TargetMol

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Target Molecule Corp. (TargetMol) is a global high-tech enterprise, specializing in chemical and biological research products and service to meet the research needs of global customers. With the help of fast and efficient global supply chain,professional and rigorous procurement process and timely dynamic news of products, you will save more time with less cost and lead in drug discovery and screening. We are equipped to meet an array of client’s requirements, varying from virtual screening to chemical structure optimization to the provision of commercial products. For further information on our products and services, take a look around our website.

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(+)-Mk-801 Maleate 25mg  | 99.00%

TargetMol

(+)-MK-801 is a potent noncompetitive antagonist of the NMDA receptor (RECEPTORS, N-METHYL-D-ASPARTATE) with Kd of 37.2 nM in rat brain membranes. The drug has been considered for the wide variety of neurodegenerative conditions or disorders in which NMDA receptors may play an important role.

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(+)-Mk-801 Maleate 50mg  | 99.00%

TargetMol

(+)-MK-801 is a potent noncompetitive antagonist of the NMDA receptor (RECEPTORS, N-METHYL-D-ASPARTATE) with Kd of 37.2 nM in rat brain membranes. The drug has been considered for the wide variety of neurodegenerative conditions or disorders in which NMDA receptors may play an important role.

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(+)-Shikonin 10mM * 1mL (in DMSO)  | 98.00%

TargetMol

Shikonin is an TMEM16A chloride channel inhibitor (IC50: 6.5 μM). Shikonin is also a selective PKM2 inhibitor and can also suppress activation of the NF-κB pathway and inhibit TNF-α.

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(+)-Shikonin 200mg  | 98.00%

TargetMol

Shikonin is an TMEM16A chloride channel inhibitor (IC50: 6.5 μM). Shikonin is also a selective PKM2 inhibitor and can also suppress activation of the NF-κB pathway and inhibit TNF-α.

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(+)-Shikonin 10mg  | 98.00%

TargetMol

Shikonin is an TMEM16A chloride channel inhibitor (IC50: 6.5 μM). Shikonin is also a selective PKM2 inhibitor and can also suppress activation of the NF-κB pathway and inhibit TNF-α.

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(+)-Shikonin 25mg  | 98.00%

TargetMol

Shikonin is an TMEM16A chloride channel inhibitor (IC50: 6.5 μM). Shikonin is also a selective PKM2 inhibitor and can also suppress activation of the NF-κB pathway and inhibit TNF-α.

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(+)-Shikonin 50mg  | 98.00%

TargetMol

Shikonin is an TMEM16A chloride channel inhibitor (IC50: 6.5 μM). Shikonin is also a selective PKM2 inhibitor and can also suppress activation of the NF-κB pathway and inhibit TNF-α.

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(+)-Shikonin 100mg  | 98.00%

TargetMol

Shikonin is an TMEM16A chloride channel inhibitor (IC50: 6.5 μM). Shikonin is also a selective PKM2 inhibitor and can also suppress activation of the NF-κB pathway and inhibit TNF-α.

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(±) Clopidogrel hydrogensulfate 50mg  | 99.04%

TargetMol

Clopidogrel, an antiplatelet agent pharmacologically and structurally analogous to ticlopidine, is used to inhibit blood clots in various conditions such as cerebrovascular disease, peripheral vascular disease, and coronary artery disease.

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(±) Clopidogrel hydrogensulfate 100mg  | 99.04%

TargetMol

Clopidogrel, an antiplatelet agent pharmacologically and structurally analogous to ticlopidine, is used to inhibit blood clots in various conditions such as cerebrovascular disease, peripheral vascular disease, and coronary artery disease.

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(±) Clopidogrel hydrogensulfate 500mg  | 99.04%

TargetMol

Clopidogrel, an antiplatelet agent pharmacologically and structurally analogous to ticlopidine, is used to inhibit blood clots in various conditions such as cerebrovascular disease, peripheral vascular disease, and coronary artery disease.

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(±) Clopidogrel hydrogensulfate 10mM * 1mL (in DMSO)  | 99.04%

TargetMol

Clopidogrel, an antiplatelet agent pharmacologically and structurally analogous to ticlopidine, is used to inhibit blood clots in various conditions such as cerebrovascular disease, peripheral vascular disease, and coronary artery disease.

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(±)-Bisoprolol hemifumarate 100mg  | 99.00%

TargetMol

Bisoprolol,a selective beta-1 adrenergic receptor antagonist,selectively and competitively binds to and blocks beta-1 adrenergic receptors in the heart,thereby with antihypertensive activity and devoid of intrinsic sympathomimetic activity.

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(±)-Bisoprolol hemifumarate 200mg  | 99.00%

TargetMol

Bisoprolol,a selective beta-1 adrenergic receptor antagonist,selectively and competitively binds to and blocks beta-1 adrenergic receptors in the heart,thereby with antihypertensive activity and devoid of intrinsic sympathomimetic activity.

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(±)-Bisoprolol hemifumarate 500mg  | 99.00%

TargetMol

Bisoprolol,a selective beta-1 adrenergic receptor antagonist,selectively and competitively binds to and blocks beta-1 adrenergic receptors in the heart,thereby with antihypertensive activity and devoid of intrinsic sympathomimetic activity.

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(±)-Bisoprolol hemifumarate 10mM * 1mL (in DMSO)  | 99.00%

TargetMol

Bisoprolol,a selective beta-1 adrenergic receptor antagonist,selectively and competitively binds to and blocks beta-1 adrenergic receptors in the heart,thereby with antihypertensive activity and devoid of intrinsic sympathomimetic activity.

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(±)-Equol 5mg  | 98.28%

TargetMol

Equol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora. The estrogen receptor (ER) agonist activity of the naturally occurring (S)-enantiomer (EC50 = 85 and 65 nM for human ERα and ERβ, respectively) is similar to that of genistein but exceeds that of daidzein. (S)-Equol preferentially binds ERβ (Ki = 0.73 […]

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(±)-Equol 10mg  | 98.28%

TargetMol

Equol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora. The estrogen receptor (ER) agonist activity of the naturally occurring (S)-enantiomer (EC50 = 85 and 65 nM for human ERα and ERβ, respectively) is similar to that of genistein but exceeds that of daidzein. (S)-Equol preferentially binds ERβ (Ki = 0.73 […]

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(±)-Equol 25mg  | 98.28%

TargetMol

Equol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora. The estrogen receptor (ER) agonist activity of the naturally occurring (S)-enantiomer (EC50 = 85 and 65 nM for human ERα and ERβ, respectively) is similar to that of genistein but exceeds that of daidzein. (S)-Equol preferentially binds ERβ (Ki = 0.73 […]

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(±)-Equol 50mg  | 98.28%

TargetMol

Equol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora. The estrogen receptor (ER) agonist activity of the naturally occurring (S)-enantiomer (EC50 = 85 and 65 nM for human ERα and ERβ, respectively) is similar to that of genistein but exceeds that of daidzein. (S)-Equol preferentially binds ERβ (Ki = 0.73 […]

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(±)-Equol 100mg  | 98.28%

TargetMol

Equol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora. The estrogen receptor (ER) agonist activity of the naturally occurring (S)-enantiomer (EC50 = 85 and 65 nM for human ERα and ERβ, respectively) is similar to that of genistein but exceeds that of daidzein. (S)-Equol preferentially binds ERβ (Ki = 0.73 […]

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(±)-Equol 200mg  | 98.28%

TargetMol

Equol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora. The estrogen receptor (ER) agonist activity of the naturally occurring (S)-enantiomer (EC50 = 85 and 65 nM for human ERα and ERβ, respectively) is similar to that of genistein but exceeds that of daidzein. (S)-Equol preferentially binds ERβ (Ki = 0.73 […]

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(±)-Equol 10mM * 1mL (in DMSO)  | 98.28%

TargetMol

Equol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora. The estrogen receptor (ER) agonist activity of the naturally occurring (S)-enantiomer (EC50 = 85 and 65 nM for human ERα and ERβ, respectively) is similar to that of genistein but exceeds that of daidzein. (S)-Equol preferentially binds ERβ (Ki = 0.73 […]

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(±)-trans-ACPD 2mg  | 99.53%

TargetMol

(±)-trans-ACPD is an equimolecular mixture of (1S,3R)- and (1R,3S)-ACPD. (±)-trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).

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(±)-trans-ACPD 5mg  | 99.53%

TargetMol

(±)-trans-ACPD is an equimolecular mixture of (1S,3R)- and (1R,3S)-ACPD. (±)-trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).

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(±)-trans-ACPD 10mg  | 99.53%

TargetMol

(±)-trans-ACPD is an equimolecular mixture of (1S,3R)- and (1R,3S)-ACPD. (±)-trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).

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(±)-trans-ACPD 25mg  | 99.53%

TargetMol

(±)-trans-ACPD is an equimolecular mixture of (1S,3R)- and (1R,3S)-ACPD. (±)-trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).

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(±)-trans-ACPD 50mg  | 99.53%

TargetMol

(±)-trans-ACPD is an equimolecular mixture of (1S,3R)- and (1R,3S)-ACPD. (±)-trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).

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(±)-trans-ACPD 100mg  | 99.53%

TargetMol

(±)-trans-ACPD is an equimolecular mixture of (1S,3R)- and (1R,3S)-ACPD. (±)-trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).

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(±)Shikonin 10mM * 1mL (in DMSO)  | 98.00%

TargetMol

Red dye component of alkanet root extract used for coloring sausage casings, margarine, confectionery and wine.

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