BETABiohacksAI is a research tool for informational purposes only. All outputs are computational hypothesis candidates — not confirmed mechanisms, not medical advice, and not a substitute for professional medical judgment. Independent experimental validation is always required.
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BiohacksAI/Targets/CCAR1/Compounds

Compounds That Target CCAR1

CCAR1 · 16 compounds in BiohacksAI corpus

CCAR1 (CCAR1) is a biological target with 16 documented compound interactions in the BiohacksAI corpus. The compounds listed below have been identified through computational analysis of BindingDB binding assay data and PubMed literature. Each interaction is ranked by confidence score reflecting the breadth and strength of experimental evidence. This resource supports research into CCAR1 modulation for therapeutic and biohacking applications.

View CCAR1 target page →
Most Studied Compounds for CCAR1
1
Allium Sativum
500+
studies
2
Foeniculum Vulgare
499+
studies
3
Zingiber Officinale
498+
studies
All 16 Compounds — Ranked by Evidence
1
Eriobotrya Japonica
1.00
confidence
2
Glycine Max
1.00
confidence
3
Zingiber Officinale
498+
studies
1.00
confidence
4
Aconitum Carmichaelii
0.50
confidence
5
Agastache Rugosa
0.50
confidence
6
Allium Sativum
500+
studies
0.50
confidence
7
Carthamus Tinctorius
0.50
confidence
8
Chaenomeles Speciosa
0.50
confidence
9
Coix Lacryma
0.50
confidence
10
Foeniculum Vulgare
499+
studies
0.50
confidence
11
Fritillaria Cirrhosa
0.50
confidence
12
Litchi Chinensis
0.50
confidence
13
Morus Alba
0.50
confidence
14
Nelumbo Nucifera
0.50
confidence
15
Peucedanum Praeruptorum
0.50
confidence
16
Uncaria Rhynchophylla
0.50
confidence

The compounds above were identified through computational analysis of BindingDB binding assay data and PubMed literature for CCAR1 (CCAR1). Confidence scores reflect the strength and breadth of experimental evidence.

Explore related resources: CCAR1 target overview · All biological targets · Biological pathways

Data from BindingDB and PubMed. For research purposes only. Not medical advice.