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Home > Biochemical Engineering > Plant Extracts > Irinotecan hydrochloride for Sale > Best Seller of Irinotecan hydrochloride CAS NO (100286-90-6) At Best Selling Price
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Best Seller of Irinotecan hydrochloride CAS NO (100286-90-6) At Best Selling Price

Unit Price: Get Latest Price
CAS No.:

100286-90-6

Grade:

Industrial Grade

Content:

99%

Port:

Durban

Brand:

Custom

Packaging:

As per customer requirement

Price valid (until):

2024-05-30

Company Type:
Distributor
Location:
South Africa
Qualification:
Main Products:

Sodium Lauryl Ether Sulfate,Caustic Soda,Soda Ash,Citric Acid,Calcium Hypochlorite,Oxalic Acid

  • Product Description

  • Seller Information

  • Description


      Product Detail  


                                                                                        1. Title: Guanine (73-40-5): Structure, Functions, and Biological Significance

                                                                                          1. Introduction to Guanine (73-40-5)

                                                                                            • Guanine is a vital nitrogenous base found in nucleic acids, playing essential roles in various biological processes.
                                                                                            • This review aims to explore the structure, functions, and biological significance of guanine in living organisms.
                                                                                          2. Chemical Structure and Properties

                                                                                            • Guanine is a heterocyclic organic compound belonging to the purine group, consisting of fused pyrimidine and imidazole rings.
                                                                                            • It is a colorless, crystalline solid with a melting point of approximately 360°C and is sparingly soluble in water.
                                                                                          3. Role in Nucleic Acids

                                                                                            • Guanine is one of the four nucleobases found in DNA and RNA, where it pairs with cytosine through three hydrogen bonds in DNA or with uracil in RNA.
                                                                                            • It forms complementary base pairs with cytosine, contributing to the stability and fidelity of the genetic code.
                                                                                          4. Genetic Code and Protein Synthesis

                                                                                            • In DNA, guanine pairs with cytosine, forming two hydrogen bonds, and participates in the storage and transmission of genetic information.
                                                                                            • During protein synthesis, guanine-containing codons in mRNA specify the incorporation of specific amino acids into polypeptide chains, contributing to the synthesis of proteins.
                                                                                          5. Biological Functions

                                                                                            • Guanine plays crucial roles in various physiological processes, including DNA replication, repair, and transcription, as well as RNA processing and translation.
                                                                                            • It serves as a substrate for enzymes involved in nucleic acid metabolism, such as DNA polymerases, RNA polymerases, and ribonucleases.
                                                                                          6. Energy Metabolism

                                                                                            • Guanine derivatives, such as guanosine triphosphate (GTP) and guanosine diphosphate (GDP), serve as high-energy intermediates in cellular energy metabolism.
                                                                                            • GTP acts as a donor of phosphate groups in phosphorylation reactions and serves as a cofactor for GTP-binding proteins involved in signal transduction pathways.
                                                                                          7. Biomedical Applications

                                                                                            • Guanine and its derivatives have biomedical applications in the fields of molecular biology, genetics, and medicine.
                                                                                            • They are used as molecular probes, fluorescent dyes, and therapeutic agents targeting nucleic acid-based processes and signaling pathways.
                                                                                          8. Disease Associations

                                                                                            • Mutations in genes encoding enzymes involved in guanine metabolism are associated with various genetic disorders, including Lesch-Nyhan syndrome and familial dysautonomia.
                                                                                            • Aberrant guanine metabolism is implicated in carcinogenesis, neurodegeneration, and other pathological conditions.
                                                                                          9. Drug Targets and Therapeutic Strategies

                                                                                            • Guanine-based compounds serve as targets for chemotherapy agents and antiviral drugs that interfere with nucleic acid synthesis and replication in cancer cells and viruses.
                                                                                            • Targeting guanine metabolism represents a promising approach for the development of novel therapeutics for cancer, infectious diseases, and genetic disorders.
                                                                                          10. Conclusion: Importance of Guanine in Biology and Medicine

                                                                                            • Guanine plays essential roles in nucleic acid structure, genetic information, and cellular metabolism, making it a fundamental molecule in biology and medicine.
                                                                                            • Understanding the structure, functions, and regulation of guanine metabolism provides insights into the molecular basis of health and disease, paving the way for the development of innovative diagnostic and therapeutic interventions.







      Specifications  


    Items Specifications
    CAS Number 73-40-5
    Chemical Formula C5H5N5O
    Molecular Weight Approximately 151.13 g/mol
    Appearance White to off-white crystalline powder
    Purity ≥ 98%
    Melting Point 300-302°C
    Boiling Point Decomposes above 300°C
    Density 1.585 g/cm³
    Solubility Slightly soluble in water, insoluble in organic solvents
    Storage Store in a cool, dry place away from heat and moisture
    Stability Stable under normal conditions
    Odor Odorless
    Applications Used in the synthesis of nucleic acids, cosmetics, and pharmaceuticals





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    Basic Info
    Product Name:

    Irinotecan hydrochloride

    Other Name:

    [1,4′-Bipiperidine]-1′-carboxylic acid,(4S)-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-1H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinolin-9-yl ester,hydrochloride (1:1);[1,4′-Bipiperidine]-1′-carboxylic acid,4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-1H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinolin-9-yl ester,monohydrochloride,(S)-;[1,4′-Bipiperidine]-1′-carboxylic acid,(4S)-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-1H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinolin-9-yl ester,monohydrochloride;1H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline,[1,4′-bipiperidine]-1′-carboxylic acid deriv.;CPT 11;Camptothecin 11;7-Ethyl-10-[[4-(1-piperidyl)-1-piperidyl]carbonyloxy]camptothecin hydrochloride;Camptothecin 11 hydrochloride;Irinotecan hydrochloride;U 101440E;Topotecin;Campto;Camptosar;Topotesin;(19S)-10,19-Diethyl-19-hydroxy-14,18-dioxo-17-oxa-3,13-diazapentacyclo[11.8.0.0[2,11].0[4,9].0[15,20]]henicosa-1(21),2(11),3,5,7,9,15(20)-heptaen-7-yl 4-(piperidin-1-yl)piperidine-1-carboxylate hydrochloride;111348-33-5

    CAS No.:

    100286-90-6

    Molecular Formula:

    C33H38N4O6.ClH

    InChIKeys:

    InChIKey=GURKHSYORGJETM-WAQYZQTGSA-N

    Molecular Weight:

    623.14

    Exact Mass:

    622.255798

    EC Number:

    1308068-626-2

    UNII:

    06X131E4OE

    NSC Number:

    759878|616348

    DSSTox ID:

    DTXSID6045953

    HScode:

    29399990

    Categories:

    Plant Extracts

    Characteristics
    PSA:

    113

    XLogP3:

    4.76890

    Appearance:

    Yellow crystalline powder

    Melting Point:

    250-256°C (dec.)

    Boiling Point:

    257 °C

    Flash Point:

    482ºC

    Refractive Index:

    67.7 ° (C=1, H2O)

    Water Solubility:

    soluble in DMSO at 100mg/ml. soluble in water at 25mg/ml with warming;soluble in DMF at approximately 20mg/ml. Sparingly soluble in aqueous buffers.

    Storage Conditions:

    Refrigerator

    Vapor Pressure:

    1.31E-32mmHg at 25°C

    Hazard Identification

    Classification of the substance or mixture

    Acute toxicity - Category 4, Oral

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Warning

    Hazard statement(s)

    H302 Harmful if swallowed

    Precautionary statement(s)
    Prevention

    P264 Wash ... thoroughly after handling.

    P270 Do not eat, drink or smoke when using this product.

    Response

    P301+P317 IF SWALLOWED: Get medical help.

    P330 Rinse mouth.

    Storage

    none

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Distributor

    Main Products:

    Sodium Lauryl Ether Sulfate,Caustic Soda,Soda Ash,Citric Acid,Calcium Hypochlorite,Oxalic Acid

    Location:

    13 PROTEA PARK MILKWOOD STREET RANGEVIEW GAUTENG 1739

    Payment Terms:

    TT against copy of documents,TT against B/L draft before shipment

    Average lead Time:

    60

    Total Annual Revenue:

    $1 million-$2.5 million

    Total Employees:

    11-50

    Year of Establishment:

    2012

  • Country Product Purchase Quantity Date Posted
    Post an enquiry for this product
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