Structure of Talabostat mesylate
CAS No.: 150080-09-4
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Talabostat mesylate (Val-boroPro mesylate; PT100 mesylate) is an orally active, nonselective dipeptidyl peptidase IV (DPP-IV) inhibitor (IC50 < 4 nM; Ki = 0.18 nM) and the first clinical inhibitor of fibroblast activation protein (FAP) (IC50 = 560 nM). It also inhibits DPP8/9 (IC50 = 4/11 nM; Ki = 1.5/0.76 nM), quiescent cell proline dipeptidase (QPP) (IC50 = 310 nM), DPP2, and other DASH family enzymes, exhibiting antineoplastic and hematopoiesis-stimulating activities.
Synonyms: PT100 mesylate; Val-boroPro mesylate; Talabostat (mesylate)
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Batch number can be found on the product's label following the word 'Batch'.
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Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
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CAS No. : | 150080-09-4 |
Formula : | C10H23BN2O6S |
M.W : | 310.17 |
SMILES Code : | CS(=O)(O)=O.CC(C)[C@H](N)C(N1[C@H](B(O)O)CCC1)=O |
Synonyms : |
PT100 mesylate; Val-boroPro mesylate; Talabostat (mesylate)
|
MDL No. : | MFCD13194906 |
InChI Key : | OXYYOEIGQRXGPI-WSZWBAFRSA-N |
Pubchem ID : | 11522448 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P280-P301+P312-P302+P352-P305+P351+P338 |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
4T1 cells | 1.39 µg/mL | To evaluate the cytotoxicity of TRPP in 4T1 cells, the results showed that TRPP exhibited potent cytotoxicity with an IC50 of 1.39 µg/mL. | PMC10091884 | |
CD4+ T cells | 40 ng HIVp24 per million cells | 6 days | To detect the effect of CARD8 deletion on HIV infection, the results showed that CARD8 deletion increased the susceptibility of CD4+ T cells to HIV infection. | PMC10919936 |
Human aortic endothelial cells (HAECs) | 5 µM | 16-18 hours | To validate whether HAECs can undergo inflaμMasome-driven pyroptosis in response to VbP. Results showed that VbP induced cell membrane rupture, GSDMD cleavage, and CASP1 activation, indicating that HAECs can undergo pyroptosis. | PMC9499823 |
A549 cells | 5 µM | 16 hours | To test the response of CARD8 to VbP in A549 cells. Results showed that IL-18 secretion induced by VbP was significantly reduced in CARD8 knockout cells, indicating that CARD8 plays an important role in VbP-induced inflaμMasome activation. | PMC9499823 |
Senescent fibroblasts (SFs) | 200 μg | 48 hours | To evaluate the effect of nanoparticles on SFs, the results showed that PARP1@PLS-PT100 nanoparticles significantly reduced the number of SFs and decreased the expression of SASPs and inflaμMatory factors. | PMC8728814 |
Bone marrow-derived macrophages (BMDMs) | 0.3, 3, 30 μM | 24 hours | To evaluate the effect of Talabostat on NLRP1 inflaμMasome activation, results showed that Nlrp3−/− BMDMs exhibited a significant increase in IL-1β secretion at low doses of Talabostat stimulation, and the LDH levels indicative of cell membrane rupture were also significantly elevated. | PMC6841710 |
HEK ASC-GFP reporter cells | 0.3, 3, 30 μM | 16 hours | To evaluate the sensitivity of different NLRP1 proteins to Talabostat-induced inflaμMasome formation, results showed that HEK reporters expressing NLRP1A exhibited a significant reduction in ASC speck formation in response to Talabostat, while those expressing NLRP1BC57B6 or NLRP1B129S showed no significant difference. | PMC11618613 |
THP-1 macrophages | 2 μM | 24 hours | To study the effects of Val-boroPro on IL-1β expression and secretion, results showed that Val-boroPro significantly increased IL-1β secretion. | PMC5477230 |
primary mouse bone marrow derived macrophages (mBMDMs) | 2 μM | 24 hours | To study the effects of Val-boroPro on cytotoxicity, results showed that Val-boroPro induced LDH release. | PMC5477230 |
primary human peripheral blood mononuclear cells (hPBMCs) | 2 μM | 24 hours | To study the effects of Val-boroPro on cytotoxicity, results showed that Val-boroPro induced LDH release. | PMC5477230 |
RAW 264.7 macrophages | 2 μM | 24 hours | To study the effect of Talabostat on macrophage pyroptosis, results showed that Nlrp1b-deficient macrophages were resistant to Talabostat-induced pyroptosis | PMC5856610 |
HEK 293T cells | 5 μM | 24 hours | To study the effect of Talabostat on HEK 293T cell pyroptosis, results showed that HEK 293T cells expressing Nlrp1b and procaspase-1 were sensitive to Talabostat | PMC5856610 |
myeloma cells | 0.1–100 μmol/l | 5–7 days | PT-100 had no direct effect on myeloma cells cultured alone but significantly inhibited survival of myeloma cells cocultured with osteoclasts. | PMC2748971 |
osteoclast precursors | 0.1–1 μmol/l | 10 days | PT-100 significantly inhibited osteoclast differentiation, reducing the number of multinucleated TRAP-positive osteoclasts. | PMC2748971 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
BALB/c mice | 4T1 tumor model | Intravenous injection | 50 mg/kg/d | Once daily for 10 days | To evaluate the antitumor activity of DPPA-TRPP/Tab in the 4T1 tumor model, the results showed that DPPA-TRPP/Tab significantly suppressed tumor growth with a complete tumor regression (CR) ratio of 60%. | PMC10091884 |
Humanized mice | NSG-SGM3 mice | Retro-orbital injection | DPPA: 0.5 mg/kg, DOX: 0.5 mg/kg, Tab: 1.0 mg/kg | Single dose | To evaluate the role of the CARD8 inflammasome in CD4+ T cell loss during HIV infection, the results showed that CARD8 deletion delayed the loss of CD4+ T cells. | PMC10919936 |
BALB/c mice | 4T1 breast cancer model | Oral | 10 ng p24/mouse | Single injection | Inhibit collagen deposition and enhance the efficacy of anti-PD-1 immunotherapy | PMC11110954 |
Mice | Fap/C0//C0 mice | Oral | 22 weeks | Talabostat markedly improved glucose homeostasis in both Fap+/+ and Fap/C0//C0 mice, independent of FGF21 or FAP. | PMC6323180 | |
mice | Casp1−/− knockout mice | oral | High-fat diet (60 Kcal%) | 7 days before and 7 days after | To study the effects of Val-boroPro on the immune system, results showed that Casp1?/? mice did not show elevation of G-CSF and CXCL1/KC after Val-boroPro treatment. | PMC5477230 |
Mice | Diet-induced obese mice | Oral gavage | 5 mg/kg | Single dose | To evaluate the impact of Talabostat on metabolic regulation, results showed that Talabostat significantly reduced body weight, food intake, adiposity, increased energy expenditure, improved glucose tolerance and insulin sensitivity, and lowered cholesterol levels. | PMC5034526 |
mice | C57BL/6J and 129S6 mice | oral | 3 mg/kg or 10 mg/kg | five times per week for 6 weeks | To study the effect of Talabostat on serum levels of G-CSF and CXCL1/KC in mice, results showed that Talabostat significantly increased the levels of these cytokines | PMC5856610 |
SCID-hu mice | myeloma model | oral | 10 mg/kg/day | for 3 consecutive days | PT-100 significantly reduced myeloma tumour burden and bone disease, inhibiting osteoclast activity and bone resorption. | PMC2748971 |
Clinical Trial:
NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations |
NCT00489710 | Kidney Cancer | Phase 2 | Withdrawn(Terminated for safet... More >>y reasons) Less << | - | - |
NCT02083120 | Pulmonary Disease, Chronic Obs... More >>tructive Less << | Not Applicable | Active, not recruiting | November 2018 | Germany ... More >> Helios Klinik Ambrock Hagen, NRW, Germany, 58091 Less << |
NCT00083239 | Melanoma Skin... More >> Cancer Less << | Phase 2 | Completed | - | United States, Georgia ... More >> Emory University/Winship Cancer Institute Atlanta, Georgia, United States, 30322-1013 United States, Illinois University of Chicago Chicago, Illinois, United States, 60637 United States, Michigan University of Michigan Ann Arbor, Michigan, United States, 48109-0473 United States, New Hampshire Dartmouth-Hitchcock Medical Center Lebanon, New Hampshire, United States, 03756-0001 United States, Pennsylvania University of Pittsburgh Pittsburgh, Pennsylvania, United States, 15213-2582 United States, Texas Mary Crowley Medical Research Center Dallas, Texas, United States, 75246 Less << |
NCT00080080 | Lung Cancer | Phase 2 | Completed | - | United States, Florida ... More >> Cancer Center of Florida Ocoee, Florida, United States, 34761 United States, Illinois University of Chicago Chicago, Illinois, United States, 60637 United States, Michigan Van Elslander Cancer Center Grosse Pointe Woods, Michigan, United States, 48236 United States, New York New York Oncology/Hematology--Albany Regional Cancer Center Albany, New York, United States, 12208 Mt. Sinai School of Medicine New York, New York, United States, 10029 USB Cancer Center-- Nyack Hospital Nyack, New York, United States, 10960 United States, Ohio Dayton Oncology & Hematology Kettering, Ohio, United States, 45409 United States, Texas Mary Crowley Medical Research Center Dallas, Texas, United States, 75246 Tyler Cancer Center Tyler, Texas, United States, 75702 United States, Washington Cancer Care Northwest Spokane, Washington, United States, 99218 Less << |
NCT00083252 | Melanoma Skin... More >> Cancer Less << | Phase 2 | Completed | - | United States, Arkansas ... More >> University of Arkansas Medical Sciences Little Rock, Arkansas, United States, 72205 United States, California Cancer Institute Medical Group, Inc. Santa Monica, California, United States, 90404 United States, Colorado University of Colorado Health Sciences Center Aurora, Colorado, United States, 80045 United States, Florida Cancer Center of Florida Ocoee, Florida, United States, 34761 United States, Indiana Indiana Hematology Oncology Consultants Indianapolis, Indiana, United States, 46202 United States, New Mexico New Mexico Cancer Center Alliance Albuquerque, New Mexico, United States, 87106 United States, New York NYU School of Medicine New York, New York, United States, 10016 Fifth Avenue Medical Healthcare New York, New York, United States, 10128 United States, North Carolina Carolinas Medical Center Charlotte, North Carolina, United States, 28203 United States, South Carolina Cancer Center of the Carolinas Greenville, South Carolina, United States, 29615 United States, Texas Mary Crowley Medical Research Center Dallas, Texas, United States, 75246 Tyler Cancer Center Tyler, Texas, United States, 75702 United States, Washington Cancer Care Northwest Research Spokane, Washington, United States, 99218 Less << |
NCT00086203 | Chronic Lymphocytic Leukemia | Phase 2 | Completed | - | United States, Arkansas ... More >> University of Arkansas for Medical Science Little Rock, Arkansas, United States, 72205 United States, Florida Ocala Oncology Center Ocala, Florida, United States, 34474 Gulfcoast Oncology Associates St. Petersburg, Florida, United States, 33705 United States, Indiana Indiana Oncology/Hematology Consultants Indianapolis, Indiana, United States, 46202 United States, Massachusetts Dana Farber Cancer Institute Boston, Massachusetts, United States, 02115 United States, Montana Hematology/Oncology Centers of the Northern Rockies Billings, Montana, United States, 59101 United States, Nevada Nevada Cancer Institute Las Vegas, Nevada, United States, 89135 United States, New York Queens Medical Associates, PC Fresh Meadows, New York, United States, 11365 Long Island Jewish Medical Center New Hyde Park, New York, United States, 11040 NYU Medical Center New York, New York, United States, 10016 James P. Wilmot Cancer Center/University of Rochester Rochester, New York, United States, 14642 United States, North Carolina Raleigh Hematology/Oncology Clinic Cary, North Carolina, United States, 27511 Wake Forest University Health Sciences Winston-Salem, North Carolina, United States, 27157 United States, Oklahoma Cancer Care Associates/Oklahoma City Oklahoma City, Oklahoma, United States, 73112 Cancer Care Associates--Tulsa Tulsa, Oklahoma, United States, 74136 United States, South Carolina Cancer Centers of the Carolinas Seneca, South Carolina, United States, 29672 United States, Texas Texas Cancer Center/Abilene Abilene, Texas, United States, 79606-5208 MD Anderson Cancer Center Houston, Texas, United States, 77030 United States, Virginia Virginia Oncology Associates-Lake Wright Cancer Center Norfolk, Virginia, United States, 23502 Less << |
NCT00116389 | Pancreatic Cancer ... More >> Neoplasm Metastasis Adenocarcinoma Less << | Phase 2 | Terminated(FDA Hold May 2007) | - | - |
NCT00243204 | Carcinoma, Non-Small Cell Lung | Phase 3 | Terminated(FDA Hold May 2007) | - | - |
NCT00303940 | Brain and Central Nervous Syst... More >>em Tumors Childhood Germ Cell Tumor Kidney Cancer Liver Cancer Neuroblastoma Ovarian Cancer Sarcoma Unspecified Childhood Solid Tumor, Protocol Specific Less << | Phase 1 | Completed | - | United States, Maryland ... More >> Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office Bethesda, Maryland, United States, 20892-1182 Less << |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
3.22mL 0.64mL 0.32mL |
16.12mL 3.22mL 1.61mL |
32.24mL 6.45mL 3.22mL |
|
Dissolving Methods |
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:
in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day; The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
|
Tags: Talabostat | Val-boroPro | PT100 | PT 100 | PT-100 | Dipeptidyl Peptidase | DPP | Val-boroPro | DPP-IV inhibitor | fibroblast activation protein | antineoplastic | hematopoiesis-stimulating | 150080-09-4
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P272 | Contaminated work clothing should not be allowed out of the workplace. |
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Response | |
Code | Phrase |
P301 | IF SWALLOWED: |
P304 | IF INHALED: |
P305 | IF IN EYES: |
P306 | IF ON CLOTHING: |
P307 | IF exposed: |
P308 | IF exposed or concerned: |
P309 | IF exposed or if you feel unwell: |
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P340 | Remove victim to fresh air and keep at rest in a position comfortable for breathing. |
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P342 | If experiencing respiratory symptoms: |
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P371 | In case of major fire and large quantities: |
P372 | Explosion risk in case of fire. |
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P374 | Fight fire with normal precautions from a reasonable distance. |
P376 | Stop leak if safe to do so. Oxidising gases (section 2.4) 1 |
P377 | Leaking gas fire: Do not extinguish, unless leak can be stopped safely. |
P378 | |
P380 | Evacuate area. |
P381 | Eliminate all ignition sources if safe to do so. |
P390 | Absorb spillage to prevent material damage. |
P391 | Collect spillage. Hazardous to the aquatic environment |
P301 + P310 | IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. |
P301 + P312 | IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell. |
P301 + P330 + P331 | IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. |
P302 + P334 | IF ON SKIN: Immerse in cool water/wrap in wet bandages. |
P302 + P350 | IF ON SKIN: Gently wash with plenty of soap and water. |
P303 + P361 + P353 | IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower. |
P304 + P312 | IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell. |
P304 + P340 | IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. |
P304 + P341 | IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. |
P305 + P351 + P338 | IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. |
P306 + P360 | IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes. |
P307 + P311 | IF exposed: call a POISON CENTER or doctor/physician. |
P308 + P313 | IF exposed or concerned: Get medical advice/attention. |
P309 + P311 | IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician. |
P332 + P313 | IF SKIN irritation occurs: Get medical advice/attention. |
P333 + P313 | IF SKIN irritation or rash occurs: Get medical advice/attention. |
P335 + P334 | Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages. |
P337 + P313 | IF eye irritation persists: Get medical advice/attention. |
P342 + P311 | IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician. |
P370 + P376 | In case of fire: Stop leak if safe to Do so. |
P370 + P378 | In case of fire: |
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P370 + P380 + P375 | In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion. |
P371 + P380 + P375 | In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion. |
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Code | Phrase |
P401 | |
P402 | Store in a dry place. |
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P420 | Store away from other materials. |
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P403 + P233 | Store in a well-ventilated place. Keep container tightly closed. |
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P410 + P403 | Protect from sunlight. Store in a well-ventilated place. |
P410 + P412 | Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF. |
P411 + P235 | Keep cool. |
Disposal | |
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P502 | Refer to manufacturer/supplier for information on recovery/recycling |
Physical hazards | |
Code | Phrase |
H200 | Unstable explosive |
H201 | Explosive; mass explosion hazard |
H202 | Explosive; severe projection hazard |
H203 | Explosive; fire, blast or projection hazard |
H204 | Fire or projection hazard |
H205 | May mass explode in fire |
H220 | Extremely flammable gas |
H221 | Flammable gas |
H222 | Extremely flammable aerosol |
H223 | Flammable aerosol |
H224 | Extremely flammable liquid and vapour |
H225 | Highly flammable liquid and vapour |
H226 | Flammable liquid and vapour |
H227 | Combustible liquid |
H228 | Flammable solid |
H229 | Pressurized container: may burst if heated |
H230 | May react explosively even in the absence of air |
H231 | May react explosively even in the absence of air at elevated pressure and/or temperature |
H240 | Heating may cause an explosion |
H241 | Heating may cause a fire or explosion |
H242 | Heating may cause a fire |
H250 | Catches fire spontaneously if exposed to air |
H251 | Self-heating; may catch fire |
H252 | Self-heating in large quantities; may catch fire |
H260 | In contact with water releases flammable gases which may ignite spontaneously |
H261 | In contact with water releases flammable gas |
H270 | May cause or intensify fire; oxidizer |
H271 | May cause fire or explosion; strong oxidizer |
H272 | May intensify fire; oxidizer |
H280 | Contains gas under pressure; may explode if heated |
H281 | Contains refrigerated gas; may cause cryogenic burns or injury |
H290 | May be corrosive to metals |
Health hazards | |
Code | Phrase |
H300 | Fatal if swallowed |
H301 | Toxic if swallowed |
H302 | Harmful if swallowed |
H303 | May be harmful if swallowed |
H304 | May be fatal if swallowed and enters airways |
H305 | May be harmful if swallowed and enters airways |
H310 | Fatal in contact with skin |
H311 | Toxic in contact with skin |
H312 | Harmful in contact with skin |
H313 | May be harmful in contact with skin |
H314 | Causes severe skin burns and eye damage |
H315 | Causes skin irritation |
H316 | Causes mild skin irritation |
H317 | May cause an allergic skin reaction |
H318 | Causes serious eye damage |
H319 | Causes serious eye irritation |
H320 | Causes eye irritation |
H330 | Fatal if inhaled |
H331 | Toxic if inhaled |
H332 | Harmful if inhaled |
H333 | May be harmful if inhaled |
H334 | May cause allergy or asthma symptoms or breathing difficulties if inhaled |
H335 | May cause respiratory irritation |
H336 | May cause drowsiness or dizziness |
H340 | May cause genetic defects |
H341 | Suspected of causing genetic defects |
H350 | May cause cancer |
H351 | Suspected of causing cancer |
H360 | May damage fertility or the unborn child |
H361 | Suspected of damaging fertility or the unborn child |
H361d | Suspected of damaging the unborn child |
H362 | May cause harm to breast-fed children |
H370 | Causes damage to organs |
H371 | May cause damage to organs |
H372 | Causes damage to organs through prolonged or repeated exposure |
H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
Code | Phrase |
H400 | Very toxic to aquatic life |
H401 | Toxic to aquatic life |
H402 | Harmful to aquatic life |
H410 | Very toxic to aquatic life with long-lasting effects |
H411 | Toxic to aquatic life with long-lasting effects |
H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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