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| Product | Description | |
|---|---|---|
| Viphi G | Viphi G is a cytotoxic cyclic peptide isolated from Viola philippica, which shows cytotoxic activity to cancer cell lines MM96L, HeLa and BGC-823. Synonyms: Gly-Ser-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Phe-Ile-Pro-Cys-Ile-Ser-Ala-Ile-Ile-Gly-Cys-Ser-Cys-Ser-Asn-Lys-Val-Cys-Tyr-Lys-Asn. Mole weight: 3170.36. |  |
| VIPhyb | VIPhyb is a vasoactive intestinal polypeptide (VIP) receptor antagonist. VIPhyb can inhibit VIP signaling, increase T-cell immunity and downregulate PD1. VIPhyb can inhibit cancer cell proliferation. VIPhyb can reduce inflammatory cytokine expression. VIPhyb can enhance viral clearance. VIPhyb can be used for the researches of cancer, infection and inflammation and immunology, such as non-small cell lung cancer (NSCLC), cytomegalovirus infection and colitis[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 125093-93-8. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P5005. |  |
| Vipivotide tetraxetan | Vipivotide tetraxetan is a human prostate-specific membrane antigen (PSMA)-targeting ligand that binds to PSMA-expressing tumor cells. Vipivotide tetraxetan could be labeled with 177Lu for imaging and detecting tumors. Uses: Vipivotide tetraxetan has been used in prostate cancer research, and is a promising prostate-specific membrane antigen-targeted theranostic agent. Synonyms: PSMA-617; PSMA 617; PSMA617; Glu-NH-CO-NH-Lys[(2-Nal)-Amc-DOTA]. Grade: >98.0%. CAS No. 1702967-37-0. Molecular formula: C49H71N9O16. Mole weight: 1042.14. | |
| Vipivotide tetraxetan | Vipivotide tetraxetan (PSMA-617) is a high potent prostate-specific membrane antigen (PSMA) inhibitor, with a Ki of 0.37 nM. Vipivotide tetraxetan (PSMA-617) is designed consisting of three components: the pharmacophore Glutamate-urea-Lysine, the chelator DOTA able to complex both 68Ga or 177Lu, and a linker connecting these two entities. Glutamate-urea-Lysine is the selective pharmacophore to bind to prostate specific membrane antigen. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PSMA-617. CAS No. 1702967-37-0. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-117410. | |
| Vipivotide tetraxetan Ligand-Linker Conjugate | Vipivotide tetraxetan Ligand-Linker Conjugate (PSMA-617 Ligand-Linker Conjugate) is a complex composed of pharmacophore group Glutamate-urea-Lysine peptide coupling linker, which can be used to synthesize Vipivotide tetraxetan (PSMA-617). Glutamate-urea-Lysine selectively binds to prostate-specific membrane antigen (PSMA)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PSMA-617 Ligand-Linker Conjugate. CAS No. 1703768-74-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-43869. | |
| Vipoglanstat | Vipoglanstat (BI 1029539), a carboxamide, is a potent and selective, non-peptide and orally active small molecular inhibitor of human prostaglandin E synthase 1 (mPGES-1). Vipoglanstat also has anti-inflammatory activity[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BI 1029539; GS-248; OX-MPI. CAS No. 1360622-01-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147416. | |
| VIR-165 | VIR-165 is a modified form of virus inhibitory peptide (VIRIP) that binds the fusion peptide of the gp41 subunit and prevents its insertion into the target membrane. It can inhibit a wide variety of human immunodeficiency virus type 1 (HIV-1) strains. Synonyms: Mutant of Virus-inhibitory peptide (VIRIP); NH2-Leu-Glu-Ala-Ile-Pro-Cys(x1)-Ser-Ile-Pro-Pro-Cys(x1)-Phe-Ala-Phe-Asn-Lys-Pro-Phe-Val-Phe-COOH. Molecular formula: C109H158N22O25S2. Mole weight: 2240.6999999999998. | |
| Viral polymerase-IN-1 hydrochloride | Viral polymerase-IN-1 hydrochloride, a derivative of Gemcitabine, effectively inhibits influenza A and B virus infections with IC90 values between 11.4 and 15.9 μM, and shows activity against SARS-CoV-2 infection by interfering with viral RNA replication/transcription within cells. Category: Active pharmaceutical ingredients. CAS No. 2367587-02-6. Product ID: API2367587026. Molecular formula: C15H16ClF2N5O5. Mole weight: 419.77. |  |
| Viramidine Hydrochloride | Viramidine Hydrochloride. Alternative Names: 1-β-D-Ribofuranosyl-1H-1,2,4-triazole-3-carboximidamide Monohydrochloride. CAS No. 40372-00-7. Purity: 98%. Product ID: ACM40372007. Molecular formula: C8H14ClN5O4. Mole weight: 279.68. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Viranamycin A | It is produced by the strain of Str. sp. CH 41. It can inhibit the growth of murine leukemia cell P388 with IC50 of 5.8 ng/mL, and it can also inhibit KB human multi-squamous cell carcinoma cells with IC50 of 6.4 ng/mL. Synonyms: Concanamycin A, 23-O-(3-carboxy-1-oxo-2-propenyl)-23-O-de[4-O-(aminocarbonyl)-2,6-dideoxy-b-D-arabino-hexopyranosyl]-25-de(1-propenyl)-25-methyl-. CAS No. 139595-03-2. Molecular formula: C41H64O13. Mole weight: 764.94. | |
| Viranamycin B | It is produced by the strain of Str. sp. CH 41. It can inhibit the growth of murine leukemia cell P388 with IC50 of 2.8 ng/mL, and it can also inhibit KB human multi-squamous cell carcinoma cells with IC50 of 1.9 ng/mL. Synonyms: Concanamycin A, 25-de(1-propenyl)-25-methyl-. CAS No. 139595-04-3. Molecular formula: C44H73NO14. Mole weight: 840.05. | |
| Virantmycin | It is produced by the strain of Str. nitrosporeus AM-2722. It has antiviral effect. It inhibits four RNA viruses and four DNA viruses with MIC (μg/mL) of 0.008-0.04 and 0.005-0.03, respectively. It has weak antifungal effect. Synonyms: 6-Quinolinecarboxylic acid, 3-chloro-2-(3,4-dimethyl-3-penten-1-yl)-1,2,3,4-tetrahydro-2-(methoxymethyl)-, (2R,3R)-; NSC 374127; 6-Quinolinecarboxylic acid, 3-chloro-2-(3,4-dimethyl-3-pentenyl)-1,2,3,4-tetrahydro-2-(methoxymethyl)-, (2R-cis)-; (-)-Virantmycin. Grade: 99%. CAS No. 76417-04-4. Molecular formula: C19H26C1NO3. Mole weight: 351.87. | |
| VIRE_HELVI Virescein | VIRE_HELVI Virescein is an antibacterial peptide isolated from Helioth is virescens. Synonyms: Virescein (Insects, animals); Gly-Lys-Ile-Pro-Ile-Gly-Ala-Ile-Lys-Lys-Ala-Gly-Lys-Ala-Ile-Gly-Lys-Gly-Leu-Arg-Ala-Val-Asn-Ile-Ala-Ser-Thr-Ala-His-Asp-Val-Tyr-Thr-Phe-Phe-Lys-Pro-Lys-Lys-Arg-His. Molecular formula: C202H336N60O49. Mole weight: 4389.26. | |
| Virensic acid | It is a lichen acid with enzyme inhibitory potential. Synonyms: 11H-Dibenzo[b,e][1,4]dioxepin-7-carboxylic acid, 4-formyl-3,8-dihydroxy-1,6,9-trimethyl-11-oxo-; 10-formyl-3,9-dihydroxy-1,4,7-trimethyl-6-oxobenzo[b][1,4]benzodioxepine-2-carboxylic acid; Granulatine; NSC 685587. CAS No. 668-14-4. Molecular formula: C18H14O8. Mole weight: 358.30. | |
| Viresin | Viresin is an antibacterial protein isolated from immune hemolymph of Helioth is virescens pupae. Viresin showed antibacterial activity against several Gram-negative bacteria including E. cloacae but not against Gram-positive bacteria. Synonyms: Tyr-Asp-Asn-Val-Asn-Leu-Asp-Glu-Ile-Leu-Ala-Asn-Asp-Arg-Leu-Leu-Val-Pro-Tyr-Ile-Lys-Cys-Leu-Leu-Asp-Glu-Gly-Lys-Lys-Ala-Pro-Asp-Ala-Lys-Glu-Leu-Lys-Glu-His-Ile-ArgX-Ala-Leu. Molecular formula: C221H361N59O66S. Mole weight: 5062.06. | |
| Virgaureagenin G | Virgaureagenin G. Group: Biochemicals. CAS No. 22338-71-2. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| Virginiamycin | Virginiamycin complex contains two streptogramin antibiotics, virginiamycin M1 (75%) and virginiamycin S1 (25%). It is an antibiotic used primarily in the treatment of staphylococcal infections, and to a less extent streptococcal infections. Uses: Anti-bacterial agents. Synonyms: Pristinamycin. CAS No. 11006-76-1. Molecular formula: C71H84N10O17. Mole weight: 1349.48. | |
| Virginiamycin B | Pristinamycin IA is an ester peptide antibiotic produced by Str. pristinaespiralis 5647 (NRRL 2958). Activity against gram-positive bacteria. Synonyms: Mikamycin B; Ostreogrycin B; Pristinamycin IA; Streptogramin B; Syncothrecin B1; Synergistin B; Vernamycin Balpha; Antibiotic PA 114B. Grade: 95%. CAS No. 3131-3-1. Molecular formula: C45H54N8O10. Mole weight: 866.96. | |
| Virginiamycin B | Virginiamycin B is a depsipeptide antibiotic co-produced with ostreogrycin A and used as a synergistic mixture. Virginiamycin B, also known as ostreogrycin B and streptogramin B among other synonyms, was discovered independently and named by several groups leading to considerable confusion in the literature. Viriginiamycin B acts as a synergist binding to the conformational change in the peptidyl transferase centre of the 50S ribosome induced by ostreogrycin A. Group: Biochemicals. Grades: Highly Purified. CAS No. 3131-3-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Virginiamycin Complex | Virginiamycin complex is defined as a mixture of 75% virginamycin M1 (ostreogrycin A) and 25% virginiamycin S1 and the less abundant S analogs. As the two major components have quite different solubilities these proportions are not readily achieved or used. The individual components are isolated and re-combined to provide the defined components of virginiamycin complex. The structure composition of the complex is important as Virginiamycin S1 acts a synergist, binding to the conformational change of the peptidyl transferase center of the 50S ribosome induced by ostreogrycin A. Group: Biochemicals. Alternative Names: Cebin V, Eskalin V, Eskamicin, Stafac, Stephylomycin, Mikamycin, Ostreogrycin, Patricin, Pristinamycin, Streptogramin, Vernamycin. Grades: Highly Purified. CAS No. 11006-76-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Virginiamycin M1 | Macrolactone antibiotic. Antibacterial; growth promotant. Group: Biochemicals. Grades: Highly Purified. CAS No. 21411-53-0. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Virginiamycin S1 | It is a depsipeptide antibiotic produced by the strain of Str. virginiae and Str. virginiae var. sp. It has anti-gram-positive bacteria and mycobacterium effects, and the antibacterial activity of component M of Virginiamycin against cocci is stronger than component S, while the activity is stronger than component M. Synonyms: Staphylomycin S; Staphylomycin S1; Antibiotic 1754Z3B; Virginiamycin factor S; NSC177858; Stephylomycin; Eskamicin; Cebin V; Factor S; Glycine, N-[(3-hydroxy-2-pyridinyl)carbonyl]-L-threonyl-D-2-aminobutanoyl-L-prolyl-N-methyl-L-phenylalanyl-4-oxo-L-2-piperidinecarbonyl-L-2-phenyl-, r-lactone. Grade: >99% by HPLC. CAS No. 23152-29-6. Molecular formula: C43H49N7O10. Mole weight: 823.89. | |
| Virginiamycin S1 | Virginiamycin S1 is a cyclic hexadepsipeptide antibiotic, inhibits bacterial protein synthesis at the level of aminoacyl-tRNA binding and peptide bond formation. Virginiamycin S1 belongs to the type B compounds in the streptogramin family and is produced by Streptomyces virginiae, shows a strong bactericidal activity against a wide range of Gram-positive bacteria. Virginiamycin S1 together with virginiamycin M1 is more effective in treat multidrug-resistant bacterial infections[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 23152-29-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N6680. | |
| Virginiamycin S1 | Virginiamycin S1 is a main component of virginiamycin preparations. Virginiamycin S1 is one of a family of depsipeptide antibiotic co-produced with ostreogrycin A and used as a synergistic mixture. Virginiamycin S1 also known as Staphylomycin S and Factor S, among other synonyms were discovered independently and named by several groups leading to considerable confusion in the literature. Virginiamycin S1 acts a synergist binding to the conformational change induced by ostreogrycin A of the peptidyl transferase centre of the 50S ribosome. Virginiamycin S1 differs from virginiamycin B in lacking the dimethylamino moiety on the phenyl ring. Group: Biochemicals. Alternative Names: Staphylomycin S, PA 114B2, Antibiotic 899, Antibiotic PA 114B2, Antibiotic 1745Z3B, Factor S. Grades: Highly Purified. CAS No. 23152-29-6. Pack Sizes: 5mg. Molecular Formula: C43H49N7O10, Molecular Weight: 823.89. US Biological Life Sciences. | Worldwide |
| Virginiamycin S2 | It is a depsipeptide antibiotic produced by the strain of Str. virginiae and Str. virginiae var. sp. It has anti-gram-positive bacteria and mycobacterium effects, and the antibacterial activity of component M of Virginiamycin against cocci is stronger than component S, while the activity is stronger than component M. Synonyms: Staphylomycin-S2; 4-L-Phenylalanine-5-(cis-4-hydroxy-L-2-piperidinecarboxylic acid)virginiamycin S1; N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Abu-L-Pro-L-Phe-[(4R)-4-hydroxy-L-pipecoloyl]-L-phenyl-Gly-]; N-[(3-Hydroxy-2-pyridyl)carbonyl]-cyclo[L-Thr*-D-Abu-L-Pro-L-Phe-4β-hydroxy-L-Hpr-L-phenyl-Gly-]. CAS No. 33477-38-2. Molecular formula: C42H49N7O10. Mole weight: 811.88. | |
| Virginiamycin S3 | It is a depsipeptide antibiotic produced by the strain of Str. virginiae and Str. virginiae var. sp. It has anti-gram-positive bacteria and mycobacterium effects, and the antibacterial activity of component M of Virginiamycin against cocci is stronger than component S, while the activity is stronger than component M. Synonyms: Staphylomycin S3; Virginiamycin S1, 5-(5-hydroxy-4-oxo-L-2-piperidinecarboxylic acid)-; N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Abu-L-Pro-N-methyl-L-Phe-4-oxo-5-hydroxy-L-pipecoloyl-L-phenyl-Gly-]. CAS No. 33477-39-3. Molecular formula: C43H49N7O11. Mole weight: 839.89. | |
| Viridicatin | Viridicatin is a fungal metabolite produced by several species of Penicillium and formed by the rearrangement of the benzodiazepine, cyclopenin. Viridicatin exhibits potent selective activity against Mycobacterium tuberculosis but is inactive against most other bacteria. Group: Biochemicals. Alternative Names: 2,3-dihydroxy-4-phenylquinoline. Grades: Highly Purified. CAS No. 129-24-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Viridicatin | It is a quinoline aromatic antibiotic produced by the strain of Pen. viridicatum, Pen. cyclopium SM-72 and Pen. puberulum. It has anti-gram-positive bacteria and mycobacteria effects. Synonyms: 2,3-dihydroxy-4-phenylquinoline; 2(1H)-Quinolinone, 3-hydroxy-4-phenyl-. Grade: >99% by HPLC. CAS No. 129-24-8. Molecular formula: C15H11NO2. Mole weight: 237.25. | |
| Viridicatol | Viridicatol is a fungal metabolite found in various Penicillium species as well as Phoma. It suppresses the expression of COX-2 and inducible nitric oxide synthase (iNOS) and inhibits production of nitric oxide and prostaglandin E2 (PGE2) in LPS-stimulated RAW 264.7 and BV2 cells. Synonyms: 2(1H)-Quinolinone, 3-hydroxy-4-(3-hydroxyphenyl)-; Carbostyril, 3-hydroxy-4-(m-hydroxyphenyl)-; 3-hydroxy-4-(3-hydroxyphenyl)carbostyril; 4-(3-Hydroxyphenyl)-2,3-quinolinediol. Grade: ≥95%. CAS No. 14484-44-7. Molecular formula: C15H11NO3. Mole weight: 253.25. | |
| Viridicatumtoxin | A tetracycline-like metabolite produced by several species of penicillium. It causes myocardial deterioration, renal tubule necrosis and spleen atrophy. It is a mycotoxin and a potent antibacterial with activity against S. Aureus including MRSA and QRSA strains. Synonyms: NSC 159628; viridicatumtoxin A; (1R,7'aR,11'aR,12'R)-rel-(-)-7',7'a,8',11',11'a,12'-hexahydro-5',6',7'a,10',11'a,12'-hexahydroxy-3'-methoxy-2,6,6-trimethyl-7',8'-dioxo-spiro[2-cyclohexene-1,2'(1'H)-cyclopenta[de]naphthacene]-9'-carboxamide; (2'α,7'aβ,11'aβ,12'β)-(-)-7',7'a,8',11',11'a,12'-Hexahydro-5',6',7'a,10',11'a,12'-hexahydroxy-3'-methoxy-2,6,6-trimethyl-7',8'-dioxo-spiro[2-cyclohexene-1,2'(1'H)-cyclopenta[de]naphthacene]-9'-carboxamide. Grade: >98% by HPLC. CAS No. 39277-41-3. Molecular formula: C30H31NO10. Mole weight: 565.57. | |
| viridiflorene synthase | Viridiflorene is the only product of this enzyme from Solanum lycopersicum. Group: Enzymes. Synonyms: TPS31. Enzyme Commission Number: EC 4.2.3.88. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5251; viridiflorene synthase; EC 4.2.3.88; TPS31. Cat No: EXWM-5251. |  |
| Viridifloric acid | Viridifloric acid. Alternative Names: Viridifloric acid, CCRIS 9200, (2r,3r)-2,3-dihydroxy-2-(propan-2-yl)butanoic acid, Butanoic acid, 2,3-dihydroxy-2-(1-methylethyl)-, (R-(R*,R*))-, 17233-93-1, AC1L4MJE, AC1Q5QYA, Oprea1_244262, CTK4D4201, KST-1A2597, KST-1A2598, AR-1A2817, AR-1A2818, AKOS006331598, AG-K-77595, LS-188470, Butanoic acid,2,3-dihydroxy-2-(1-methylethyl)-, (2R,3R)-, (2R)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoic acid, Butanoicacid, 2,3-dihydroxy-2-(1-methylethyl)-, [R-(R*,R*)]-; Butyric acid,2,3-dihydroxy-2-isopropyl-, (2R,3R)- (8CI); (+)-(2R,3R)-Viridifloric acid;(+)-Viridifloric acid; (2R,3R)-Viridifloric acid; Viridifloric acid, (+)-;Viridiflorinoic acid, (+)-. CAS No. 17233-93-1. Purity: 96%. Product ID: ACM17233931. Molecular formula: C7H14O4. Mole weight: 162.18. IUPAC Name: (2R)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Viridin | It is a steroidal antibiotic produced by the strain of Gliocladium virens. It has anti-fungal and gram-positive bacterial effects. Synonyms: (1S-(1alpha,2alpha,11balpha))-1,7,8,11b-Tetrahydro-1-hydroxy-2-methoxy-11b-methylcyclopenta(7,8)phenanthro(10,1-bc)furan-3,6,9(2H)-trione; 18-Norandrosta-5,8,11,13-tetraeno(6,5,4-bc)furan-3,7,17-trione, 1-hydroxy-2-methoxy-, (1beta,2beta)-; Cyclopenta(7,8)phenanthro(10,1-bc)furan-3,6,9(2H)-trione, 1,7,8,11b-tetrahydro-1-hydroxy-2-methoxy-11b-methyl-, (1S,2R,11bS)-. CAS No. 3306-52-3. Molecular formula: C20H16O6. Mole weight: 352.34. | |
| Viridiol | Steroidal antibiotic. Belongs to the Viridin family, including Wortmannin. Antifungal. Phytotoxin. Shows necrotic activity on plants. Phosphatidylinositol 3-kinase (PI3K) inhibitor. Group: Biochemicals. Alternative Names: NSC 658706, 3beta-Alcohol-Viridin. Grades: Highly Purified. CAS No. 23820-80-6. Pack Sizes: 250ug, 1mg. Molecular Formula: C20H18O6. US Biological Life Sciences. | Worldwide |
| Viridomycin F | It is a viridomycin antibiotic produced by the strain of Streptomyces sp. K96-0188. It has weak insecticidal and nematocidal activity. It also has weak activity against Piricularia oryzae and Acholeplasma laidlawii. Synonyms: Antibiotic K 96-0188. CAS No. 221394-79-2. Molecular formula: C21H14N3O9Fe. Mole weight: 508.20. | |
| Virodhamine | Virodhamine. Alternative Names: 2-Aminoethyl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate. CAS No. 287937-12-6. Product ID: FFC-AR-287937126. Molecular formula: C22H37NO2. Mole weight: 347.53. IUPAC Name: 2-aminoethyl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Virstatin | Virstatin is an inhibitor of the virulence transcriptional activator ToxT of V. cholerae. It prevents expression of the two major V. cholerae virulence factors, cholera toxin (CT) and the toxin coregulated pilus, by inhibiting ToxT. Synonyms: Isodibut; 4-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-butyric acid; 4-(1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)butanoic acid; 4-(N-(1,8-naphthalimide))-n-butyric acid; 1,3-Dioxo-1H-benz(de)isoquinoline-2(3H)-butanoic acid. Grade: ≥98%. CAS No. 88909-96-0. Molecular formula: C16H13NO4. Mole weight: 283.28. | |
| Virustomycin A | Virustomycin A is a 18-membered macrolide antibiotic originally isolated from Streptomyces sp. AM-2604. It is effective against infectious and plant pathogenic fungi. It is active against trichomonads and various RNA and DNA viruses. Synonyms: AM 2604A; Antibiotic AM 2604A; [2R-[2R*[1S*[2R*,4R*,5S*,6R*(E)],2R*,3S*],3S*,4E,6E,9R*,10S*,11S*,12R*,13R*,14E,16Z]]-2-[3-(11-Ethyl-10,12-dihydroxy-3,17-dimethoxy-7,9,13,15-tetramethyl-18-oxooxacyclooctadeca-4,6,14,16-tetraen-2-yl)-2-hydroxy-1-methylbutyl]tetrahydro-2-hydroxy-5-methyl-6-(1-propenyl)-2H-pyran-4-yl Ester 4-[(2-hydroxy-5-oxo-1-cyclopenten-1-yl)amino]-4-oxo-2-butenoic Acid; 23-O-De(4-O-aminocarbonyl-2,6-dideoxy-β-D-arabino-hexopyranosyl)-23-O-[4-[(2-hydroxy-5-oxo-1-cyclopenten-1-yl)amino]-1,4-dioxo-2-butenyl]concanamycin A. Grade: ≥98%. CAS No. 84777-85-5. Molecular formula: C48H71NO14. Mole weight: 886.08. | |
| VIS-410 | VIS-410 is an antibody inhibitor targeting the stem region of hemagglutinin (HA). VIS-410 inhibits influenza virus replication by blocking HA-mediated membrane fusion. VIS-410 exhibits broad-spectrum neutralization against influenza A viruses with group 1 and group 2 hemagglutinins, including subtypes such as H1N1, H3N2, H5N1, and H7N9 (H5N1 IC50 = 1.5 μg/mL). VIS-410 is applicable to research related to influenza A virus infection[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2043950-09-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P991059. | |
| Viscidulin I | Viscidulin I is isolated from the roots of Scutellaria viscidula Bge. Synonyms: 4H-1-Benzopyran-4-one, 2-(2,6-dihydroxyphenyl)-3,5,7-trihydroxy-; 5,7,2',6'-Tetrahydroxyflavonol. Grade: 98%. CAS No. 92519-95-4. Molecular formula: C15H10O7. Mole weight: 302.2. | |
| Viscidulin III | Viscidulin III isolated from the roots of Scutellaria viscidula Bge. It was more effective than baicalein (23.0 microM) which reportedly inhibits the proliferation of some cancer cell lines. Synonyms: ganhuangenin; 2-(3,6-dihydroxy-2-methoxyphenyl)-5,7-dihydroxy-8-methoxychromen-4-one. Grade: 0.98. CAS No. 92519-91-0. Molecular formula: C17H14O8. Mole weight: 346.3. | |
| Viscotoxin 1-PS | Viscotoxin 1-PS is a small protein that is toxic to many cell types. It belongs to the thionin family and is isolated from Viscum album L. Synonyms: Lys-Ser-Cys-Cys-Pro-Asn-Thr-Thr-Gly-Arg-Asn-Ile-Tyr-Asn-Thr-Cys-Arg-Phe-Gly-Gly-Gly-Ser-Arg-Glu-Val-Cys-Ala-Arg-Ile-Ser-Gly-Cys-Lys-Ile-Ile-Ser-Ala-Ser-Thr-Cys-Pro-Ser-Asp-Tyr-Pro-Lys. | |
| Viscotoxin A1 | Viscotoxin A1 is a small protein that is toxic to many cell types. It belongs to the thionin family and is isolated from Viscum album L. | |
| Viscotoxin A2 | Viscotoxin A2 is a small protein that is toxic to many cell types. It belongs to the thionin family and is isolated from Viscum album L. Synonyms: Lys-Ser-Cys-Cys-Pro-Asn-Thr-Thr-Gly-Arg-Asn-Ile-Tyr-Asn-Thr-Cys-Arg-Phe-Gly-Gly-Gly-Ser-Arg-Gln-Val-Cys-Ala-Ser-Leu-Ser-Gly-Cys-Lys-Ile-Ile-Ser-Ala-Ser-Thr-Cys-Pro-Ser-Asp-Tyr-Pro-Lys. | |
| Viscotoxin A3 | Viscotoxin A3 is a small protein that is toxic to many cell types. It belongs to the thionin family and is isolated from Viscum album L. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Lys-Ser-Cys-Cys-Pro-Asn-Thr-Thr-Gly-Arg-Asn-Ile-Tyr-Asn-Ala-Cys-Arg-Leu-Thr-Gly-Ala-Pro-Arg-Pro-Thr-Cys-Ala-Lys-Leu-Ser-Gly-Cys-Lys-Ile-Ile-Ser-Gly-Ser-Thr-Cys-Pro-Ser-Asp-Tyr-Pro-Lys. Molecular formula: C201H334N62O64S6. Mole weight: 4835.6. | |
| Viscotoxin B | Viscotoxin B is a small protein that is toxic to many cell types. It belongs to the thionin family and is isolated from Viscum album L. Synonyms: H-Lys-Ser-Cys(1)-Cys(2)-Pro-Asn-Thr-Thr-Gly-Arg-Asn-Ile-Tyr-Asn-Thr-Cys(3)-Arg-Leu-Gly-Gly-Gly-Ser-Arg-Glu-Arg-Cys(3)-Ala-Ser-Leu-Ser-Gly-Cys(2)-Lys-Ile-Ile-Ser-Ala-Ser-Thr-Cys(1)-Pro-Ser-Asp-Tyr-Pro-Lys-OH. CAS No. 11063-16-4. Molecular formula: C197H322N64O67S6. Mole weight: 4851. | |
| Viscotoxin B2 | Viscotoxin B2 is a small protein that is toxic to many cell types. It belongs to the thionin family and is isolated from Viscum album L. | |
| Viscotoxin C1 | Viscotoxin C1 is a small protein that is toxic to many cell types. It belongs to the thionin family and is isolated from Viscum album L. Synonyms: Lys-Ser-Cys-Cys-Pro-Asn-Thr-Thr-Gly-Arg-Asn-Ile-Tyr-Asn-Thr-Cys-Arg-Phe-Ala-Gly-Gly-Ser-Arg-Glu-Arg-Cys-Ala-Lys-Leu-Ser-Gly-Cys-Lys-Ile-Ile-Ser-Ala-Ser-Thr-Cys-Pro-Ser-Asp-Tyr-Pro-Lys. Molecular formula: C204H335N65O66S6. Mole weight: 4946.66. | |
| Visilizumab | Visilizumab (Anti-Human CD3E Recombinant Antibody) is a humanized low-Fc receptor binding anti-CD3 monoclonal IgG2 antibody. Visilizumab can be used for ulcerative colitis and Crohn's disease research[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Anti-Human CD3E Recombinant Antibody; HuM291. CAS No. 219716-33-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99332. | |
| Vismodegib | Vismodegib (GDC-0449) is a BBB-permeable and orally active hedgehog pathway inhibitor with an IC50 of 3 nM. Vismodegib also inhibits P-gp, ABCG2 with IC50 values of 3.0 μM and 1.4 μM, respectively[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GDC-0449. CAS No. 879085-55-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10440. | |
| Vismodegib-d4 | Vismodegib-d4. Group: Biochemicals. Alternative Names: GDC 0449-d4; 2-Chloro-N-[4-chloro-3-(2-pyridinyl)phenyl]-4-(methylsulfonyl)-benzamide-d4. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C19H10D4Cl2N2O3S, Molecular Weight: 425.3. US Biological Life Sciences. | Worldwide |
| Vismodegib-[d4] | Vismodegib-[d4] is the labelled analogue of Vismodegib, which has been found to inhibit Hh signaling and could probably be effective in anticancer studies. Synonyms: Vismodegib D4; 2-Chloro-N-[4-chloro-3-(2-pyridinyl)phenyl]-4-(methylsulfonyl)-benzamide-d4. Grade: 95% by HPLC; 98% atom D. CAS No. 1450990-33-6. Molecular formula: C19H10D4Cl2N2O3S. Mole weight: 425.32. | |
| Vismodegib (GDC-0449) | Vismodegib (GDC-0449) is a potent, novel and specific hedgehog inhibitor with IC50 of 3 nM and also inhibits P-gp with IC50 of 3.0 μM in a cell-free assay. Group: Inhibitors. Alternative Names: GDC-0449. CAS No. 879085-55-9. Pack Sizes: 5mg. Product ID: S1082. Formula: C19H14Cl2N2O3S. Smiles: CS(=O)(=O)C1=CC(=C(C=C1)C(=O)NC2=CC(=C(C=C2)Cl)C3=CC=CC=N3)Cl. Storage Conditions: 2 years -80 in solvent. |  United States; Europe |
| Vismodegib Impurity 1 | Vismodegib Impurity 1. Uses: For analytical and research use. CAS No. 1121585-09-8. Molecular formula: C8H6Cl2O4S. Mole weight: 269.1. Catalog: APB1121585098. |  |
| Vismodegib Impurity 10 | Vismodegib Impurity 10. Uses: For analytical and research use. CAS No. 63503-60-6. Molecular formula: C6H6BClO2. Mole weight: 156.4. Catalog: APB63503606. | |
| Vismodegib Impurity 11 | Vismodegib Impurity 11. Uses: For analytical and research use. CAS No. 1679-18-1. Molecular formula: C6H6BClO2. Mole weight: 156.4. Catalog: APB1679181. | |
| Vismodegib Impurity 12 | Vismodegib Impurity 12. Uses: For analytical and research use. CAS No. 4381-32-2. Molecular formula: C11H8ClN. Mole weight: 189.6. Catalog: APB4381322. | |
| Vismodegib Impurity 13 | Vismodegib Impurity 13. Uses: For analytical and research use. CAS No. 5957-85-7. Molecular formula: C11H8ClN. Mole weight: 189.6. Catalog: APB5957857. | |
| Vismodegib Impurity 14 | Vismodegib Impurity 14. Uses: For analytical and research use. CAS No. 5969-83-5. Molecular formula: C11H8ClN. Mole weight: 189.7. Catalog: APB5969835. | |
| Vismodegib Impurity 15 | Vismodegib Impurity 15. Uses: For analytical and research use. CAS No. 1922106-89-5. Molecular formula: C11H7ClN2O2. Mole weight: 234.6. Catalog: APB1922106895. | |
| Vismodegib Impurity 16 | Vismodegib Impurity 16. Uses: For analytical and research use. Molecular formula: C11H6ClN3O4. Mole weight: 279.6. Catalog: APB000010. | |
| Vismodegib Impurity 17 | Vismodegib Impurity 17. Uses: For analytical and research use. CAS No. 867333-29-7. Molecular formula: C6H5BClNO4. Mole weight: 201.4. Catalog: APB867333297. | |
| Vismodegib Impurity 18 | Vismodegib Impurity 18. Uses: For analytical and research use. CAS No. 1562430-93-6. Molecular formula: C11H7ClN2O2. Mole weight: 234.6. Catalog: APB1562430936. | |
| Vismodegib Impurity 19 | Vismodegib Impurity 19. Uses: For analytical and research use. Molecular formula: C11H6ClN3O4. Mole weight: 279.6. Catalog: APB000011. | |
| Vismodegib Impurity 2 | Vismodegib Impurity 2. Uses: For analytical and research use. CAS No. 118939-22-3. Molecular formula: C8H6Cl2O4S. Mole weight: 269.1. Catalog: APB118939223. | |
| Vismodegib Impurity 20 | Vismodegib Impurity 20. Uses: For analytical and research use. Molecular formula: C11H6ClN3O4. Mole weight: 279.6. Catalog: APB000012. | |
| Vismodegib Impurity 21 | Vismodegib Impurity 21. Uses: For analytical and research use. CAS No. 25784-91-2. Molecular formula: C7H3Cl2NO3. Mole weight: 220. Catalog: APB25784912. | |
| Vismodegib Impurity 22 | Vismodegib Impurity 22. Uses: For analytical and research use. CAS No. 23082-50-0. Molecular formula: C8H6ClNO3. Mole weight: 199.6. Catalog: APB23082500. | |
| Vismodegib Impurity 23 | Vismodegib Impurity 23. Uses: For analytical and research use. CAS No. 2497-91-8. Molecular formula: C7H3ClN2O6. Mole weight: 246.6. Catalog: APB2497918. | |
| Vismodegib Impurity 24 | Vismodegib Impurity 24. Uses: For analytical and research use. Molecular formula: C11H7ClN2O2. Mole weight: 234.6. Catalog: APB000013. | |
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