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Product information|CAS Number: 1794937-18-0|Molecular Weight: 278.71|Formula: C13H10ClN3O2|Chemical Name: 2-{[6-chloro-3-(²H₃)methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl]methyl}benzonitrile|Smiles: [2H]C([2H])([2H])N1C(=O)N(CC2=CC=CC=C2C#N)C(Cl)=CC1=O|InChiKey: BVUJISIVAHYNLI-FIBGUPNXSA-N|InChi: InChI=1S/C13H10ClN3O2/c1-16-12(18)6-11(14)17(13(16)19)8-10-5-3-2-4-9(10)7-15/h2-6H,8H2,1H3/i1D3|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.|Shelf Life: ≥12 months if stored properly.|Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.|Drug Formulation: To be determined|HS Tariff Code: 382200|Products are for research use only. Not for human use.|

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1-Acetyl-3-o-toluyl-5-fluorouracil is a potent an antineoplastic agent.|Product information|CAS Number: 71861-76-2|Molecular Weight: 290.25|Formula: C14H11FN2O4|Chemical Name: 1-acetyl-5-fluoro-3-(2-methylbenzoyl)-1,2,3,4-tetrahydropyrimidine-2,4-dione|Smiles: CC(=O)N1C=C(F)C(=O)N(C(=O)C2=CC=CC=C2C)C1=O|InChiKey: DRXHAKVGNKHFMB-UHFFFAOYSA-N|InChi: InChI=1S/C14H11FN2O4/c1-8-5-3-4-6-10(8)12(19)17-13(20)11(15)7-16(9(2)18)14(17)21/h3-7H,1-2H3|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.{{D-Cycloserine} site|{D-Cycloserine} Anti-infection|{D-Cycloserine} Protocol|{D-Cycloserine} In stock|{D-Cycloserine} manufacturer|{D-Cycloserine} Epigenetics} |Shelf Life: ≥12 months if stored properly.{{Mirin} MedChemExpress|{Mirin} PI3K/Akt/mTOR|{Mirin} Purity & Documentation|{Mirin} In Vitro|{Mirin} supplier|{Mirin} Autophagy} |Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.PMID:31985186 |Drug Formulation: To be determined|HS Tariff Code: 382200|How to use|In Vivo:|Oral administration of 1-Acetyl-3-o-toluyl-5-fluorouracil demonstrates a remarkable effect on MH134 solid tumors, the effect being more marked than that of subcutaneous administration of 1-Acetyl-3-o-toluyl-5-fluorouracil. Anti-tumor activity of oral administration of 1-Acetyl-3-o-toluyl-5-fluorouracil at a dose of 0.2 mmol/kg/d is comparable to that of subcutaneous administration of 5-fluorouracil at the same dose. The level of decrease in thymus weight and the magnitude of increase of spleen weight following oral administration of 1-Acetyl-3-o-toluyl-5-fluorouracil at any dose are smaller than those by subcutaneous administration of 5-fluorouracil (0.2 mmol/kg/d).|Products are for research use only. Not for human use.|

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Viquidil hydrochloride (Quinotoxine hydrochloride), an isomer of Quinidine, is a cerebral vasodilator agent. Viquidil hydrochloride shows antithrombotic activity.|Product information|CAS Number: 52211-63-9|Molecular Weight: 360.88|Formula: C20H25ClN2O2|Chemical Name: 3-[(3R,4R)-3-ethenylpiperidin-4-yl]-1-(6-methoxyquinolin-4-yl)propan-1-one hydrochloride|Smiles: Cl.{{Fmoc-L-Trp(Boc)-OH} site|{Fmoc-L-Trp(Boc)-OH} {Amino Acid Derivatives}|{Fmoc-L-Trp(Boc)-OH} Technical Information|{Fmoc-L-Trp(Boc)-OH} Description|{Fmoc-L-Trp(Boc)-OH} supplier|{Fmoc-L-Trp(Boc)-OH} Autophagy} COC1=CC2=C(C=CN=C2C=C1)C(=O)CC[C@@H]1CCNC[C@@H]1C=C|InChiKey: YUBRJAHSRSIPKX-LDXVYITESA-N|InChi: InChI=1S/C20H24N2O2.{{Ferritin heavy chain/FTH1 Protein, Human} web|{Ferritin heavy chain/FTH1 Protein, Human} Biological Activity|{Ferritin heavy chain/FTH1 Protein, Human} References|{Ferritin heavy chain/FTH1 Protein, Human} custom synthesis|{Ferritin heavy chain/FTH1 Protein, Human} Epigenetics} ClH/c1-3-14-13-21-10-8-15(14)4-7-20(23)17-9-11-22-19-6-5-16(24-2)12-18(17)19;/h3,5-6,9,11-12,14-15,21H,1,4,7-8,10,13H2,2H3;1H/t14-,15+;/m0.PMID:32529926 /s1|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Solubility: H2O : 15 mg/mL (41.57 mM; Need ultrasonic).|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.|Shelf Life: ≥12 months if stored properly.|Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.|Drug Formulation: To be determined|HS Tariff Code: 382200|How to use|In Vivo:|Viquidil hydrochloride (Quinotoxine hydrochloride) increases the cerebral blood flow in the rabbit considerably.|Products are for research use only. Not for human use.|

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Nordihydrocapsaicin is a capsaicinoid analog and congener of capsaicin in chili peppers.{{Isradipine} MedChemExpress|{Isradipine} Calcium Channel|{Isradipine} Biological Activity|{Isradipine} In Vivo|{Isradipine} supplier|{Isradipine} Autophagy} |Product information|CAS Number: 28789-35-7|Molecular Weight: 293.40|Formula: C17H27NO3|Chemical Name: N-[(4-hydroxy-3-methoxyphenyl)methyl]-7-methyloctanamide|Smiles: COC1=CC(CNC(=O)CCCCCC(C)C)=CC=C1O|InChiKey: VQEONGKQWIFHMN-UHFFFAOYSA-N|InChi: InChI=1S/C17H27NO3/c1-13(2)7-5-4-6-8-17(20)18-12-14-9-10-15(19)16(11-14)21-3/h9-11,13,19H,4-8,12H2,1-3H3,(H,18,20)|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.{{Salinomycin} MedChemExpress|{Salinomycin} Wnt|{Salinomycin} NF-κB|{Salinomycin} Technical Information|{Salinomycin} Formula|{Salinomycin} manufacturer} |Shelf Life: ≥12 months if stored properly.PMID:31985940 |Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.|Drug Formulation: To be determined|HS Tariff Code: 382200|Products are for research use only. Not for human use.|

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[Gln8]-C517 (LH-RH), chicken is an avian hypothalamic peptide, which stimulates release of gonadotropins from anterior pituitary, thus regulating reproductive functions.|Product information|CAS Number: 47922-48-5|Molecular Weight: 1154.23|Formula: C54H71N15O14|Chemical Name: (4S)-5-[(2S)-2-[(carbamoylmethyl)carbamoyl]pyrrolidin-1-yl]-4-[(2S)-2-{2-[(2S)-2-[(2S)-3-hydroxy-2-[(2S)-2-[(2S)-3-(1H-imidazol-5-yl)-2-{[(2S)-5-oxopyrrolidin-2-yl]formamido}propanamido]-3-(1H-indol-3-yl)propanamido]propanamido]-3-(4-hydroxyphenyl)propanamido]acetamido}-4-methylpentanamido]-5-oxopentanamide|Smiles: CC(C)C[C@H](NC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@H](CO)NC(=O)[C@H](CC1=CNC2=CC=CC=C12)NC(=O)[C@H](CC1=CN=CN1)NC(=O)[C@@H]1CCC(=O)N1)C(=O)N[C@@H](CCC(N)=O)C(=O)N1CCC[C@H]1C(=O)NCC(N)=O|InChiKey: WPKQYFUSPONRAT-BXXNOCLASA-N|InChi: InChI=1S/C54H71N15O14/c1-28(2)18-37(49(78)64-36(13-15-43(55)72)54(83)69-17-5-8-42(69)53(82)59-24-44(56)73)63-46(75)25-60-47(76)38(19-29-9-11-32(71)12-10-29)65-52(81)41(26-70)68-50(79)39(20-30-22-58-34-7-4-3-6-33(30)34)66-51(80)40(21-31-23-57-27-61-31)67-48(77)35-14-16-45(74)62-35/h3-4,6-7,9-12,22-23,27-28,35-42,58,70-71H,5,8,13-21,24-26H2,1-2H3,(H2,55,72)(H2,56,73)(H,57,61)(H,59,82)(H,60,76)(H,62,74)(H,63,75)(H,64,78)(H,65,81)(H,66,80)(H,67,77)(H,68,79)/t35-,36-,37-,38-,39-,40-,41-,42-/m0/s1|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.|Shelf Life: ≥12 months if stored properly.|Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.|Drug Formulation: To be determined|HS Tariff Code: 382200|Products are for research use only. Not for human use.|

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Sandramycin ia a cyclic depsipeptide antibiotic isolated from cultured broth of a Nocardioides sp. Sandramycin is also a DNA intercalator that potently binds DNA and is an ADC cytotoxin. Sandramycin is active against Gram-positive bacteria and has potent antitumor activity.|Product information|CAS Number: 100940-65-6|Molecular Weight: 1221.{{SMARCA2/4-IN-2} MedChemExpress|{SMARCA2/4-IN-2} PROTAC|{SMARCA2/4-IN-2} Activator|{SMARCA2/4-IN-2} Protocol|{SMARCA2/4-IN-2} Formula|{SMARCA2/4-IN-2} supplier} 32|Formula: C60H76N12O16|Chemical Name: 3-hydroxy-N-[(3R, 7S, 16S, 23R, 27S, 36S)-23-(3-hydroxyquinoline-2-amido)-8, 11, 28, 31-tetramethyl-2, 6, 9, 12, 15, 22, 26, 29, 32, 35-decaoxo-7, 27-bis(propan-2-yl)-5, 25-dioxa-1, 8, 11, 14, 21, 28, 31, 34-octaazatricyclo[34.4.0.0, ]tetracontan-3-yl]quinoline-2-carboxamide|Smiles: CN1CC(=O)N(C)[C@@H](C(C)C)C(=O)OC[C@@H](NC(=O)C2=NC3=CC=CC=C3C=C2O)C(=O)N2CCCC[C@H]2C(=O)NCC(=O)N(C)CC(=O)N(C)[C@@H](C(C)C)C(=O)OC[C@@H](NC(=O)C2=NC3=CC=CC=C3C=C2O)C(=O)N2CCCC[C@H]2C(=O)NCC1=O|InChiKey: WXIVYIYCEBUEHL-RTQGILJWSA-N|InChi: InChI=1S/C60H76N12O16/c1-33(2)51-59(85)87-31-39(65-55(81)49-43(73)25-35-17-9-11-19-37(35)63-49)57(83)71-23-15-13-21-41(71)53(79)62-28-46(76)68(6)30-48(78)70(8)52(34(3)4)60(86)88-32-40(66-56(82)50-44(74)26-36-18-10-12-20-38(36)64-50)58(84)72-24-16-14-22-42(72)54(80)61-27-45(75)67(5)29-47(77)69(51)7/h9-12,17-20,25-26,33-34,39-42,51-52,73-74H,13-16,21-24,27-32H2,1-8H3,(H,61,80)(H,62,79)(H,65,81)(H,66,82)/t39-,40-,41+,42+,51+,52+/m1/s1|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Solubility: Soluble in DMSO|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.|Shelf Life: ≥360 days if stored properly.|Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.{{Opipramol} MedChemExpress|{Opipramol} Sigma Receptor|{Opipramol} Biological Activity|{Opipramol} In Vivo|{Opipramol} supplier|{Opipramol} Epigenetics} |Drug Formulation: To be determined|HS Tariff Code: 382200|How to use|In Vitro:|Sandramycin has antimicrobial activity wtih MIC values of 0.PMID:32329329 024 μg/mL, 0.012 μg/mL, 0.012 μg/mL, 0.098 μg/mL, 0.024 μg/mL, 12.5 μg/mL and 12.5 μg/mL for Bacillus subtilis (Rec+) A22508-2, B. subtilis (Rec-) A22509-2-2, Staphylocccus aureus 209P-A9497, S. aureus (echinomycin-resistant) A9628, Streptococcus faecalis A96 1 1, Escherichia coli A151 19 and E. coli (actinomycin-sensitive) A21780 (AS-19), respectively. Sandramycin inhibits cancer cells growth of L1210, B16, HCT118, RPMI8226, A431, RKO, SU-DHL6 and SU-DHL10 cells with IC50 values of 0.02 nM, 0.07 nM, 0.8 nM, 3.8 nM, 3.1 nM, 1.3 nM, 5.9 nM and 3.3 nM, respectively.|In Vivo:|Sandramycin (0.0125-1.6 mg/kg; intraperitoneal injection; daily; for 5 days; CDF1 female mice) treatment shows moderately active in vivo against leukemia P388 in mice.|References:|J A Matson, et al. Sandramycin, a Novel Antitumor Antibiotic Produced by a Nocardioides Sp. Production, Isolation, Characterization and Biological Properties. J Antibiot (Tokyo). 1989 Dec;42(12):1763-7.Katsushi Katayama, et al. Total Synthesis of Sandramycin and Its Analogues via a Multicomponent Assemblage. Org Lett. 2014 Jan 17;16(2):428-31.Products are for research use only. Not for human use.|