. Ammonium trichlorotellurate induces production of colony stimulating factor (CSF), interleukin-2 (IL-2), and IL-2 receptors by increasing the calcium ion influx through the cell membrane and subsequently exerts its immunostimulatory effects through the CSF-mediated increase in macrophage/granulocytes. This agent is also a potent inducer of interferon and a spectrum of cytokines such as IL-1, IL-6, and tumor necrosis factor (TNF). In animal studies, ammonium trichlorotellurate exerts its anti-hair loss effect by inducing anagen and obstructing spontaneous catagen via promoting follicular keratinocyte proliferation and interfering with terminal differentiation, respectively. AS-101 suppresses production of HIV-1. It inhibited reverse transcriptase activity and replication of human immunodeficiency virus type 1. RDDP and DDDP activities were impaired by the drug with calculated IC50 value of about 4 uM. Intravenous AS-101 was in trials in patients with HIV infections. AS-101, a small-molecule integrin αvβ3 and VLA-4 inhibitor is being developed by BioMAS in Israel for the treatment of genital warts, age-related macular degeneration and fertility preservation. Phase II clinical trials are ongoing. The drug was also undergoing phase II development in acute myeloid leukaemia, atopic dermatitis, chemotherapy-induced damage, myelodysplastic syndromes, thrombocytopenia, alopecia, psoriasis. However, development for these indications was discontinued.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT01555112
15% AS-101 ointment applied twice a day for treatment of external genital warts.
Route of Administration:
Topical
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28326083
Isolated rat glomerular macrophages were cultured with SAC (5 ug/ml) for 24 h. Cells were detached and cultured at 104/well in triplicates in the presence or absence of various AS-101 concentrations (0.05-1 ug/ml) for 1 h. Caspase-1 activity was evaluated. AS-101 significantly inhibited Caspase-1 activity in a dose-dependent manner.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:39:44 GMT 2023
by
admin
on
Fri Dec 15 15:39:44 GMT 2023
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Record UNII |
708681952A
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Record Status |
Validated (UNII)
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Record Version |
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FDA ORPHAN DRUG |
22387
Created by
admin on Fri Dec 15 15:39:44 GMT 2023 , Edited by admin on Fri Dec 15 15:39:44 GMT 2023
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NCI_THESAURUS |
C2139
Created by
admin on Fri Dec 15 15:39:44 GMT 2023 , Edited by admin on Fri Dec 15 15:39:44 GMT 2023
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106566-58-9
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C1006
Created by
admin on Fri Dec 15 15:39:44 GMT 2023 , Edited by admin on Fri Dec 15 15:39:44 GMT 2023
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708681952A
Created by
admin on Fri Dec 15 15:39:44 GMT 2023 , Edited by admin on Fri Dec 15 15:39:44 GMT 2023
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PRIMARY |