The go-to herb for PMS and menstrual irregularities. Works by gently rebalancing prolactin and progesterone. Binds to dopamine D2 receptors in the pituitary, lowering prolactin. This allows progesterone to normalize, correcting the hormonal imbalance behind most PMS symptoms.
Reviewed March 2026
These words describe the research, not the molecule's worth. Research strength is how much work stands behind one claim, and it is never a product score.
A pairing appears on this page only when a trial gave both ingredients together and measured the result. Chaste Tree has none that clears that bar.
Stitching two separate single-ingredient studies into a pairing is the one thing this engine will not do. When a study of the combination itself holds up at source, it lands here with its citation.
No invented synergy. Where actives were studied on their own rather than together, the record shows each on its own evidence, never a combined effect no trial measured.
Research strength. Research strength says how much work stands behind the combination. It is never a product score.
Independent record. Every finding is cited to a named trial, dated, and never written by the brand.
20 pairings are live across the library today. Checked 20 July 2026.
No study gave these as a pair, so they are not in the card above. But the reason they belong together is settled biochemistry, not a guess, so it is worth knowing.
B6 as pyridoxal-5-phosphate is the cofactor for the decarboxylase step that makes dopamine, and dopamine tone at the pituitary is what sets prolactin output. Vitex acts on that same dopaminergic receptor side.
P5P is the ready-to-use coenzyme form for aromatic amino acid decarboxylase, the enzyme that produces dopamine. Vitex works on dopamine receptor signalling, so cofactor supply and receptor action line up.
Magnesium supports smooth muscle relaxation and works with B6 in neurotransmitter enzymes, a standing pairing with vitex in monthly cycle formulas. The mechanisms are separate and non-competing.
Black cohosh acts on serotonergic and central pathways rather than the dopamine and prolactin axis vitex works on. Formulas for midlife hormonal change combine the two for that reason.
Dong quai coumarins support circulation and smooth muscle tone while vitex works at the pituitary. They occupy different roles in classic cyclical blends.
Evening primrose GLA feeds the series-1 prostaglandin pathway that governs breast and tissue comfort, a route vitex does not act on. The two are long-standing companions in cyclical formulas.
Saffron crocins act on serotonin reuptake and mood pathways, separate from vitex's dopaminergic effect on prolactin. Cyclical mood formulas pair them for that split.
Mucuna supplies L-dopa, a direct dopamine precursor, while vitex acts as a dopamine receptor agonist at the pituitary. Stacking both pushes the same axis from two directions and the combined effect on prolactin can be larger than intended.
Calcium is a standard component of cycle-support formulas and acts on neuromuscular and smooth-muscle signalling, a different lever from a dopaminergic plant extract. The two are combined for coverage rather than for an interaction. No trial has measured the pair.
Vitamin D drives the calcium-binding transport proteins that make intestinal calcium absorption efficient, so it belongs next to any calcium in the same formula. Its relationship is with the mineral, not with the plant extract. Established physiology with no combination data for chaste tree.
Myo-inositol and its phosphorylated derivatives are second messengers downstream of several peptide hormone receptors, including gonadotropin signalling in the ovary. Chaste tree acts higher up, at pituitary prolactin release through dopamine receptors. The two touch different points of the same axis and have not been trialled together.
Zinc is a cofactor in steroid hormone receptor function, since the classic nuclear receptor DNA-binding domain is a zinc finger. It also supports normal reproductive tissue function generally. This is background physiology rather than a measured effect with the extract.
GLA is elongated to dihomo-gamma-linolenic acid, the precursor of series-1 prostaglandins, which is why it appears in cycle-comfort formulas. It works on lipid mediators; chaste tree works on pituitary prolactin release. The stored partner evening primrose oil is the usual GLA source, so a formula should not double the same fatty acid unknowingly.
Ashwagandha withanolides are studied for their effect on the hypothalamic-pituitary-adrenal axis and cortisol output, while chaste tree diterpenes act on dopamine receptors at the pituitary. Both touch pituitary output but at different cell populations and hormones. Combination products exist; combination trials do not.
Rhodiola salidrosides and rosavins are studied for stress-axis and monoamine effects; chaste tree is dopaminergic at the pituitary. Because both touch monoamine signalling, the combination is worth flagging as overlapping rather than purely additive. Nothing has been measured together.
Chamomile apigenin binds GABA-A receptors at benzodiazepine-adjacent sites in laboratory work, giving it a calming character. Chaste tree is not sedating, so in a blend chamomile carries that property alone. Stacking several calming botanicals can add up, which matters before driving.
Lemon balm constituents inhibit GABA transaminase in laboratory assays, which raises GABA availability. It is a common partner in evening cycle-support blends. The additive calming effect with other GABAergic botanicals is the practical consideration, not an interaction with chaste tree itself.
St John's wort hyperforin activates the pregnane X receptor and induces CYP3A4 and P-glycoprotein, which lowers exposure to many co-administered compounds including hormonal contraceptives. That induction is the single most important thing to know about the pairing, whatever the chaste tree does. Anyone on prescription medicine should raise the combination with a clinician before taking it.
5-HTP is decarboxylated to serotonin by aromatic L-amino acid decarboxylase, the same enzyme that converts L-DOPA to dopamine, so the two substrates compete for it. Chaste tree acts at dopamine receptors rather than on synthesis, but stacking monoamine-active ingredients deserves care and is a reason to involve a clinician if any serotonergic medicine is in play.
Tyrosine is hydroxylated to L-DOPA and decarboxylated to dopamine, so it supplies the substrate side of dopaminergic signalling. Chaste tree diterpenes act on the receptor side. Substrate and receptor are complementary points in one pathway, though the pair has not been studied together.
Menstrual blood loss is the main route of iron loss in menstruating adults, which is why iron sits in cycle-support formulas. It has no pharmacological relationship with chaste tree. Iron absorption is improved by vitamin C and reduced by tea polyphenols and calcium taken in the same dose, so timing matters more than the botanical pairing.
Talk to a doctor before taking Chaste Tree if any of these apply to you: Don't use with hormonal contraceptives, Avoid during pregnancy and breastfeeding, Takes 2-3 months for full effect. These are flags to check first, not effects Chaste Tree is known to cause.
Not medical advice. Show the label to your pharmacist.The whole-food sources on file. A supplement closes the gap, it does not replace dinner.
A gram-for-gram figure (how much of each you would eat to match a dose) will appear here once it is sourced and reviewed. This page will not print a number it cannot cite.
These are the studies our verdict leans on, chosen from the 2 we read for Chaste Tree. The full linked list is below.
Read this carefully. These are 10,859 voluntary, unverified reactions reported to the FDA (openFDA). The number mostly reflects how popular Chaste Tree is, not how risky it is. A report is not proof Chaste Tree caused anything. It is a signal of what to watch for, nothing more.
Source: openFDA adverse-event reports. Voluntary reporting, not an incidence rate.
FDA Disclaimer: These statements have not been evaluated by the Food and Drug Administration. This information is for educational purposes only and is not intended to diagnose, treat, cure, or prevent any disease. Consult your healthcare provider before starting any supplement regimen.