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Isotretinoin (13-cis retinoic acid) Hydroxylase activator

Cat.No.S1379

Isotretinoin (13-cis retinoic acid) was developed as a chemotherapy medication for the treatment of brain cancer, pancreatic cancer and more.
Isotretinoin (13-cis retinoic acid) Hydroxylase activator Chemical Structure

Chemical Structure

Molecular Weight: 300.44

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Quality Control

Batch: Purity: 99.97%
99.97

Solubility

In vitro
Batch:

DMSO : 60 mg/mL (199.7 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

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In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO
%
% Tween 80
% ddH2O
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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Chemical Information, Storage & Stability

Molecular Weight 300.44 Formula

C20H28O2

Storage (From the date of receipt)
CAS No. 4759-48-2 Download SDF Storage of Stock Solutions

Mechanism of Action

Targets/IC50/Ki
hydroxylase
In vitro
Isotretinoin (13-cis retinoic acid) directly interferes with the development of cranial neural crest cells. This compound selectively affects neural crest cells by decreasing their cell-substratum adhesion.
In vivo
Isotretinoin (13-cis retinoic acid) (500 ng/mL) and its main metabolite in the human, 4-oxo-isotretinoin, induce malformations similar to those seen in vivo. It impairs explicit memory in Stage 2, but retention tests one month after exposure ended, indicated recovery from this explicit memory impairment and evidence of enhanced implicit memory in the 10 mg and 15 mg ISO rats. This compound slows the recovery of rod signaling after exposure to an intense bleaching light, and that rhodopsin regeneration is markedly slowed. It is also found to protect rat photoreceptors from light-induced damage. Isotretinoin blocks the formation of A2E biochemically and the accumulation of lipofuscin pigments by electron microscopy. It also blocks the slower, age-dependent accumulation of lipofuscin in wild-type mice.
References
  • [4] https://pubmed.ncbi.nlm.nih.gov/11172037/
  • [5] https://pubmed.ncbi.nlm.nih.gov/12671074/

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06225570 Not yet recruiting
Acne Vulgaris
Medical University of South Carolina
January 2025 Early Phase 1
NCT05316675 Not yet recruiting
Acne Vulgaris
Assiut University
December 2022 Phase 4
NCT03939364 Withdrawn
Leukoplakia Oral
Skyline Biosciences
January 2022 Phase 1
NCT05218486 Active not recruiting
Acne Vulgaris
Alshimaa Abbas Mohamed Ebrahim|Aswan University
August 1 2021 Phase 4

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