Zolmitriptan |
A triptan that acts as an agonist of the serotonin (5-HT) receptors 5-HT1B… |
10 mg |
15871-10 |
More Info
|
Zolmitriptan |
A triptan that acts as an agonist of the serotonin (5-HT) receptors 5-HT1B… |
25 mg |
15871-25 |
More Info
|
Zolmitriptan |
A triptan that acts as an agonist of the serotonin (5-HT) receptors 5-HT1B… |
5 mg |
15871-5 |
More Info
|
Zolmitriptan |
A triptan that acts as an agonist of the serotonin (5-HT) receptors 5-HT1B… |
50 mg |
15871-50 |
More Info
|
Zoniporide (hydrochloride) |
Selectively inhibits human NHE-1 with an IC50 value of 14 nM; reduces infa… |
1 mg |
16004-1 |
More Info
|
Zoniporide (hydrochloride) |
Selectively inhibits human NHE-1 with an IC50 value of 14 nM; reduces infa… |
10 mg |
16004-10 |
More Info
|
Zoniporide (hydrochloride) |
Selectively inhibits human NHE-1 with an IC50 value of 14 nM; reduces infa… |
5 mg |
16004-5 |
More Info
|
Zoniporide (hydrochloride) |
Selectively inhibits human NHE-1 with an IC50 value of 14 nM; reduces infa… |
50 mg |
16004-50 |
More Info
|
Zonisamide |
A broad-spectrum sulfonamide antiepileptic agent; blocks repeated firing o… |
1 g |
24183-1 |
More Info
|
Zonisamide |
A broad-spectrum sulfonamide antiepileptic agent; blocks repeated firing o… |
100 mg |
24183-100 |
More Info
|
Zonisamide |
A broad-spectrum sulfonamide antiepileptic agent; blocks repeated firing o… |
250 mg |
24183-250 |
More Info
|
Zonisamide |
A broad-spectrum sulfonamide antiepileptic agent; blocks repeated firing o… |
500 mg |
24183-500 |
More Info
|
Zonisamide-13C2,15N |
An internal standard for the quantification of zonisamide by GC- or LC-MS |
1 mg |
28807-1 |
More Info
|
Zopolrestat |
A potent aldose reductase inhibitor (IC50s = 1.9 and 41 nM for the human p… |
1 mg |
29185-1 |
More Info
|
Zopolrestat |
A potent aldose reductase inhibitor (IC50s = 1.9 and 41 nM for the human p… |
10 mg |
29185-10 |
More Info
|
Zopolrestat |
A potent aldose reductase inhibitor (IC50s = 1.9 and 41 nM for the human p… |
5 mg |
29185-5 |
More Info
|
Zosuquidar (hydrochloride) |
A modulator of P-gp (Ki = 59 nM); restores the sensitivity of P-gp-express… |
1 mg |
21533-1 |
More Info
|
Zosuquidar (hydrochloride) |
A modulator of P-gp (Ki = 59 nM); restores the sensitivity of P-gp-express… |
10 mg |
21533-10 |
More Info
|
Zosuquidar (hydrochloride) |
A modulator of P-gp (Ki = 59 nM); restores the sensitivity of P-gp-express… |
25 mg |
21533-25 |
More Info
|
Zosuquidar (hydrochloride) |
A modulator of P-gp (Ki = 59 nM); restores the sensitivity of P-gp-express… |
5 mg |
21533-5 |
More Info
|
Zotarolimus |
A macrocyclic lactone immunosuppressant; binds to FKBP12 (IC50 = 2.57 nM);… |
1 mg |
29246-1 |
More Info
|
Zotarolimus |
A macrocyclic lactone immunosuppressant; binds to FKBP12 (IC50 = 2.57 nM);… |
10 mg |
29246-10 |
More Info
|
Zotarolimus |
A macrocyclic lactone immunosuppressant; binds to FKBP12 (IC50 = 2.57 nM);… |
25 mg |
29246-25 |
More Info
|
Zotarolimus |
A macrocyclic lactone immunosuppressant; binds to FKBP12 (IC50 = 2.57 nM);… |
5 mg |
29246-5 |
More Info
|
Zotepine |
An atypical antipsychotic; a dopamine D2 and D3 receptor antagonist (Kis =… |
10 mg |
23909-10 |
More Info
|
Zotepine |
An atypical antipsychotic; a dopamine D2 and D3 receptor antagonist (Kis =… |
100 mg |
23909-100 |
More Info
|
Zotepine |
An atypical antipsychotic; a dopamine D2 and D3 receptor antagonist (Kis =… |
25 mg |
23909-25 |
More Info
|
Zotepine |
An atypical antipsychotic; a dopamine D2 and D3 receptor antagonist (Kis =… |
50 mg |
23909-50 |
More Info
|
Zoxazolamine |
A potent skeletal muscle relaxant that also has uricosuric activity; recov… |
1 g |
17565-1 |
More Info
|
Zoxazolamine |
A potent skeletal muscle relaxant that also has uricosuric activity; recov… |
10 g |
17565-10 |
More Info
|
Zoxazolamine |
A potent skeletal muscle relaxant that also has uricosuric activity; recov… |
25 g |
17565-25 |
More Info
|
Zoxazolamine |
A potent skeletal muscle relaxant that also has uricosuric activity; recov… |
5 g |
17565-5 |
More Info
|
(5Z)-7-Oxozeaenol |
A TAK1 inhibitor (IC50 = 8.1 nM in the presence of TAB1); selective for TA… |
1 mg |
17459-1 |
More Info
|
(5Z)-7-Oxozeaenol |
A TAK1 inhibitor (IC50 = 8.1 nM in the presence of TAB1); selective for TA… |
5 mg |
17459-5 |
More Info
|
7(Z)-Pentacosene |
An unsaturated cuticular hydrocarbon that acts as a contact sex pheromone… |
1 mg |
9000530-1 |
More Info
|
7(Z)-Pentacosene |
An unsaturated cuticular hydrocarbon that acts as a contact sex pheromone… |
10 mg |
9000530-10 |
More Info
|
7(Z)-Pentacosene |
An unsaturated cuticular hydrocarbon that acts as a contact sex pheromone… |
5 mg |
9000530-5 |
More Info
|
7(Z)-Pentacosene |
An unsaturated cuticular hydrocarbon that acts as a contact sex pheromone… |
50 mg |
9000530-50 |
More Info
|
9(Z)-Pentacosene |
A cuticular hydrocarbon and insect sex hormone; found in the cuticle of fe… |
1 mg |
9002807-1 |
More Info
|
9(Z)-Pentacosene |
A cuticular hydrocarbon and insect sex hormone; found in the cuticle of fe… |
10 mg |
9002807-10 |
More Info
|
9(Z)-Pentacosene |
A cuticular hydrocarbon and insect sex hormone; found in the cuticle of fe… |
5 mg |
9002807-5 |
More Info
|
9(Z)-Pentacosene |
A cuticular hydrocarbon and insect sex hormone; found in the cuticle of fe… |
50 mg |
9002807-50 |
More Info
|
10(Z)-Pentadecenoic Acid |
A 15-carbon monounsaturated fatty acid; inhibits IFN-γ-induced produ… |
1 mg |
22362-1 |
More Info
|
10(Z)-Pentadecenoic Acid |
A 15-carbon monounsaturated fatty acid; inhibits IFN-γ-induced produ… |
10 mg |
22362-10 |
More Info
|
10(Z)-Pentadecenoic Acid |
A 15-carbon monounsaturated fatty acid; inhibits IFN-γ-induced produ… |
25 mg |
22362-25 |
More Info
|
10(Z)-Pentadecenoic Acid |
A 15-carbon monounsaturated fatty acid; inhibits IFN-γ-induced produ… |
5 mg |
22362-5 |
More Info
|
10(Z)-Pentadecenoic Acid methyl ester |
A methyl ester form of 10(Z)-pentadecenoic acid; has been used as a standa… |
50 mg |
26729-50 |
More Info
|
Z-Phe-Tyr(tBu)-diazomethylketone |
An inhibitor of cathepsin L (Kinact = 200,000 M-1s-1); selective for cathe… |
1 mg |
27877-1 |
More Info
|
Z-Phe-Tyr(tBu)-diazomethylketone |
An inhibitor of cathepsin L (Kinact = 200,000 M-1s-1); selective for cathe… |
10 mg |
27877-10 |
More Info
|
Z-Phe-Tyr(tBu)-diazomethylketone |
An inhibitor of cathepsin L (Kinact = 200,000 M-1s-1); selective for cathe… |
25 mg |
27877-25 |
More Info
|
Z-Phe-Tyr(tBu)-diazomethylketone |
An inhibitor of cathepsin L (Kinact = 200,000 M-1s-1); selective for cathe… |
5 mg |
27877-5 |
More Info
|
(Z)-PUGNAc |
An analog of GlcNAc that reversibly inhibits NCOAT (O-GlcNAcase) |
1 mg |
17151-1 |
More Info
|
(Z)-PUGNAc |
An analog of GlcNAc that reversibly inhibits NCOAT (O-GlcNAcase) |
10 mg |
17151-10 |
More Info
|
(Z)-PUGNAc |
An analog of GlcNAc that reversibly inhibits NCOAT (O-GlcNAcase) |
5 mg |
17151-5 |
More Info
|
ZSTK474 |
A selective inhibitor of class I PI3K isoforms (IC50s = 17, 53, and 6 nM f… |
10 mg |
17381-10 |
More Info
|
ZSTK474 |
A selective inhibitor of class I PI3K isoforms (IC50s = 17, 53, and 6 nM f… |
25 mg |
17381-25 |
More Info
|
ZSTK474 |
A selective inhibitor of class I PI3K isoforms (IC50s = 17, 53, and 6 nM f… |
5 mg |
17381-5 |
More Info
|
ZSTK474 |
A selective inhibitor of class I PI3K isoforms (IC50s = 17, 53, and 6 nM f… |
50 mg |
17381-50 |
More Info
|
7(Z)-Tricosene |
An unsaturated cuticular hydrocarbon that acts as a pheromone in some inse… |
1 mg |
9000313-1 |
More Info
|
7(Z)-Tricosene |
An unsaturated cuticular hydrocarbon that acts as a pheromone in some inse… |
10 mg |
9000313-10 |
More Info
|
7(Z)-Tricosene |
An unsaturated cuticular hydrocarbon that acts as a pheromone in some inse… |
5 mg |
9000313-5 |
More Info
|
7(Z)-Tricosene |
An unsaturated cuticular hydrocarbon that acts as a pheromone in some inse… |
50 mg |
9000313-50 |
More Info
|
9(Z)-Tricosene |
An insect pheromone used in pesticides; activates antennal basiconic Or7a… |
1 g |
13236-1 |
More Info
|
9(Z)-Tricosene |
An insect pheromone used in pesticides; activates antennal basiconic Or7a… |
5 g |
13236-5 |
More Info
|
9(Z)-Tricosene |
An insect pheromone used in pesticides; activates antennal basiconic Or7a… |
500 mg |
13236-500 |
More Info
|
Zuclopenthixol |
A dopamine receptor antagonist (Kis = 9.8 and 1.5 nM for D1 and D2 recepto… |
100 mg |
24961-100 |
More Info
|
Zuclopenthixol |
A dopamine receptor antagonist (Kis = 9.8 and 1.5 nM for D1 and D2 recepto… |
250 mg |
24961-250 |
More Info
|
Zuclopenthixol |
A dopamine receptor antagonist (Kis = 9.8 and 1.5 nM for D1 and D2 recepto… |
500 mg |
24961-500 |
More Info
|
Z-VAD-AMC (acetate) |
A caspase-1 fluorogenic substrate; upon enzymatic cleavage, AMC is release… |
1 mg |
27142-1 |
More Info
|
Z-VAD-AMC (acetate) |
A caspase-1 fluorogenic substrate; upon enzymatic cleavage, AMC is release… |
5 mg |
27142-5 |
More Info
|
Z-VAD-AMC (acetate) |
A caspase-1 fluorogenic substrate; upon enzymatic cleavage, AMC is release… |
500 µg |
27142-500 |
More Info
|
Z-VA-DL-D(OMe)-FMK (trifluoroacetate salt) |
A pan-caspase inhibitor; inhibits anti-Fas antibody-induced cleavage of ca… |
1 mg |
27421-1 |
More Info
|
Z-VA-DL-D(OMe)-FMK (trifluoroacetate salt) |
A pan-caspase inhibitor; inhibits anti-Fas antibody-induced cleavage of ca… |
500 µg |
27421-500 |
More Info
|
Z-VAD(OH)-FMK |
An irreversible tripeptide inhibitor of all caspases; useful in studies in… |
1 mg |
14467-1 |
More Info
|
Z-VAD(OH)-FMK |
An irreversible tripeptide inhibitor of all caspases; useful in studies in… |
5 mg |
14467-5 |
More Info
|