data + articles · 4 listed
newest 2026spec sheet11 rows
JBSNF-000088 is a small-molecule inhibitor of nicotinamide N-methyltransferase (NNMT), a cytosolic enzyme that methylates nicotinamide using S-adenosylmethionine [1]. Originally reported as a nicotinamide analogue that reduces 1-methylnicotinamide levels and improves insulin sensitivity and body weight in obese and diabetic mice, it has since become a widely used NNMT-inhibitor tool compound in cancer and metabolic research [1]. Notably, it is not a TAAR1 agonist or monoamine modulator; its target is NNMT.
- Selective, target-validated NNMT inhibition confirmed by knockout controls and co-crystal structures
- Improved insulin sensitivity and glucose tolerance in obese/diabetic mouse models
- Frequently mislabeled as a CNS/monoamine agent, which it is not
Overview
NNMT sits at the intersection of NAD-plus and methylation metabolism, and elevated NNMT activity has been associated with obesity, type 2 diabetes, and tumor progression. JBSNF-000088 was characterized as a slow-turnover substrate analogue that binds NNMT and, upon N-methylation, remains associated with the enzyme; co-crystal structures captured its methylated product bound in the active site [1].
In high-fat-diet-induced obese mice, JBSNF-000088 lowered 1-methylnicotinamide, reduced body weight, improved insulin sensitivity, and normalized glucose tolerance to lean-control levels, effects that were absent in NNMT-knockout mice, confirming on-target specificity [1]. Subsequent studies repurposed the compound as an NNMT probe in oncology, where NNMT inhibition reduced proliferation, migration, and invasion in models of gallbladder carcinoma, endometriosis-associated stromal cells, lung-cancer drug resistance, and ovarian cancer [2][3][4][1].
JBSNF-000088 is a preclinical research chemical with no human data and no CNS or nootropic indication. Its inclusion here corrects a common misattribution: it is an NNMT enzyme inhibitor arising from metabolic-disease drug discovery, not a monoaminergic or trace-amine compound.
- Contrary to some listings, JBSNF-000088 is not a TAAR1 or monoamine compound; it inhibits the enzyme NNMT.
- It was first developed for obesity and type 2 diabetes, where it normalized glucose tolerance in obese mice.
- It works as a 'slow-turnover' substrate that gets methylated and then stays stuck in the enzyme's active site.
Mechanism
JBSNF-000088 is a nicotinamide analogue that inhibits NNMT by acting as a slow-turnover substrate: it occupies the enzyme's nicotinamide-binding site and is itself N-methylated, with the methylated product remaining bound, thereby blocking methylation of endogenous nicotinamide and lowering 1-methylnicotinamide output [1]. By reducing NNMT flux, the compound preserves cellular NAD-plus and methyl-donor pools and modulates downstream signaling; in tumor models NNMT inhibition suppresses pro-proliferative and pro-invasive pathways [2][3][4][1].
receptor fingerprint
Nicotinamide N-methyltransferase (NNMT)Inhibitor (slow-turnover substrate analogue)
NAD-plus / methylation metabolismModulator
Dosingtypical ranges, not medical advice
interested in protocols and clinical dosages? make an account to see them! ^_^
Safetyrisks and cautions, not medical advice
JBSNF-000088 is an investigational, preclinical research compound supplied for laboratory use only (RUO); it is not approved for human use and is not a dietary supplement. It was reported to be effective and specific in rodent studies, but no controlled human safety data exist [1]. Because NNMT participates in core metabolic and methylation pathways, systemic effects of chronic inhibition in humans are unknown. Self-administration is not advised.
History
JBSNF-000088 was described in a 2018 collaboration between Sanofi and Jubilant Biosys as a small-molecule NNMT inhibitor for metabolic disorders, characterized structurally and pharmacologically in animal models of obesity and type 2 diabetes [1]. It was subsequently adopted as a reference NNMT inhibitor across independent cancer and reproductive-biology studies from 2023 onward [2][3][4][1].
Reputation
In metabolic and cancer research, JBSNF-000088 is regarded as a useful, target-validated NNMT inhibitor tool compound. Outside that literature it is frequently and incorrectly described as a CNS or monoamine agent; the peer-reviewed record clearly identifies it as an NNMT inhibitor with metabolic and oncologic activity [1][2]. It has no legitimate standing as a human therapeutic or nootropic.
Subjective profileweighing the evidence above
A well-validated laboratory tool and nothing more. The insulin-sensitivity and weight results are mouse data, there is no human safety information, and the compound is routinely mislabeled as a CNS or monoamine agent, which tells you how carefully whatever listing you are reading was written.
Resources
This entry is here for reference.
Research
- 2018first citedA small molecule inhibitor of Nicotinamide N-methyltransferase for the treatment of metabolic d…
- 2026most recentNicotinamide N-methyltransferase promotes drug resistance in lung cancer, as revealed by nascen…
- 1.A small molecule inhibitor of Nicotinamide N-methyltransferase for the treatment of metabolic disorders.
- 2.Nicotinamide N -methyltransferase promotes M2 macrophage polarization by IL6 and MDSC conversion by GM-CSF in gallbladder carcinoma.
- 3.Overexpressed nicotinamide N‑methyltransferase in endometrial stromal cells induced by macrophages and estradiol contributes to cell proliferation in endometriosis.
- 4.Nicotinamide N-methyltransferase promotes drug resistance in lung cancer, as revealed by nascent proteomic profiling.
4 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
What is the actual target of JBSNF-000088?
It inhibits nicotinamide N-methyltransferase (NNMT), an enzyme in NAD and methylation metabolism. It is not a TAAR1 agonist or a monoamine reuptake modulator, despite some listings suggesting otherwise.
What has JBSNF-000088 been studied for?
Originally for obesity and type 2 diabetes in mice, and more recently as an NNMT-inhibitor tool in cancer research. All data are preclinical; there is no approved human use.
Limitations of the evidence
- No human safety data; effects of chronic NNMT inhibition on human metabolism unknown
Adverse effects
- Frequently mislabeled as a CNS/monoamine agent, which it is not