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Cat No. Product Name
T12597 5-HT2 antagonist 1 5-HT2 antagonist 1 is a potent 5-HT2 receptor antagonist, has weak α1 adrenoceptor blocking activity.
T19536 Pyruvic aldehyde Pyruvic aldehyde is a flavoring agent, and in tanning.
T12598 Pz-1 Pz-1 is a potent inhibitor of RET and VEGFR2 (IC50s <1 for both wild type kinases).
T12599 QM31 QM31 is a selective Apaf-1 inhibitor(inbitita formation of the apoptosome with IC50 of 7.9μM).
T12600 QM385 QM385 is a potent inhibitor of sepiapterin reductase (SPR)(IC50 of 1.49 nM).
T12601 QPX7728 bis-acetoxy methyl ester QPX7728 bis-acetoxy methyl ester is an inhibitor of boronic acid β-lactamase.
T12602 QPX7728 methoxy acetoxy methy ester QPX7728 methoxy acetoxy methy ester is an inhibitor of boronic acid β-lactamase.
T12603 QPX7728-OH disodium QPX7728-OH disodium is an inhibitor of boronic acid β-lactamase.
T12604 QPX7728 QPX7728 is an of ultra-broad-spectrum boronic acid beta-lactamase.
T12618 Quetiapine D4 fumarate Quetiapine D4 fumarate is the deuterium labeled Quetiapine fumarate. Quetiapine fumarate is a agonist of 5-HT receptors and a antagonist of dopamine receptor,wi...
T12618L Quetiapine D4 hemifumarate Quetiapine D4 hemifumarate is the deuterium labeled Quetiapine hemifumarate. Quetiapine hemifumarate is a agonist of 5-HT receptors and a antagonist of dopamine...
T12619 Quetiapine sulfoxide Quetiapine sulfoxide is a main Quetiapinem metabolite. Quetiapine is a agonist of 5-HT receptors and a antagonist of dopamine receptor.Quetiapine is a second-ge...
T12619L Quetiapine sulfoxide dihydrochloride Quetiapine sulfoxide dihydrochloride is a main Quetiapinem metabolite. Quetiapine is a agonist of 5-HT receptors and a antagonist of dopamine receptor.Quetiapin...
T12619L2 Quetiapine sulfoxide hydrochloride Quetiapine sulfoxide hydrochloride is a main metabolite of Quetiapinem. Quetiapine is a 5-HT receptors agonist and a dopamine receptor antagonist.
T12605 Quinagolide hydrochloride Quinagolide hydrochloride is a selective agonist of dopamine D2 receptor.
T13854 Quininic acid Quininic acid is a natural product purified from Eucalyptus globulus, cinchona bark, and other plant products, is the most abundant organic acid.
T13855 Quinotolast sodium Quinotolast sodium inhibits histamine, LTC4 and PGD2 release in a concentration-dependent manner in the concentration range of 1-100 μg/mL.
T12607 Quinupristin Quinupristin is a streptogramin antibiotic.
T19537 Quizalofop-p-ethyl Quizalofop-P-ethyl is a selective,slightly toxic, postemergence phenoxy herbicide.
T19538 (R)-(-)-1,3-Butanediol (R)-(-)-1,3-Butanediol is used for regulate the metabolism of carbohydrate and lipid.
T12610 (R)-3-Hydroxy Midostaurin (R)-3-Hydroxy Midostaurin is a potent inhibitor of kinases,is a major metabolite of midostaurin undergoing by the hepatic CYP3A4 enzyme,has the potential for ac...
T12611 R 80123 R 80123 is a highly selective inhibitor of phosphodiesterase,is the Z-isomer of R 79595
T12612 (R)-Apremilast (R)-Apremilast ((R)-CC-10004) is a enantiomer of Apremilast.
T12613 (R)-BAY-85-8501 (R)-BAY-85-8501 is the less active enantiomer of BAY-85-8501. BAY-85-8501 is a selective and potent Human Neutrophil Elastase (HNE)inhibitor(IC50 of 65 pM).
T12615 (R)-Carvedilol (R)-Carvedilol is a non-selective blocker of β/α-1. (R)-Carvedilol exerts protection against the vascular or cardiac toxicity of Doxorubicin (DOX).
T12616 (R)-CE3F4 (R)-CE3F4 is a selective inhibitor of exchange protein directly activated by cAMP isoform 1 (Epac1)(IC50 of 4.2 μM),
T12620 (R)-CSN5i-3 (R)-CSN5i-3 is the (R)-enantiomer of CSN5i-3. CSN5i-3 is a potent, selective and orally available CSN5 inhibitor.
T13856 (R)-DNMDP (R)-DNMDP is a potent and selective agent of cancer cell cytotoxic.
T12621 (R)-FT671 (R)-FT671 is the R-isomer of FT671. FT671 is a potent, non-covalent and selective inhibitor of USP7 (IC50 of 52 nM)
T12622 (R)-Hydroxychloroquine (R)-Hydroxychloroquine is the enantiomer of Hydroxychloroquine. Hydroxychloroquine is an agent of synthetic antimalarial.
T12623 (R)-JNJ-31020028 (R)-JNJ-31020028 is a high affinity, selective brain penetrant antagonist of neuropeptide Y Y2 receptor(pIC50 values of 8.07, 8.22 and 8.21 for human, rat, and ...
T12624 (R)-Ketorolac (R)-Ketorolac is the R-enantiomer of Ketorolac, with potent analgesic activity.
T19539 (R)-Leucic acid (R)-Leucic acid is an metabolite of amino acid.
T12627 (R)-​Linezolid (R)-Linezolid is an impurity of Linezolid . Linezolid acts by inhibiting the initiation of bacterial protein synthesis.
T12629 (R)-MIK665 (R)-MIK665 is the less active enantiomer of MIK665. MIK665 is a special inhibitor of Mcl-1(IC50 of 1.81 nM).
T12633 (R)-Nicardipine (R)-Nicardipine is the less active R enantiomer of Nicardipine. Nicardipine is a blocker of calcium channel(IC50 of 1 μM for blocking cardiac calcium channels)...
T12634 (R)-NVS-ZP7-4 (R)-NVS-ZP7-4 is the R-isomer of NVS-ZP7-4. NVS-ZP7-4 is a inhibitor of Zinc transporter SLC39A7 .
T12635 (R)-Plevitrexed (R)-Plevitrexed is a less active enantiomer of Plevitrexed. Plevitrexed is an orally active and potent inhibitor of thymidylate synthase (TS).
T12636 (R)-(+)-Anatabine (R)-(+)-Anatabine is an less active R-enantiomer of Anatabine. Anatabine is a potent agonist of α4β2 nAChR.
T12637 (R)-(+)-HA-966 (R)-(+)-HA-966 ((+)-HA-966) is a partial agonist/antagonist of glycine site of the N-methyl-D-aspartate (NMDA) receptor complex. (R)-(+)-HA-966 selectively bloc...
T12639 (R)-PS210 (R)-PS210, the R enantiomer of PS210 is a substrate-selective allosteric PDK1 activator with an (AC50 of 1.8 μM).
T12640 (R,R)-Glycopyrrolate (R,R)-Glycopyrrolate is an agent of anticholinergic, has the ability to reduce the frequency of drooling in vivo with developmental disabilities.
T19540 (R,R)-(+)-Hydrobenzoin (R,R)-(+)-Hydrobenzoin is a organocatalysts.
T13857 (R,S)-Anatabine (R,S)-Anatabine is a minor tobacco alkaloid found in the Solanaceae family of plants,and can be used as a specific marker for the detection of tobacco use.
T12641 (R)-SCH 42495 (R)-SCH 42495 is the less active enantiomer of SCH 42495. SCH 42495 is an orally active inhibitor of neutral metalloendopeptidase (NEP), with antihypertensive e...
T12642 (R)-Simurosertib (R)-Simurosertib is the (R)-enantiomer of Simurosertib. Simurosertib is an orally active, selective and ATP-competitive cell division inhibitor of cycle 7 (CDC7...
T12644 (R)-Thalidomide (R)-Thalidomide is the R-enantiomer of Thalidomide, has sedative properties.
T12645 (R)-Trolox (R)-Trolox is a water soluble vitamin E analogue and a competitive tyrosinase inhibitor (Ki value of 0.83 mM and a ID50 value of 1.88 mM).
T12646 (R)-Verapamil hydrochloride (R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is a inhibitor of P-Glycoprotein.
T12647 (R)-VU 6008667 (R)-VU 6008667 is devoid of M5 NAM activity (IC50>10 μM).
5-HT2 antagonist 1
T12597CAS 191592-09-3
5-HT2 antagonist 1 is a potent 5-HT2 receptor antagonist, has weak α1 adrenoceptor blocking activity.
Pyruvic aldehyde
T19536CAS 78-98-8
Pyruvic aldehyde is a flavoring agent, and in tanning.
Pz-1
T12598CAS 1800505-64-9
Pz-1 is a potent inhibitor of RET and VEGFR2 (IC50s <1 for both wild type kinases).
QM31
T12599CAS 937735-00-7
QM31 is a selective Apaf-1 inhibitor(inbitita formation of the apoptosome with IC50 of 7.9μM).
QM385
T12600CAS 2093421-02-2
QM385 is a potent inhibitor of sepiapterin reductase (SPR)(IC50 of 1.49 nM).
QPX7728 bis-acetoxy methyl ester
T12601CAS 2170834-56-5
QPX7728 bis-acetoxy methyl ester is an inhibitor of boronic acid β-lactamase.
QPX7728 methoxy acetoxy methy ester
T12602CAS 2170834-57-6
QPX7728 methoxy acetoxy methy ester is an inhibitor of boronic acid β-lactamase.
QPX7728-OH disodium
T12603CAS 2170848-99-2
QPX7728-OH disodium is an inhibitor of boronic acid β-lactamase.
QPX7728
T12604CAS 2170834-63-4
QPX7728 is an of ultra-broad-spectrum boronic acid beta-lactamase.
Quetiapine D4 fumarate
T12618CAS 1287376-15-1
Quetiapine D4 fumarate is the deuterium labeled Quetiapine fumarate. Quetiapine fumarate is a agonist of 5-HT receptors and a antagonist of dopamine receptor,wi...
Quetiapine D4 hemifumarate
T12618LCAS 1217310-65-0
Quetiapine D4 hemifumarate is the deuterium labeled Quetiapine hemifumarate. Quetiapine hemifumarate is a agonist of 5-HT receptors and a antagonist of dopamine...
Quetiapine sulfoxide
T12619CAS 329216-63-9
Quetiapine sulfoxide is a main Quetiapinem metabolite. Quetiapine is a agonist of 5-HT receptors and a antagonist of dopamine receptor.Quetiapine is a second-ge...
Quetiapine sulfoxide dihydrochloride
T12619LCAS 329218-11-3
Quetiapine sulfoxide dihydrochloride is a main Quetiapinem metabolite. Quetiapine is a agonist of 5-HT receptors and a antagonist of dopamine receptor.Quetiapin...
Quetiapine sulfoxide hydrochloride
T12619L2CAS
Quetiapine sulfoxide hydrochloride is a main metabolite of Quetiapinem. Quetiapine is a 5-HT receptors agonist and a dopamine receptor antagonist.
Quinagolide hydrochloride
T12605CAS 94424-50-7
Quinagolide hydrochloride is a selective agonist of dopamine D2 receptor.
Quininic acid
T13854CAS 86-68-0
Quininic acid is a natural product purified from Eucalyptus globulus, cinchona bark, and other plant products, is the most abundant organic acid.
Quinotolast sodium
T13855CAS 101193-62-8
Quinotolast sodium inhibits histamine, LTC4 and PGD2 release in a concentration-dependent manner in the concentration range of 1-100 μg/mL.
Quinupristin
T12607CAS 120138-50-3
Quinupristin is a streptogramin antibiotic.
Quizalofop-p-ethyl
T19537CAS 100646-51-3
Quizalofop-P-ethyl is a selective,slightly toxic, postemergence phenoxy herbicide.
(R)-(-)-1,3-Butanediol
T19538CAS 6290-03-5
(R)-(-)-1,3-Butanediol is used for regulate the metabolism of carbohydrate and lipid.
(R)-3-Hydroxy Midostaurin
T12610CAS 155848-20-7
(R)-3-Hydroxy Midostaurin is a potent inhibitor of kinases,is a major metabolite of midostaurin undergoing by the hepatic CYP3A4 enzyme,has the potential for ac...
R 80123
T12611CAS 133718-30-6
R 80123 is a highly selective inhibitor of phosphodiesterase,is the Z-isomer of R 79595
(R)-Apremilast
T12612CAS 608141-44-2
(R)-Apremilast ((R)-CC-10004) is a enantiomer of Apremilast.
(R)-BAY-85-8501
T12613CAS
(R)-BAY-85-8501 is the less active enantiomer of BAY-85-8501. BAY-85-8501 is a selective and potent Human Neutrophil Elastase (HNE)inhibitor(IC50 of 65 pM).
(R)-Carvedilol
T12615CAS 95093-99-5
(R)-Carvedilol is a non-selective blocker of β/α-1. (R)-Carvedilol exerts protection against the vascular or cardiac toxicity of Doxorubicin (DOX).
(R)-CE3F4
T12616CAS 1593478-56-8
(R)-CE3F4 is a selective inhibitor of exchange protein directly activated by cAMP isoform 1 (Epac1)(IC50 of 4.2 μM),
(R)-CSN5i-3
T12620CAS
(R)-CSN5i-3 is the (R)-enantiomer of CSN5i-3. CSN5i-3 is a potent, selective and orally available CSN5 inhibitor.
(R)-DNMDP
T13856CAS 1630760-60-9
(R)-DNMDP is a potent and selective agent of cancer cell cytotoxic.
(R)-FT671
T12621CAS 1959551-27-9
(R)-FT671 is the R-isomer of FT671. FT671 is a potent, non-covalent and selective inhibitor of USP7 (IC50 of 52 nM)
(R)-Hydroxychloroquine
T12622CAS 137433-23-9
(R)-Hydroxychloroquine is the enantiomer of Hydroxychloroquine. Hydroxychloroquine is an agent of synthetic antimalarial.
(R)-JNJ-31020028
T12623CAS 1094873-17-2
(R)-JNJ-31020028 is a high affinity, selective brain penetrant antagonist of neuropeptide Y Y2 receptor(pIC50 values of 8.07, 8.22 and 8.21 for human, rat, and ...
(R)-Ketorolac
T12624CAS 66635-93-6
(R)-Ketorolac is the R-enantiomer of Ketorolac, with potent analgesic activity.
(R)-Leucic acid
T19539CAS 20312-37-2
(R)-Leucic acid is an metabolite of amino acid.
(R)-​Linezolid
T12627CAS 872992-20-6
(R)-Linezolid is an impurity of Linezolid . Linezolid acts by inhibiting the initiation of bacterial protein synthesis.
(R)-MIK665
T12629CAS 1799831-02-9
(R)-MIK665 is the less active enantiomer of MIK665. MIK665 is a special inhibitor of Mcl-1(IC50 of 1.81 nM).
(R)-Nicardipine
T12633CAS 76093-35-1
(R)-Nicardipine is the less active R enantiomer of Nicardipine. Nicardipine is a blocker of calcium channel(IC50 of 1 μM for blocking cardiac calcium channels)...
(R)-NVS-ZP7-4
T12634CAS
(R)-NVS-ZP7-4 is the R-isomer of NVS-ZP7-4. NVS-ZP7-4 is a inhibitor of Zinc transporter SLC39A7 .
(R)-Plevitrexed
T12635CAS 153537-74-7
(R)-Plevitrexed is a less active enantiomer of Plevitrexed. Plevitrexed is an orally active and potent inhibitor of thymidylate synthase (TS).
(R)-(+)-Anatabine
T12636CAS 126454-22-6
(R)-(+)-Anatabine is an less active R-enantiomer of Anatabine. Anatabine is a potent agonist of α4β2 nAChR.
(R)-(+)-HA-966
T12637CAS 123931-04-4
(R)-(+)-HA-966 ((+)-HA-966) is a partial agonist/antagonist of glycine site of the N-methyl-D-aspartate (NMDA) receptor complex. (R)-(+)-HA-966 selectively bloc...
(R)-PS210
T12639CAS 1410101-89-1
(R)-PS210, the R enantiomer of PS210 is a substrate-selective allosteric PDK1 activator with an (AC50 of 1.8 μM).
(R,R)-Glycopyrrolate
T12640CAS 475468-09-8
(R,R)-Glycopyrrolate is an agent of anticholinergic, has the ability to reduce the frequency of drooling in vivo with developmental disabilities.
(R,R)-(+)-Hydrobenzoin
T19540CAS 52340-78-0
(R,R)-(+)-Hydrobenzoin is a organocatalysts.
(R,S)-Anatabine
T13857CAS 2743-90-0
(R,S)-Anatabine is a minor tobacco alkaloid found in the Solanaceae family of plants,and can be used as a specific marker for the detection of tobacco use.
(R)-SCH 42495
T12641CAS 156792-25-5
(R)-SCH 42495 is the less active enantiomer of SCH 42495. SCH 42495 is an orally active inhibitor of neutral metalloendopeptidase (NEP), with antihypertensive e...
(R)-Simurosertib
T12642CAS 1330782-69-8
(R)-Simurosertib is the (R)-enantiomer of Simurosertib. Simurosertib is an orally active, selective and ATP-competitive cell division inhibitor of cycle 7 (CDC7...
(R)-Thalidomide
T12644CAS 2614-06-4
(R)-Thalidomide is the R-enantiomer of Thalidomide, has sedative properties.
(R)-Trolox
T12645CAS 53101-49-8
(R)-Trolox is a water soluble vitamin E analogue and a competitive tyrosinase inhibitor (Ki value of 0.83 mM and a ID50 value of 1.88 mM).
(R)-Verapamil hydrochloride
T12646CAS 38176-02-2
(R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is a inhibitor of P-Glycoprotein.
(R)-VU 6008667
T12647CAS 2097818-14-7
(R)-VU 6008667 is devoid of M5 NAM activity (IC50>10 μM).