Author: kodiac

  • P21 (Cerebrolysin-derived peptide)

    Plain-language summaryIntrigue 65 / 100

    P21 is a synthetic peptide derived from ciliary neurotrophic factor (CNTF) developed for neuroprotection and neurogenesis. Used in research for memory and Alzheimer disease investigations. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    CNTF-derived neurogenic peptide

    A short peptide derived from a cerebrolysin fraction with documented hippocampal neurogenesis activity in animal models.

    Abstract

    P21 is a peptide of the sequence Ala-Asp-Asn-Phe-Val-Phe-Lys derived from the active fraction of cerebrolysin (or related neurotrophic preparations) and identified by Khalid Iqbal’s group at the New York State Institute for Basic Research. The compound stimulates neurogenesis in the dentate gyrus through a CNTF-receptor-related mechanism, producing dose-dependent improvements in spatial learning and memory in rodent models of cognitive aging and Alzheimer disease pathology. The compound has not been advanced to human clinical trials. Pharmacokinetics are poorly characterized in humans. The compound is sold as a research peptide; investigational doses parallel cerebrolysin range scaled to peptide content.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.

  • Davunetide (NAP)

    Plain-language summaryIntrigue 65 / 100

    Davunetide (NAP) is an 8-amino-acid peptide derived from activity-dependent neuroprotective protein (ADNP). It supports microtubule integrity in neurons. Phase 2/3 trials in progressive supranuclear palsy were inconclusive. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    ADNP-derived octapeptide

    An eight-amino-acid fragment of activity-dependent neuroprotective protein (ADNP) studied in tauopathies and PSP.

    Abstract

    Davunetide (NAP, AL-108; Asn-Ala-Pro-Val-Ser-Ile-Pro-Gln; CAS 173308-60-2; molecular weight 824.94) is an octapeptide derived from activity-dependent neuroprotective protein (ADNP). The peptide preserves microtubule integrity and reduces tau pathology in animal models of tauopathy. Davunetide was developed by Allon Therapeutics and advanced through Phase 2/3 trials in progressive supranuclear palsy (PSP); the pivotal trial in 2012 was negative for the primary cognitive endpoint, ending the development program. The compound is administered intranasally (the primary route of delivery to CNS for the formulation used in trials). Research-grade doses are 5 to 30 mg intranasally per day.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.

  • ARA-290 (Cibinetide)

    Plain-language summaryIntrigue 78 / 100

    ARA-290 (cibinetide) is an 11-amino-acid peptide derived from the helix B portion of erythropoietin. It activates a tissue-protective receptor without raising hematocrit. Investigated for neuropathic pain. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    EPO-derived helix B peptide

    An 11-amino-acid fragment of erythropoietin’s helix B with tissue-protective activity but without erythropoietic activity.

    Abstract

    ARA-290 (Cibinetide; Gln-Glu-Gln-Leu-Glu-Arg-Ala-Leu-Asn-Ser-Ser; CAS 1208243-50-8) is an 11-residue peptide derived from the alpha-helix B region of erythropoietin (EPO). The peptide retains the tissue-protective and anti-inflammatory activity of EPO (mediated through the heteromeric EPO/CD131 innate repair receptor) without the erythropoietic activity (mediated through the EPO receptor homodimer). The compound was developed by Araim Pharmaceuticals for diabetic neuropathy, sarcoidosis-associated small fiber neuropathy, and other neuropathic pain indications. Phase 2 trials in sarcoidosis-associated SFN showed reductions in neuropathic pain and improvements in autonomic measures. Doses are 4 mg subcutaneously per day in clinical trials.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.

  • Thymulin

    Plain-language summaryIntrigue 50 / 100

    Thymulin is a 9-amino-acid zinc-dependent thymic hormone that regulates T-cell development. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    Zinc-dependent thymic nonapeptide

    A zinc-dependent endogenous thymic nonapeptide secreted by thymic epithelial cells with T-cell maturation activity.

    Abstract

    Thymulin (Pyr-Ala-Lys-Ser-Gln-Gly-Gly-Ser-Asn; molecular weight 857) is a nonapeptide originally isolated by Bach and Goldstein groups in the 1970s. The peptide is endogenously secreted by thymic epithelial cells and requires bound zinc for biological activity. Pharmacology includes promotion of T-cell differentiation, modulation of cytokine balance, and effects on autoimmune and inflammatory processes. The compound has been studied in chronic infections, autoimmune diseases, and cancer immunotherapy adjunct applications, with limited Phase 2 evidence. Available as research peptide. Doses are typically 100 to 1000 micrograms per administration.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.

  • Thymogen

    Plain-language summaryIntrigue 45 / 100

    Thymogen is a synthetic dipeptide (Glu-Trp) immunomodulator developed in Russia, derived from research on thymic hormones. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    Synthetic dipeptide immunomodulator

    A synthetic dipeptide (Glu-Trp) developed in Russia as an immunomodulator for infectious and post-surgical immune support.

    Abstract

    Thymogen is the dipeptide L-glutamyl-L-tryptophan, developed in Russia at the Institute of Bioregulation and Gerontology. The compound was identified through fractionation of thymalin (bovine thymus extract) as one of the active components. Thymogen is approved in Russia and several former Soviet states for infectious diseases, post-surgical immune support, and hematopoietic recovery after chemotherapy. Mechanism includes modest T-cell maturation effects and cytokine modulation. Administered intranasally or intramuscularly. Doses are 100 micrograms per day in 3 to 10 day courses.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.

  • Thymopentin

    Plain-language summaryIntrigue 50 / 100

    Thymopentin is a 5-amino-acid synthetic peptide representing the active region of thymopoietin. Used historically for psoriasis and immune modulation. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    Synthetic pentapeptide of thymopoietin

    A synthetic pentapeptide fragment (residues 32-36) of thymopoietin marketed in Europe and Asia for immunomodulation in chronic infections and autoimmune disease.

    Abstract

    Thymopentin (Timunox, TP-5; Arg-Lys-Asp-Val-Tyr; CAS 69558-55-0; molecular weight 679.78) is a synthetic pentapeptide corresponding to residues 32-36 of thymopoietin, a thymic hormone. The fragment retains the immunomodulatory activity of full-length thymopoietin. The compound is approved in Italy and several Asian countries for primary immunodeficiency, hepatitis B, atopic dermatitis adjunct, and autoimmune disease support. Mechanism includes T-cell maturation, NK cell modulation, and cytokine balance effects. Administered subcutaneously. Doses are 50 mg three times weekly in clinical use.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.

  • Gepirone

    Plain-language summaryIntrigue 64 / 100

    Gepirone (Exxua) finally reached FDA approval in 2023, more than thirty years after its initial development at Bristol-Myers Squibb began in the 1980s. The 5-HT1A partial agonist had been rejected by the FDA multiple times before Fabre-Kramer eventually pushed an extended-release formulation across the finish line for major depressive disorder. The selling point versus standard SSRIs is essentially zero sexual dysfunction, which is the side effect that drives many patients off serotonergic antidepressants. Mechanistically it is in the same azapirone family as buspirone but with substantially more 5-HT1A intrinsic activity, which appears to translate into antidepressant rather than just anxiolytic effects. Real-world prescribing data are still accumulating. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    5-HT1A partial agonist

    An azapirone 5-HT1A partial agonist developed for major depressive disorder; FDA-approved in 2023 after a 30-year development cycle.

    Abstract

    Gepirone (4,4-dimethyl-1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl}-2,6-piperidinedione; CAS 83928-76-1; molecular formula C19H29N5O2; molecular weight 359.47) is an azapirone 5-HT1A partial agonist developed by Bristol-Myers Squibb and Fabre-Kramer over a 30-plus-year development cycle, ultimately approved by the FDA in 2023 under the trade name Exxua for major depressive disorder. The compound is structurally and mechanistically similar to buspirone: 5-HT1A affinity approximately 19 nM with intrinsic activity approximately 60 percent; minimal D2 affinity; active metabolite 1-PP. Distinct from buspirone in development trajectory (positioned for depression rather than anxiety) and in being formulated as extended-release for once-daily dosing. The approved indication is MDD; the principal selling point versus SSRIs is absence of sexual dysfunction (a major SSRI tolerability complaint). Plasma half-life is 18 hours (ER formulation); metabolism is via CYP3A4. Used as a reference 5-HT1A partial agonist with depression-focused clinical development.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.

  • Tandospirone

    Plain-language summaryIntrigue 47 / 100

    Tandospirone (Sediel, Senparen) is a Japanese-developed second-generation azapirone from Sumitomo, approved in Japan in 1996 and China in 2004. It has not been pursued in Western markets. Mechanistically it is closely related to buspirone, partially activating the serotonin 5-HT1A receptor, but with somewhat higher intrinsic activity at the receptor (around 60 percent versus buspirone’s 35 percent). Used for generalized anxiety and adjustment disorders, with some research interest in cognitive effects through 5-HT1A in the prefrontal cortex. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    5-HT1A partial agonist anxiolytic (Asian markets)

    A second-generation azapirone 5-HT1A partial agonist marketed in Japan and China; not approved in Western markets.

    Abstract

    Tandospirone ((1R,2R,6S,7S)-4-(4-{[4-(pyrimidin-2-yl)piperazin-1-yl]butyl})-4-azatricyclo[5.2.1.02,6]decane-3,5-dione; CAS 87760-53-0; molecular formula C21H29N5O2; molecular weight 383.49) is a second-generation azapirone 5-HT1A partial agonist developed at Sumitomo and approved in Japan in 1996 (Sediel) and China in 2004 (Senparen). Receptor profile is closely related to buspirone: 5-HT1A affinity approximately 27 nM (intrinsic activity approximately 60 percent, higher than buspirone); minimal D2 affinity. Compared to buspirone, the higher 5-HT1A intrinsic activity is hypothesized to produce somewhat greater anxiolytic and antidepressant effect. Plasma half-life is approximately 1 hour; metabolism is via CYP3A4 with active metabolite 1-PP common to the azapirone class. Approved indications include generalized anxiety disorder and adjustment disorder with anxiety; off-label use in depression. Not approved in the US or EU. Used as a reference azapirone with higher 5-HT1A intrinsic activity than buspirone in mechanism studies.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.

  • Buspirone

    Plain-language summaryIntrigue 60 / 100

    Buspirone (BuSpar) is the first non-benzodiazepine anxiolytic, approved by the FDA in 1986. Mechanistically it is unrelated to any sedative class: it is a partial agonist at the serotonin 5-HT1A receptor, with no GABA-A activity. That means it does not produce sedation, dependence, or withdrawal, and it has no recreational potential. The trade-off is that it works slowly (effects build over 2 to 4 weeks) and does not produce the fast acute relief patients expect from a benzodiazepine, which has limited its uptake despite its safety advantages. It is FDA-approved for generalized anxiety disorder and is widely used as add-on for SSRI-treated depression where some additional anxiolysis is needed. The active metabolite 1-PP is an alpha-2 antagonist contributing to the noradrenergic tone. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    5-HT1A partial agonist anxiolytic

    An azapirone 5-HT1A partial agonist; a non-benzodiazepine anxiolytic without dependence or sedation.

    Abstract

    Buspirone (8-[4-(4-pyrimidin-2-yl-1-piperazinyl)butyl]-8-azaspiro[4.5]decane-7,9-dione; CAS 36505-84-7; molecular formula C21H31N5O2; molecular weight 385.50) is an azapirone 5-HT1A partial agonist developed at Bristol-Myers Squibb and approved by the FDA in 1986 under the trade name BuSpar. The compound is the first clinically approved non-benzodiazepine anxiolytic, distinguished by mechanism (5-HT1A partial agonism rather than GABA-A potentiation), tolerance/dependence profile (none), and absence of sedation. 5-HT1A affinity is approximately 21 nM (intrinsic activity approximately 35 percent); secondary D2 antagonism (Ki approximately 100 nM) is of unclear clinical significance. The active metabolite 1-(2-pyrimidinyl)piperazine (1-PP) is an alpha-2 adrenergic antagonist contributing to noradrenergic effects. Onset of anxiolytic effect is delayed (2 to 4 weeks), reflecting the time course of 5-HT1A autoreceptor desensitization. Plasma half-life is 2 to 3 hours; metabolism is extensive via CYP3A4 with significant first-pass effect (oral bioavailability approximately 4 percent). Approved for generalized anxiety disorder. Used as the canonical 5-HT1A partial agonist in mechanism studies.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.

  • Vigabatrin

    Plain-language summaryIntrigue 69 / 100

    Vigabatrin (Sabril) is a so-called suicide inhibitor of GABA transaminase, the enzyme that breaks down the brain’s main inhibitory neurotransmitter. The vinyl group on the molecule converts vigabatrin into a fake substrate that the enzyme attempts to process and is then permanently destroyed by; the only way the brain restores normal GABA breakdown is to manufacture new enzyme from scratch. The result is sustained and powerful elevation of brain GABA levels. It is uniquely effective in infantile spasms (a devastating early-childhood seizure disorder) and refractory complex partial seizures. The catch is severe and irreversible: roughly a third of patients develop permanent visual field constriction from retinal toxicity. That has restricted it to cases where no alternative works. Not stocked by Kodiac. This monograph is provided for research and educational reference.

    Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.

    GABA transaminase inhibitor (irreversible)

    An irreversible suicide inhibitor of GABA transaminase; uniquely effective in infantile spasms and refractory complex partial seizures, limited by retinal toxicity.

    Abstract

    Vigabatrin ((R/S)-4-aminohex-5-enoic acid; CAS 60643-86-9; molecular formula C6H11NO2; molecular weight 129.16) is a vinyl-GABA suicide inhibitor of GABA transaminase developed at Marion Merrell Dow and approved by the FDA in 2009 under the trade name Sabril (later than European registration in 1989). Mechanism: the vinyl group at the alpha-carbon converts vigabatrin into a substrate that the GABA transaminase enzyme begins to process but cannot release; the result is irreversible covalent enzyme inactivation, requiring de novo enzyme synthesis to recover GABA degradation capacity. The consequence is sustained elevation of brain GABA concentrations. Effective in infantile spasms (West syndrome) where conventional anticonvulsants often fail, and as adjunctive therapy in refractory complex partial seizures. The principal limitation is irreversible bilateral concentric visual field constriction in approximately 30 to 50 percent of long-term users, attributed to retinal photoreceptor damage; the FDA REMS program requires baseline and periodic visual field assessment. Plasma half-life is 5 to 13 hours, but the irreversible enzyme inhibition produces effective activity beyond the plasma window. Used as the canonical GABA transaminase suicide inhibitor.

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    FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.