MHG Molecules.fun

Real World Use of Blockchain for Social Good and Science advancement

Tokenizing Drug Development to accelerate and enable IP to reach the market.

Enabling Decentralized Innovation

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Problem Statement

Drug development is slow, expensive, and centralized.

Small molecule IP that never makes it to market. Orphan indications underserved. Misallocation of capital - inefficiency & misalignment of incentives. Decentralized inventors limited access to resources. Weak incentives for collaboration.

Our Vision

A decentralized ecosystem where small molecules are tokenized, allowing transparent funding, collaboration, and fair value distribution. Enabling rapid development and new solutions which improve healthcare and lives of people.

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Platform Overview

Small Molecules IP is tokenized.

Focussed teams & Partners drive clinical development stages. Token holders share in the upside - clinical value inflections and IP commercialization.

Platform Overview
Development Oracle

Development Oracle

Each drug passes through stages:

Oracle evaluates stage & value. 10% locked tokens fund validation.

  • Wet Lab / Pre-Clinical
  • Clinical Phase I Study
  • Clinical Phase II Study
  • Clinical Phase III Study
  • Manufacturing / Distribution

Value to Token Holders

Each molecule company (SPV) is legally bonded to:

  • Allocate 30% of lifecycle value
  • Buy back & burn tokens
  • Linear, ongoing approach
Tokenomics

Transparent Distribution

Token allocation ensures fairness, ecosystem growth, and validation of drug development milestones.

OUR ROADMAP

Molecules.fun Development Timeline

2025
Platform Launch

Q1 2025

Pilot molecules + ecosystem setup

2026
Oracle Integrations

Q2 2026

Smart data feeds & global partnerships

2027
Scaling Buybacks

Q1 2027

Token buyback & burn programs

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CLX-155 — Solid Tumors

Targeted therapy with advantages over Xeloda: extended duration, consistent exposure, safe in liver impairment, potential expanded indications. Status: IND Ready.

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MHG-155A — Glioma

Dual action: HDAC inhibition (valproic acid) + 5-FU DNA/RNA damage. Crosses blood-brain barrier. Extended duration, less variable exposure, safe in liver impairment. Status: PIND Ready.

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OUR TEAM MEMBER

Meet Our
Team