Sanjay Adhikary
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Graduate Assistant
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Sanjay Adhikary's research focuses on the investigation of potential therapeutic agents, particularly in the context of melanoma treatment. His work includes exploring the antimicrobial properties of plant extracts, such as those from Verbena officinalis. Adhikary has also synthesized and studied novel thiazole-fused bisnoralcohol derivatives and thiazole-fused androstenone and ethisterone derivatives, identifying them as potent inhibitors of the β- and γ-actin cytoskeleton, which may be relevant for treating melanoma tumors. His recent publications also touch upon the role of ATF6 activation in promoting immune checkpoint blockade (ICB) response in melanoma. Adhikary has collaborated with researchers from Arkansas State University and the University of Arkansas for Medical Sciences on multiple publications. His scholarship metrics include an h-index of 2, with 9 total publications and 12 total citations.
Metrics
- h-index: 2
- Publications: 9
- Citations: 12
Positions
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Graduate Assistant publications 2025–2026University of Arkansas for Medical Sciences Institution web page
Selected Publications
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Abstract 6545: Characterizing ATF6 activation-driven mechanisms improving ICB efficacy (2026)
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691 ATF6 activation promotes ICB response in melanoma (2025)
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Correction: Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors (2025)
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Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors (2024)
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Efficient Synthesis of Thiazole-Fused Bisnoralcohol Derivatives as Potential Therapeutic Agents (2024)
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In Vitro Antimelanoma Properties of Verbena officinalis Fractions (2022)
Collaboration Network
Top Collaborators
- In Vitro Antimelanoma Properties of Verbena officinalis Fractions
- Efficient Synthesis of Thiazole-Fused Bisnoralcohol Derivatives as Potential Therapeutic Agents
- Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Correction: Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Correction: Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- 691 ATF6 activation promotes ICB response in melanoma
- Abstract 6545: Characterizing ATF6 activation-driven mechanisms improving ICB efficacy
- Efficient Synthesis of Thiazole-Fused Bisnoralcohol Derivatives as Potential Therapeutic Agents
- Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Correction: Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Correction: Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Abstract 6545: Characterizing ATF6 activation-driven mechanisms improving ICB efficacy
- Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Correction: Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Correction: Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- Correction: Thiazole-fused androstenone and ethisterone derivatives: potent β- and γ-actin cytoskeleton inhibitors to treat melanoma tumors
- 691 ATF6 activation promotes ICB response in melanoma
- Abstract 6545: Characterizing ATF6 activation-driven mechanisms improving ICB efficacy
- 691 ATF6 activation promotes ICB response in melanoma
- Abstract 6545: Characterizing ATF6 activation-driven mechanisms improving ICB efficacy
- 691 ATF6 activation promotes ICB response in melanoma
- Abstract 6545: Characterizing ATF6 activation-driven mechanisms improving ICB efficacy
- 691 ATF6 activation promotes ICB response in melanoma
- Abstract 6545: Characterizing ATF6 activation-driven mechanisms improving ICB efficacy
- 691 ATF6 activation promotes ICB response in melanoma
- Abstract 6545: Characterizing ATF6 activation-driven mechanisms improving ICB efficacy
- 691 ATF6 activation promotes ICB response in melanoma
- Abstract 6545: Characterizing ATF6 activation-driven mechanisms improving ICB efficacy
- In Vitro Antimelanoma Properties of Verbena officinalis Fractions
- In Vitro Antimelanoma Properties of Verbena officinalis Fractions
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