Comparison

Molecules

2174763 Item(s)

per page

Name PDF Type Clone Specific against Appl. Host Item no. Amount Price
Proxalutamide Chemicals Other Proxalutamide (GT-0918) is a nonsteroidal antiandrogen (NSAA) – specifically, a selective high-affinity silent antagonist of the androgen receptor (AR) for the potential treatment of COVID-19, prostate cancer, and breast cancer. DCC-DC22771-100mg

DCChemicals
100 mg Login
Compare
Proxalutamide Chemicals Other Proxalutamide (GT-0918) is a nonsteroidal antiandrogen (NSAA) – specifically, a selective high-affinity silent antagonist of the androgen receptor (AR) for the potential treatment of COVID-19, prostate cancer, and breast cancer. DCC-DC22771-250mg

DCChemicals
250 mg Login
Compare
KL001(KL-­001;KL 001) Chemicals Other KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock. DCC-DC23779-100mg

DCChemicals
100 mg Login
Compare
KL001(KL-­001;KL 001) Chemicals Other KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock. DCC-DC23779-250mg

DCChemicals
250 mg Login
Compare
KL001(KL-­001;KL 001) Chemicals Other KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock. DCC-DC23779-1g

DCChemicals
1 g Login
Compare
R788 disodium hexahydrate Chemicals Other IC DCC-DC23114-100mg

DCChemicals
100 mg Login
Compare
Aplaviroc HCl Chemicals Other Cell Culture DCC-DC23522-100mg

DCChemicals
100 mg Login
Compare
Aplaviroc HCl Chemicals Other Cell Culture DCC-DC23522-250mg

DCChemicals
250 mg Login
Compare
Aplaviroc HCl Chemicals Other Cell Culture DCC-DC23522-1g

DCChemicals
1 g Login
Compare
Lumateperone Chemicals Other Lumateperone (ITI-007) is a potent 5-HT2A antagonist (Ki=0.54 nM), postsynaptic D2 antagonist(Ki=32 nM), and SERT blocker (Ki= 61 nM). DCC-DC22906-1g

DCChemicals
1 g Login
Compare
Lumateperone Chemicals Other Lumateperone (ITI-007) is a potent 5-HT2A antagonist (Ki=0.54 nM), postsynaptic D2 antagonist(Ki=32 nM), and SERT blocker (Ki= 61 nM). DCC-DC22906-250mg

DCChemicals
250 mg Login
Compare
Lumateperone Chemicals Other Lumateperone (ITI-007) is a potent 5-HT2A antagonist (Ki=0.54 nM), postsynaptic D2 antagonist(Ki=32 nM), and SERT blocker (Ki= 61 nM). DCC-DC22906-100mg

DCChemicals
100 mg Login
Compare
CPYPP Chemicals Other IC DCC-DC23765-100mg

DCChemicals
100 mg Login
Compare
CPYPP Chemicals Other IC DCC-DC23765-250mg

DCChemicals
250 mg Login
Compare
CPYPP Chemicals Other IC DCC-DC23765-1g

DCChemicals
1 g Login
Compare
Nalfurafine Chemicals Other respectively)., Nalfurafine (TRK-820, TRK820) is potent, selective agonist of kappa-opioid receptor with Ki of 3.5 nM, 15-fold less potent for μOR and little affinity for δOR (Ki=53 and 1, 200 nM DCC-DC23102-100mg

DCChemicals
100 mg Login
Compare
Nalfurafine Chemicals Other respectively)., Nalfurafine (TRK-820, TRK820) is potent, selective agonist of kappa-opioid receptor with Ki of 3.5 nM, 15-fold less potent for μOR and little affinity for δOR (Ki=53 and 1, 200 nM DCC-DC23102-250mg

DCChemicals
250 mg Login
Compare
Nalfurafine Chemicals Other respectively)., Nalfurafine (TRK-820, TRK820) is potent, selective agonist of kappa-opioid receptor with Ki of 3.5 nM, 15-fold less potent for μOR and little affinity for δOR (Ki=53 and 1, 200 nM DCC-DC23102-1g

DCChemicals
1 g Login
Compare
R-­59949(R-­59-­949) Chemicals Other IC DCC-DC23010-100mg

DCChemicals
100 mg Login
Compare
R-­59949(R-­59-­949) Chemicals Other IC DCC-DC23010-250mg

DCChemicals
250 mg Login
Compare
R-­59949(R-­59-­949) Chemicals Other IC DCC-DC23010-1g

DCChemicals
1 g Login
Compare
Gemigliptin Chemicals Other selective, A novel potent, competitive and orally active DPP4 inhibitor with potential for the treatment of type 2 diabetes. DCC-DC23672-100mg

DCChemicals
100 mg Login
Compare
Gemigliptin Chemicals Other selective, A novel potent, competitive and orally active DPP4 inhibitor with potential for the treatment of type 2 diabetes. DCC-DC23672-250mg

DCChemicals
250 mg Login
Compare
Gemigliptin Chemicals Other selective, A novel potent, competitive and orally active DPP4 inhibitor with potential for the treatment of type 2 diabetes. DCC-DC23672-1g

DCChemicals
1 g Login
Compare
Naspm trihydrochloride Chemicals Other IC DCC-DC23157-100mg

DCChemicals
100 mg Login
Compare
Name Price
Proxalutamide Login
Type Chemicals
Clone
Specific against Other
Appl. Proxalutamide (GT-0918) is a nonsteroidal antiandrogen (NSAA) – specifically, a selective high-affinity silent antagonist of the androgen receptor (AR) for the potential treatment of COVID-19, prostate cancer, and breast cancer.
Host
Item no.
Amount 100 mg
Available
Proxalutamide Login
Type Chemicals
Clone
Specific against Other
Appl. Proxalutamide (GT-0918) is a nonsteroidal antiandrogen (NSAA) – specifically, a selective high-affinity silent antagonist of the androgen receptor (AR) for the potential treatment of COVID-19, prostate cancer, and breast cancer.
Host
Item no.
Amount 250 mg
Available
KL001(KL-­001;KL 001) Login
Type Chemicals
Clone
Specific against Other
Appl. KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock.
Host
Item no.
Amount 100 mg
Available
KL001(KL-­001;KL 001) Login
Type Chemicals
Clone
Specific against Other
Appl. KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock.
Host
Item no.
Amount 250 mg
Available
KL001(KL-­001;KL 001) Login
Type Chemicals
Clone
Specific against Other
Appl. KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock.
Host
Item no.
Amount 1 g
Available
R788 disodium hexahydrate Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 100 mg
Available
Aplaviroc HCl Login
Type Chemicals
Clone
Specific against Other
Appl. Cell Culture
Host
Item no.
Amount 100 mg
Available
Aplaviroc HCl Login
Type Chemicals
Clone
Specific against Other
Appl. Cell Culture
Host
Item no.
Amount 250 mg
Available
Aplaviroc HCl Login
Type Chemicals
Clone
Specific against Other
Appl. Cell Culture
Host
Item no.
Amount 1 g
Available
Lumateperone Login
Type Chemicals
Clone
Specific against Other
Appl. Lumateperone (ITI-007) is a potent 5-HT2A antagonist (Ki=0.54 nM), postsynaptic D2 antagonist(Ki=32 nM), and SERT blocker (Ki= 61 nM).
Host
Item no.
Amount 1 g
Available
Lumateperone Login
Type Chemicals
Clone
Specific against Other
Appl. Lumateperone (ITI-007) is a potent 5-HT2A antagonist (Ki=0.54 nM), postsynaptic D2 antagonist(Ki=32 nM), and SERT blocker (Ki= 61 nM).
Host
Item no.
Amount 250 mg
Available
Lumateperone Login
Type Chemicals
Clone
Specific against Other
Appl. Lumateperone (ITI-007) is a potent 5-HT2A antagonist (Ki=0.54 nM), postsynaptic D2 antagonist(Ki=32 nM), and SERT blocker (Ki= 61 nM).
Host
Item no.
Amount 100 mg
Available
CPYPP Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 100 mg
Available
CPYPP Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 250 mg
Available
CPYPP Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 1 g
Available
Nalfurafine Login
Type Chemicals
Clone
Specific against Other
Appl. respectively)., Nalfurafine (TRK-820, TRK820) is potent, selective agonist of kappa-opioid receptor with Ki of 3.5 nM, 15-fold less potent for μOR and little affinity for δOR (Ki=53 and 1, 200 nM
Host
Item no.
Amount 100 mg
Available
Nalfurafine Login
Type Chemicals
Clone
Specific against Other
Appl. respectively)., Nalfurafine (TRK-820, TRK820) is potent, selective agonist of kappa-opioid receptor with Ki of 3.5 nM, 15-fold less potent for μOR and little affinity for δOR (Ki=53 and 1, 200 nM
Host
Item no.
Amount 250 mg
Available
Nalfurafine Login
Type Chemicals
Clone
Specific against Other
Appl. respectively)., Nalfurafine (TRK-820, TRK820) is potent, selective agonist of kappa-opioid receptor with Ki of 3.5 nM, 15-fold less potent for μOR and little affinity for δOR (Ki=53 and 1, 200 nM
Host
Item no.
Amount 1 g
Available
R-­59949(R-­59-­949) Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 100 mg
Available
R-­59949(R-­59-­949) Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 250 mg
Available
R-­59949(R-­59-­949) Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 1 g
Available
Gemigliptin Login
Type Chemicals
Clone
Specific against Other
Appl. selective, A novel potent, competitive and orally active DPP4 inhibitor with potential for the treatment of type 2 diabetes.
Host
Item no.
Amount 100 mg
Available
Gemigliptin Login
Type Chemicals
Clone
Specific against Other
Appl. selective, A novel potent, competitive and orally active DPP4 inhibitor with potential for the treatment of type 2 diabetes.
Host
Item no.
Amount 250 mg
Available
Gemigliptin Login
Type Chemicals
Clone
Specific against Other
Appl. selective, A novel potent, competitive and orally active DPP4 inhibitor with potential for the treatment of type 2 diabetes.
Host
Item no.
Amount 1 g
Available
Naspm trihydrochloride Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 100 mg
Available

2174763 Item(s)

per page