Welcome to LookChem.com Sign In|Join Free
  • or
Humantenmine is a synthetic chemical compound that functions as an azole antifungal agent within the pharmaceutical industry. It operates by inhibiting the synthesis of ergosterol, an integral component of the fungal cell membrane, thereby disrupting the cell's structure and function, which results in the death of the fungal cells.

82354-38-9

Post Buying Request

82354-38-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

82354-38-9 Usage

Uses

Used in Pharmaceutical Industry:
Humantenmine is used as an antifungal agent for treating a variety of fungal infections due to its ability to inhibit ergosterol synthesis, which is essential for maintaining fungal cell membrane integrity.
Used in Treatment of Fungal Infections:
Humantenmine is used as a therapeutic agent for conditions such as athlete's foot, ringworm, and vaginal yeast infections, providing relief by targeting and eliminating the fungi causing these infections.
Used in Various Medication Forms:
Humantenmine is utilized in the formulation of creams, ointments, and oral tablets, offering flexibility in treatment administration and catering to different types of fungal infections based on their location and severity.
Used with Caution in Specific Populations:
Humantenmine is used with consideration for potential interactions with other medications and in individuals with certain medical conditions, ensuring safe and effective treatment while minimizing adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 82354-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,5 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82354-38:
(7*8)+(6*2)+(5*3)+(4*5)+(3*4)+(2*3)+(1*8)=129
129 % 10 = 9
So 82354-38-9 is a valid CAS Registry Number.

82354-38-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Humantenmine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82354-38-9 SDS

82354-38-9Downstream Products

82354-38-9Relevant academic research and scientific papers

Divergent Entry to Gelsedine-Type Alkaloids: Total Syntheses of (-)-Gelsedilam, (-)-Gelsenicine, (-)-Gelsedine, and (-)-Gelsemoxonine

Wang, Pingluan,Gao, Yang,Ma, Dawei

supporting information, p. 11608 - 11612 (2018/09/21)

The gelsedine-type alkaloids possess a common oxabicyclo[3.2.2]nonane core and spiro-N-methoxyindolinone moiety along with a diversely functionalized heterocycle embedded in the compact framework. Herein we disclose a divergent entry to gelsedine-type alk

Unified Total Synthesis of Five Gelsedine-Type Alkaloids: (-)-Gelsenicine, (-)-Gelsedine, (-)-Gelsedilam, (-)-14-Hydroxygelsenicine, and (-)-14,15-Dihydroxygelsenicine

Harada, Takaaki,Shimokawa, Jun,Fukuyama, Tohru

, p. 4622 - 4625 (2016/09/28)

The systematic arrangement of a two-carbon unit, hydrogen atom, and oxygen atom on the versatile enal moiety of a non-natural synthetic intermediate successfully led to the unified access to the gelsedine-type alkaloids. The development and use of this ne

Spectroscopic analyses and chemical transformation for structure elucidation of two novel indole alkaloids from Gelsemium elegans

Yamada, Yousuke,Kitajima, Mariko,Kogure, Noriyuki,Wongseripipatana, Sumphan,Takayama, Hiromitsu

body text, p. 3341 - 3344 (2009/09/05)

Two new monoterpenoid oxindole alkaloids, gelsevanillidine (1) having an additional vanillin residue on gelsenicine-type alkaloid and gelseoxazolidinine (2) possessing an unusual oxazolidine ring, were isolated from Gelsemium elegans. To confirm their str

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 82354-38-9