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Details

Stereochemistry ACHIRAL
Molecular Formula AsI3
Molecular Weight 455.635
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ARSENIC TRIIODIDE

SMILES

I[As](I)I

InChI

InChIKey=IKIBSPLDJGAHPX-UHFFFAOYSA-N
InChI=1S/AsI3/c2-1(3)4

HIDE SMILES / InChI

Molecular Formula AsI3
Molecular Weight 455.635
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Arsenic trioxide (ATO) is used to treat acute promyelocytic leukemia in people who have not been helped by other types of chemotherapy or whose condition has improved but then worsened following treatment with other types of chemotherapy. Arsenic trioxide acts through activation of Jun N-terminal kinase (JNK), activator protein-1, and inhibition of dual-specificity phosphatases. Although the exact mechanisms under which ATO exerts its therapeutic effect in acute promyelocytic leukemia cancer cells are not well elucidated. It was shown that apoptotic mechanisms involved the induction of phosphatidylserine externalization, caspase-3 activation, and nucleosomal DNA fragmentation. Adverse reactions described are leukocytosis, nausea, vomiting, diarrhea, and abdominal pain, fatigue, edema, hyperglycemia, dyspnea, cough, rash or itching, headaches, and dizziness.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: dual-specificity phosphatases
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
TRISENOX

Approved Use

Acute promyelocytic leukemia (newly diagnosed) (low-risk disease): Treatment of newly diagnosed low-risk acute promyelocytic leukemia (APL), in combination with tretinoin, in adults whose APL is characterized by the presence of the t(15;17) translocation or PML/RAR-alpha gene expression Acute promyelocytic leukemia (relapsed or refractory): Remission induction and consolidation treatment of APL in patients who are refractory to, or have relapsed from, retinoid and anthracycline chemotherapy, and whose APL is characterized by the presence of the t(15;17) translocation or PML/RAR-alpha gene expression

Launch Date

9.6984E11

Sample Use Guides

Induction Treatment Schedule: TRISENOX™ should be administered intravenously at a dose of 0.15 mg/kg daily until bone marrow remission. Total induction dose should not exceed 60 doses. Consolidation Treatment Schedule: Consolidation treatment should begin 3 to 6 weeks after completion of induction therapy. TRISENOX™ should be administered intravenously at a dose of 0.15 mg/kg daily for 25 doses over a period up to 5 weeks.
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:24:43 UTC 2023
Edited
by admin
on Fri Dec 15 17:24:43 UTC 2023
Record UNII
3029988O2T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ARSENIC TRIIODIDE
HSDB   MART.   MI   WHO-DD  
Systematic Name English
TRIIODOARSINE
Systematic Name English
ARSENIC TRIIODIDE [HSDB]
Common Name English
ARSENIC TRIIODIDE [MART.]
Common Name English
ARSENICUM IODATUM
HPUS  
Common Name English
Arsenic triiodide [WHO-DD]
Common Name English
ARSENIC TRIIODIDE [MI]
Common Name English
ARSENOUS TRIIODIDE
Systematic Name English
ARSENICUM IODATUM [HPUS]
Common Name English
ARSENIC (III) IODIDE
Systematic Name English
Code System Code Type Description
WIKIPEDIA
ARSENIC TRIIODIDE
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
EVMPD
SUB71543
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
EPA CompTox
DTXSID9064843
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
DAILYMED
3029988O2T
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
SMS_ID
100000135621
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
CAS
7784-45-4
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
ECHA (EC/EINECS)
232-068-4
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
FDA UNII
3029988O2T
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
PUBCHEM
24575
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
HSDB
420
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
MESH
C530601
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY
MERCK INDEX
m2064
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY Merck Index
RXCUI
1309691
Created by admin on Fri Dec 15 17:24:43 UTC 2023 , Edited by admin on Fri Dec 15 17:24:43 UTC 2023
PRIMARY RxNorm
Related Record Type Details
ACTIVE MOIETY