(−)-Nutlin-3 |
An inhibitor of the p53-Mdm2 interaction (IC50 = 0.09 µM); increases… |
1 mg |
18585-1 |
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(−)-Nutlin-3 |
An inhibitor of the p53-Mdm2 interaction (IC50 = 0.09 µM); increases… |
10 mg |
18585-10 |
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(−)-Nutlin-3 |
An inhibitor of the p53-Mdm2 interaction (IC50 = 0.09 µM); increases… |
25 mg |
18585-25 |
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|
(−)-Nutlin-3 |
An inhibitor of the p53-Mdm2 interaction (IC50 = 0.09 µM); increases… |
5 mg |
18585-5 |
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(−)-Pentazocine |
An analytical reference standard categorized as an opioid; has analgesic p… |
1 mg |
15912-1 |
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(−)-Pentazocine |
An analytical reference standard categorized as an opioid; has analgesic p… |
5 mg |
15912-5 |
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(−)-Perillyl Alcohol |
A monoterpene alcohol with diverse biological activities; reduces producti… |
10 g |
21860-10 |
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(−)-Perillyl Alcohol |
A monoterpene alcohol with diverse biological activities; reduces producti… |
25 g |
21860-25 |
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(−)-Perillyl Alcohol |
A monoterpene alcohol with diverse biological activities; reduces producti… |
5 g |
21860-5 |
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(−)-Physostigmine (salicylate) |
An alkaloid and cholinergic agent; inhibits AChE (IC50 = 0.67 nM); inhibit… |
100 mg |
33106-100 |
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(−)-Physostigmine (salicylate) |
An alkaloid and cholinergic agent; inhibits AChE (IC50 = 0.67 nM); inhibit… |
25 mg |
33106-25 |
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(−)-Physostigmine (salicylate) |
An alkaloid and cholinergic agent; inhibits AChE (IC50 = 0.67 nM); inhibit… |
250 mg |
33106-250 |
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(−)-Physostigmine (salicylate) |
An alkaloid and cholinergic agent; inhibits AChE (IC50 = 0.67 nM); inhibit… |
50 mg |
33106-50 |
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(−)-Pinoresinol |
A lignan with diverse biological activities; scavenges DPPH and ABTS radic… |
1 mg |
36850-1 |
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(−)-Pinoresinol |
A lignan with diverse biological activities; scavenges DPPH and ABTS radic… |
10 mg |
36850-10 |
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(−)-Pinoresinol |
A lignan with diverse biological activities; scavenges DPPH and ABTS radic… |
5 mg |
36850-5 |
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(−)-Propoxyphene (hydrochloride) |
An analytical reference standard categorized as an opioid; intended for re… |
1 mg |
22769-1 |
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(−)-Propoxyphene (hydrochloride) |
An analytical reference standard categorized as an opioid; intended for re… |
5 mg |
22769-5 |
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(−)-Rolipram |
A PDE4 inhibitor (IC50 = 0.22 µM for the guinea pig eosinophil enzym… |
1 mg |
31111-1 |
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(−)-Rolipram |
A PDE4 inhibitor (IC50 = 0.22 µM for the guinea pig eosinophil enzym… |
10 mg |
31111-10 |
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(−)-Rolipram |
A PDE4 inhibitor (IC50 = 0.22 µM for the guinea pig eosinophil enzym… |
5 mg |
31111-5 |
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(−)-Rugulosin |
A fungal metabolite; 3-10-fold more cytotoxic to HeLa and L cells compared… |
1 mg |
25477-1 |
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(−)-Rugulosin |
A fungal metabolite; 3-10-fold more cytotoxic to HeLa and L cells compared… |
5 mg |
25477-5 |
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(−)-(S)-Cathinone (hydrochloride) |
The main psychoactive alkaloid from the khat plant and a naturally occurri… |
10 mg |
13869-10 |
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(−)-(S)-Cathinone (hydrochloride) |
The main psychoactive alkaloid from the khat plant and a naturally occurri… |
5 mg |
13869-5 |
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(−)-(S)-Cathinone (hydrochloride) (exempt preparation) |
The main psychoactive alkaloid from the khat plant and a naturally occurri… |
1 mg |
15655-1 |
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(−)-Sweroside |
An iridoid glycoside; inhibits LPS-induced production of PGE2 and ROS in m… |
10 mg |
33454-10 |
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(−)-Sweroside |
An iridoid glycoside; inhibits LPS-induced production of PGE2 and ROS in m… |
25 mg |
33454-25 |
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(−)-Sweroside |
An iridoid glycoside; inhibits LPS-induced production of PGE2 and ROS in m… |
5 mg |
33454-5 |
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(−)-Sweroside |
An iridoid glycoside; inhibits LPS-induced production of PGE2 and ROS in m… |
50 mg |
33454-50 |
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(−)-Syringaresinol di-O-glucoside |
A phenolic glucoside with in vitro neuroprotective activity; reduces gluta… |
1 mg |
36672-1 |
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(−)-Syringaresinol di-O-glucoside |
A phenolic glucoside with in vitro neuroprotective activity; reduces gluta… |
10 mg |
36672-10 |
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(−)-Syringaresinol di-O-glucoside |
A phenolic glucoside with in vitro neuroprotective activity; reduces gluta… |
25 mg |
36672-25 |
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(−)-Syringaresinol di-O-glucoside |
A phenolic glucoside with in vitro neuroprotective activity; reduces gluta… |
5 mg |
36672-5 |
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(−)-Terpinen-4-ol |
A monoterpene alcohol with arrhythmogenic and anticonvulsant activities; i… |
1 g |
38964-1 |
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(−)-Terpinen-4-ol |
A monoterpene alcohol with arrhythmogenic and anticonvulsant activities; i… |
5 g |
38964-5 |
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(−)-Terpinen-4-ol |
A monoterpene alcohol with arrhythmogenic and anticonvulsant activities; i… |
500 mg |
38964-500 |
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(−)-trans-C75 |
An enantiomer of C75, which in racemic form is a stable FASN inhibitor tha… |
1 mg |
9000784-1 |
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(−)-trans-C75 |
An enantiomer of C75, which in racemic form is a stable FASN inhibitor tha… |
5 mg |
9000784-5 |
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(−)-Triptonide |
A diterpenoid with diverse biological activities; inhibits IL-2 production… |
1 mg |
29156-1 |
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(−)-Triptonide |
A diterpenoid with diverse biological activities; inhibits IL-2 production… |
10 mg |
29156-10 |
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(−)-Triptonide |
A diterpenoid with diverse biological activities; inhibits IL-2 production… |
50 mg |
29156-50 |
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(−)-Viriditoxin |
A mycotoxin; active against MSSA and MRSA, tetracycline-sensitive and -res… |
500 µg |
26601-500 |
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(−)-Voacangarine |
A cytotoxic indole alkaloid; cytotoxic to HepG2, A375, MDA-MB-231, SH-SY5Y… |
1 mg |
25468-1 |
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(−)-Voacangarine |
A cytotoxic indole alkaloid; cytotoxic to HepG2, A375, MDA-MB-231, SH-SY5Y… |
10 mg |
25468-10 |
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(−)-Voacangarine |
A cytotoxic indole alkaloid; cytotoxic to HepG2, A375, MDA-MB-231, SH-SY5Y… |
5 mg |
25468-5 |
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m-Iodobenzylguanidine (hemisulfate) |
A norepinephrine analogue with anticancer activity; inhibits cell growth i… |
1 mg |
19998-1 |
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m-Iodobenzylguanidine (hemisulfate) |
A norepinephrine analogue with anticancer activity; inhibits cell growth i… |
10 mg |
19998-10 |
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m-Iodobenzylguanidine (hemisulfate) |
A norepinephrine analogue with anticancer activity; inhibits cell growth i… |
5 mg |
19998-5 |
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MIPS521 |
An adenosine A1 receptor positive allosteric modulator; binds to adenosine… |
10 mg |
37776-10 |
More Info
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