| Cat. No. |
Product Name / Activity |
| 2163 |
Z-VAD-FMK |
| Cell-permeable, irreversible caspase inhibitor |
| 6654 |
VAS 2870 |
| NADPH oxidase (Nox) inhibitor |
| 6261 |
VCP 171 New |
| Postitive allosteric modulator (PAM) of A1 receptors; also allosteric partial agonist in absence of orthosteric agonist |
| 6160 |
VE 821 |
| High affinity and selective ATP-competitive ATR inhibitor |
| 3803 |
VER 155008 |
| Hsp70 inhibitor |
| 7104 |
VH 032 amide-PEG1-acid New |
| VHL ligand with PEG linker and terminal acid for onward chemistry |
| 6879 |
VH 032 amide-PEG1-amine |
| VHL ligand with PEG linker and terminal amine for onward chemistry |
| 6684 |
VH 032 amide-PEG2-alkyne |
| VHL ligand with PEG linker and terminal alkyne for onward chemistry |
| 6907 |
VH 032 amide-PEG2-amine |
| VHL ligand with PEG linker and terminal amine for onward chemistry |
| 6679 |
VH 032 amide-PEG3-acid |
| VHL ligand with PEG linker and terminal acid for onward chemistry |
| 6463 |
VH 032 amide-PEG3-amine |
| VHL ligand with PEG linker and terminal amine for onward chemistry |
| 6464 |
VH 032 amide-PEG4-amine |
| VHL ligand with PEG linker and terminal amine for onward chemistry |
| 7105 |
VH 032 amide-PEG5-acid New |
| VHL ligand with PEG linker and terminal acid for onward chemistry |
| 6880 |
VH 032 amide-alkylC10-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 7106 |
VH 032 amide-alkylC2-acid New |
| VHL ligand with alkyl linker and terminal acid for onward chemistry |
| 6852 |
VH 032 amide-alkylC2-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 7216 |
VH 032 amide-alkylC3-acid New |
| VHL ligand with alkyl linker and terminal acid for onward chemistry |
| 7073 |
VH 032 amide-alkylC3-amine New |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 6680 |
VH 032 amide-alkylC4-acid |
| VHL ligand with alkyl linker and terminal acid for onward chemistry |
| 6465 |
VH 032 amide-alkylC4-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 6985 |
VH 032 amide-alkylC5-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 7107 |
VH 032 amide-alkylC6-acid |
| VHL ligand with alkyl linker and terminal acid for onward chemistry |
| 6853 |
VH 032 amide-alkylC6-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 7074 |
VH 032 amide-alkylC7-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 7108 |
VH 032 amide-alkylC8-acid |
| VHL ligand with alkyl linker and terminal acid for onward chemistry |
| 6890 |
VH 032 amide-alkylC8-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 6909 |
VH 032 phenol-alkylC4-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 6910 |
VH 032 phenol-alkylC6-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 6462 |
VH 032, amine |
| Functionalized VHL ligand for PROTACs |
| 6911 |
VH 032, phenol |
| Hydroxyl functionalized VHL ligand |
| 6683 |
VH 032, propargyl |
| Alkyne-functionalized VH 032; 'click' VHL ligand for PROTACs |
| 7293 |
VH 101 phenol-alkylC4-amine New |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 7294 |
VH 101 phenol-alkylC6-amine New |
| VHL ligand with alkyl linker and terminal amine for onward chemistry |
| 6952 |
VH 101, phenol |
| Hydroxyl functionalized VHL ligand |
| 6156 |
VH 298 |
| High-affinity inhibitor of VHL |
| 1905 |
VIP (6-28) (human, rat, porcine, bovine) |
| VIP receptor antagonist |
| 1182 |
VIP (guinea pig) |
| Involved in neurotransmission and smooth muscle relaxation |
| 1911 |
VIP (human, rat, mouse, rabbit, canine, porcine) |
| Involved in neurotransmission and smooth muscle relaxation |
| 3054 |
[D-p-Cl-Phe6,Leu17]-VIP |
| Selective VIP receptor antagonist |
| 3392 |
VKGILS-NH2 |
| Control peptide for SLIGKV-NH2 (Cat. No. 3010) |
| 3591 |
VO-OHpic |
| Potent PTEN inhibitor |
| 3127 |
d[Leu4,Lys8]-VP |
| Selective V1B agonist |
| 4195 |
VPC 23019 |
| S1P1 and S1P3 antagonist |
| 5563 |
VTP 27999 trifluoroacetate |
| Highly potent and selective renin inhibitor |
| 6877 |
VU 0134992 |
| Kir4.1 blocker |
| 3248 |
VU 0155041 |
| Potent positive allosteric modulator of mGlu4 receptors |
| 3311 |
VU 0155041 sodium salt |
| Potent positive allosteric modulator of mGlu4 receptors; sodium salt of VU 0155041 (Cat. No. 3248) |
| 3575 |
VU 0155069 |
| Potent and selective PLD1 inhibitor |
| 3634 |
VU 0238429 |
| Selective positive allosteric modulator of M5 receptors |
| 3888 |
VU 0240551 |
| KCC2 inhibitor |
| 3727 |
VU 0255035 |
| Highly selective M1 antagonist |
| 4381 |
VU 0285683 |
| Negative allosteric modulator of mGlu5 receptors |
| 4295 |
VU 0357017 hydrochloride |
| Positive allosteric modulator of M1 receptors |
| 4437 |
VU 0357121 |
| Positive allosteric modulator of mGlu5 receptors |
| 4323 |
VU 0360172 hydrochloride |
| Positive allosteric modulator of mGlu5 receptors |
| 4394 |
VU 0360223 |
| Negative allosteric modulator of mGlu5 receptors |
| 3707 |
VU 0361737 |
| Selective positive allosteric modulator of mGlu4 receptors |
| 4371 |
VU 0364439 |
| Positive allosteric modulator of mGlu4 receptors |
| 4171 |
VU 0364739 hydrochloride |
| Potent and selective PLD2 inhibitor |
| 4469 |
VU 0364770 |
| Positive allosteric modulator of mGlu4 receptors |
| 4404 |
VU 0365114 |
| Positive allosteric modulator of M5 receptors |
| 5322 |
VU 0409106 |
| Potent and selective negative allosteric modulator of mGlu5 receptors |
| 5693 |
VU 0409551 |
| Selective positive allosteric modulator of mGlu5 receptors; brain penetrant and orally bioavailable |
| 5378 |
VU 0422288 |
| Selective positive allosteric modulator of group III mGlu receptors |
| 6895 |
VU 0424465 |
| Potent mGlu5 positive allosteric modulator and agonist; binds allosteric site with high affinity |
| 4719 |
VU 0463271 |
| Potent and selective KCC2 inhibitor |
| 6932 |
VU 0467485 |
| Potent and selective positive allosteric modulator of M4 receptors; orally bioavailable and brain penetrant |
| 5379 |
VU 0469650 hydrochloride |
| Potent and selective negative allosteric modulator of mGlu1 receptors |
| 6355 |
VU 0650991 |
| Non-competitive GLP-1 antagonist; orally bioavailable and brain penetrant |
| 3141 |
VU 10010 |
| Selective positive allosteric modulator of M4 receptors |
| 3383 |
VU 152100 |
| Positive allosteric modulator of M4 receptors |
| 3325 |
VU 1545 |
| Positive allosteric modulator of mGlu5 receptors |
| 4458 |
VU 29 |
| Potent positive allosteric modulator of mGlu5 receptors |
| 3891 |
VU 590 dihydrochloride |
| Inhibitor of Kir1.1 (ROMK) and Kir7.1 |
| 4197 |
VU 591 hydrochloride |
| Selective Kir1.1 (ROMK) inhibitor |
| 6928 |
VU 6001966 |
| Potent and selective negative allosteric modulator of mGlu2 receptors |
| 6893 |
VU 6005649 |
| Positive allosteric modulators of mGlu7 and mGlu8 receptors; also NK1 antagonist; brain penetrant |
| 4532 |
VUF 10166 |
| High affinity 5-HT3 antagonist |
| 4769 |
VUF 10460 |
| Selective H4 agonist |
| 4780 |
VUF 11207 fumarate |
| Potent ACKR3 (CXCR7) agonist |
| 5668 |
VUF 11222 |
| High affinity non-peptide CXCR3 agonist |
| 1359 |
VUF 5574 |
| Potent, selective hA3 antagonist |
| 2493 |
VUF 5681 dihydrobromide |
| Potent H3 receptor silent antagonist |
| 2494 |
VUF 8430 dihydrobromide |
| Potent and high affinity H4 agonist |
| 2988 |
VULM 1457 |
| ACAT inhibitor |
| 5907 |
VX 680 |
| High affinity and selective Aurora kinase inhibitor |
| 3915 |
VX 745 |
| Potent and selective p38α inhibitor |
| 7143 |
VX 765 New |
| High affinity and selective caspase-4 and caspase 1/ICE inhibitor; orally bioavailable |
| 6936 |
VZ 185 |
| Potent and selective BRD7/9 Degrader |
| 4206 |
Valdecoxib |
| Selective and potent COX-2 inhibitor |
| 3048 |
Valerenic acid |
| Positive allosteric modulator of GABAA receptors |
| 3373 |
Valinomycin |
| Selective K+ ionophore |
| 2815 |
Valproic acid, sodium salt |
| Histone deacetylase inhibitor |
| 4216 |
Valsartan |
| High affinity, selective AT1 antagonist |
| 5506 |
Vancomycin HCl |
| Antibiotic |
| 3754 |
Varenicline tartrate |
| Selective α4β2 nAChR partial agonist; orally active |
| 3377 |
(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin |
| Selective vasopressin V1A antagonist |
| 2935 |
[Arg8]-Vasopressin |
| Antidiuretic hormone |
| 2934 |
[Lys8]-Vasopressin |
| Antidiuretic hormone |
| 5680 |
Vatalanib succinate |
| Potent VEGFR inhibitor; also aromatase inhibitor |
| 7026 |
Veliparib dihydrochloride |
| High affinity PARP-1 and -2 inhibitor; orally bioavailable |
| 2917 |
Venlafaxine hydrochloride |
| 5-HT and NA reuptake inhibitor (SNRI) |
| 0654 |
Verapamil hydrochloride |
| CaV1.x blocker |
| 2918 |
Veratridine |
| Voltage-gated Na+ channel opener |
| 5305 |
Verteporfin |
| YAP inhibitor |
| 0653 |
(±)-Vesamicol hydrochloride |
| Inhibits ACh transport |
| 4988 |
Vialinin A |
| Inhibitor of USP4 and USP5/IsoT |
| 0808 |
Vigabatrin |
| GABA-T inhibitor |
| 6202 |
Vilazodone hydrochloride |
| Potent 5-HT1A partial agonist and SSRI; antidepressant |
| 1256 |
Vinblastine sulfate |
| Disrupts microtubules |
| 1257 |
Vincristine sulfate |
| Disrupts microtubules |
| 3401 |
Vinorelbine ditartrate |
| Selective mitotic microtubule antagonist |
| 0757 |
Vinpocetine |
| Na+ channel blocker |
| 3787 |
Viomycin |
| Antibiotic; inhibits bacterial DNA synthesis |
| 5395 |
Virodhamine trifluoroacetate |
| TFA salt of virodhamine, an endogenous cannabinoid receptor mixed agonist/antagonist |
| 4156 |
Vitamin D3 |
| Precursor of calcifediol (Cat. No. 4036). Naturally occurring form of vitamin D |
| 3596 |
Voglibose |
| Orally active α-glucosidase inhibitor |
| 3760 |
Voriconazole |
| Triazole antifungal agent |