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 |