Cas no 90365-56-3 ((+)-Indolactam V)

(+)-Indolactam V is a biologically active indole alkaloid known for its role as a potent protein kinase C (PKC) activator. This compound is particularly valued in biochemical and pharmacological research for its ability to selectively modulate PKC signaling pathways, making it a useful tool for studying cell regulation, differentiation, and tumor promotion mechanisms. Its high purity and well-defined stereochemistry ensure reliable and reproducible experimental results. (+)-Indolactam V is commonly employed in studies exploring cancer biology, neurobiology, and signal transduction, offering researchers a precise means to investigate PKC-mediated processes. Its stability and specificity make it a preferred choice for in vitro and cellular assays.
(+)-Indolactam V structure
(+)-Indolactam V structure
Product Name:(+)-Indolactam V
CAS No:90365-56-3
MF:C17H23N3O2
MW:301.383424043655
CID:798295
PubChem ID:1288
Update Time:2025-06-28

(+)-Indolactam V Chemical and Physical Properties

Names and Identifiers

    • 3H-Pyrrolo[4,3,2-gh]-1,4-benzodiazonin-3-one,1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-, (2R,5R)-(9CI)
    • (+)-Indolactam V
    • 3H-Pyrrolo[4,3,2-gh]-1,4-benzodiazonin-3-one,1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-...
    • 3H-Pyrrolo[4,3,2-gh]-1,4-benzodiazonin-3-one,1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-, (2R,5R)-(9C
    • NSC_105000
    • (10S,13S)-13-(hydroxymethyl)-9-methyl-10-propan-2-yl-3,9,12-triazatricyclo[6.6.1.0^{4,15]pentadeca-1,4(15),5,7-tetraen-11-one
    • BDBM86430
    • SMP2_000017
    • 90365-56-3
    • (-)-Indolactam V (low PS)
    • CAS_105000
    • Inchi： 1S/C17H23N3O2/c1-10(2)16-17(22)19-12(9-21)7-11-8-18-13-5-4-6-14(15(11)13)20(16)3/h4-6,8,10,12,16,18,21H,7,9H2,1-3H3,(H,19,22)
    • InChI Key： LUZOFMGZMUZSSK-UHFFFAOYSA-N
    • SMILES： O=C1C(C(C)C)N(C)C2C=CC=C3C=2C(=CN3)CC(CO)N1

Computed Properties

  • Exact Mass: 301.179
  • Monoisotopic Mass: 301.179
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 22
  • Rotatable Bond Count: 2
  • Complexity: 415
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 2
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: 3
  • XLogP3: 2.3
  • Topological Polar Surface Area: 68.4?2

Experimental Properties

  • Color/Form: Not available
  • Density: 1.166
  • Boiling Point: 584°C at 760 mmHg
  • Flash Point: 307°C
  • Refractive Index: 1.589
  • Solubility: Not available

(+)-Indolactam V Security Information

  • Hazard Category Code： 36/37/38
  • Safety Instruction： 26-36
  • Hazardous Material Identification： Xi
  • Storage Condition：-20°C

(+)-Indolactam V Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
I577423-2.5mg
(+)-Indolactam V
 90365-56-3
2.5mg
 $1613.00 2023-05-18
TRC
I577423-5mg
(+)-Indolactam V
 90365-56-3
5mg
 $3003.00 2023-05-18
TRC
I577423-10mg
(+)-Indolactam V
 90365-56-3
10mg
 $5465.00 2023-05-18
SHENG KE LU SI SHENG WU JI SHU
sc-203085-300 μg
(+)-Indolactam V,
 90365-56-3
300μg
 ￥827.00 2023-07-10
TRC
I577423-25mg
(+)-Indolactam V
 90365-56-3
25mg
 $ 19000.00 2023-09-07
SHENG KE LU SI SHENG WU JI SHU
sc-203085-300μg
(+)-Indolactam V,
 90365-56-3
300μg
 ￥827.00 2023-09-05

(+)-Indolactam V Related Literature

Related Categories

Additional information on (+)-Indolactam V

(+)-Indolactam V: A Comprehensive Overview

Introduction to (+)-Indolactam V

(+)-Indolactam V, a compound with the CAS number 90365-56-3, is a fascinating molecule that has garnered significant attention in the fields of organic chemistry and pharmacology. This compound, belonging to the indole alkaloid family, is characterized by its unique structure and intriguing biological properties. Recent studies have shed light on its potential applications in drug discovery, particularly in the development of novel therapeutic agents.

Structural Features and Synthesis

The structure of (+)-Indolactam V is notable for its indole ring fused with a lactam group, which contributes to its distinctive chemical properties. The compound's synthesis has been a topic of extensive research, with chemists developing innovative strategies to efficiently synthesize this molecule. For instance, recent advancements in catalytic asymmetric synthesis have enabled the preparation of enantiomerically pure (+)-Indolactam V, which is crucial for studying its stereochemical effects on biological activity.

Biological Activity and Applications

One of the most compelling aspects of (+)-Indolactam V is its diverse biological activity. Studies have demonstrated that this compound exhibits potent anti-tumor properties, making it a promising candidate for cancer therapy. Additionally, research has shown that (+)-Indolactam V possesses anti-inflammatory and antioxidant effects, which could be harnessed for treating chronic diseases such as neurodegenerative disorders.

Recent investigations have also explored the potential of (+)-Indolactam V as an antiviral agent. Its ability to inhibit viral replication mechanisms suggests that it could be developed into a novel class of antiviral drugs. These findings underscore the importance of further research into the pharmacological profile of (+)-Indolactam V, particularly in preclinical models.

Current Research Trends and Future Directions

The scientific community continues to explore new avenues for understanding the mechanisms underlying the biological activity of (+)-Indolactam V. Cutting-edge techniques such as X-ray crystallography and molecular docking are being employed to elucidate how this compound interacts with cellular targets at the molecular level.

Moreover, there is growing interest in leveraging (+)-Indolactam V as a lead compound for drug design. Researchers are investigating ways to modify its structure to enhance bioavailability and efficacy while minimizing potential side effects. These efforts are expected to pave the way for the development of next-generation therapeutics based on this intriguing molecule.

In conclusion, (+)-Indolactam V (CAS No. 90365-56-3) stands out as a remarkable compound with immense potential in various therapeutic areas. As research progresses, it is anticipated that this molecule will continue to contribute significantly to advancements in medicinal chemistry and pharmacology.

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