Comparison

Molecules

2174763 Item(s)

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Name PDF Type Clone Specific against Appl. Host Item no. Amount Price
Ro 5212773 Chemicals Other EPPTB is a selective antagonist of the trace amine-associated receptor 1 (TAAR1). DCC-DC21573-100mg

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Ro 5212773 Chemicals Other EPPTB is a selective antagonist of the trace amine-associated receptor 1 (TAAR1). DCC-DC21573-250mg

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Ro 5212773 Chemicals Other EPPTB is a selective antagonist of the trace amine-associated receptor 1 (TAAR1). DCC-DC21573-1g

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BIBO-­3304 Chemicals Other IC DCC-DC20788-100mg

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100 mg Login
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BIBO-­3304 Chemicals Other IC DCC-DC20788-250mg

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250 mg Login
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BIBO-­3304 Chemicals Other IC DCC-DC20788-1g

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1 g Login
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Sephin 1 Chemicals Other other DCC-DC21409-100mg

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100 mg Login
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Sephin 1 Chemicals Other other DCC-DC21409-250mg

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Sephin 1 Chemicals Other other DCC-DC21409-1g

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AT-­130 Chemicals Other IC DCC-DC20699-100mg

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AT-­130 Chemicals Other IC DCC-DC20699-250mg

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AT-­130 Chemicals Other IC DCC-DC20699-1g

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ABL127 Chemicals Other IC DCC-DC20619-5mg

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Rupintrivir Chemicals Other Rupintrivir (AG-7088, AG7088) is a potent, irreversible inhibitor of human rhinovirus 3C protease, inhibits the replication of all HRV serotypes with EC50 of 23 nM and EC90 of 82 nM. DCC-DC20647-25mg

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AM1241 Chemicals Other A potent, selective cannabinoid receptor CB2 agonist with Ki of 7.1 nM, >80-fold selectivity over CB1 receptors in radioligand binding assay. DCC-DC20658-100mg

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AM1241 Chemicals Other A potent, selective cannabinoid receptor CB2 agonist with Ki of 7.1 nM, >80-fold selectivity over CB1 receptors in radioligand binding assay. DCC-DC20658-250mg

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AM1241 Chemicals Other A potent, selective cannabinoid receptor CB2 agonist with Ki of 7.1 nM, >80-fold selectivity over CB1 receptors in radioligand binding assay. DCC-DC20658-1g

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CAN-­508 Chemicals Other IC DCC-DC20859-100mg

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CAN-­508 Chemicals Other IC DCC-DC20859-250mg

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CAN-­508 Chemicals Other IC DCC-DC20859-1g

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NKH 477 hydrochloride Chemicals Other NKH 477 hydrochloride (Colforsin dapropate) is a water-soluble analog of Forskolin and a potent activator of adenylyl cyclase, shows some selectivity for cardiac (type V) adenylyl cyclase. DCC-DC20916-10mg

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JNJ-­47965567 Chemicals Other respectively., selective, JNJ-47965567 is a potent, centrally permeable P2X7 receptor antagonist with pKi of 7.9 and 8.7 for human and rat P2X7 DCC-DC21180-100mg

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JNJ-­47965567 Chemicals Other respectively., selective, JNJ-47965567 is a potent, centrally permeable P2X7 receptor antagonist with pKi of 7.9 and 8.7 for human and rat P2X7 DCC-DC21180-250mg

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JNJ-­47965567 Chemicals Other respectively., selective, JNJ-47965567 is a potent, centrally permeable P2X7 receptor antagonist with pKi of 7.9 and 8.7 for human and rat P2X7 DCC-DC21180-1g

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KT-­109 Chemicals Other IC DCC-DC21205-25mg

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Name Price
Ro 5212773 Login
Type Chemicals
Clone
Specific against Other
Appl. EPPTB is a selective antagonist of the trace amine-associated receptor 1 (TAAR1).
Host
Item no.
Amount 100 mg
Available
Ro 5212773 Login
Type Chemicals
Clone
Specific against Other
Appl. EPPTB is a selective antagonist of the trace amine-associated receptor 1 (TAAR1).
Host
Item no.
Amount 250 mg
Available
Ro 5212773 Login
Type Chemicals
Clone
Specific against Other
Appl. EPPTB is a selective antagonist of the trace amine-associated receptor 1 (TAAR1).
Host
Item no.
Amount 1 g
Available
BIBO-­3304 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 100 mg
Available
BIBO-­3304 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 250 mg
Available
BIBO-­3304 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 1 g
Available
Sephin 1 Login
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 100 mg
Available
Sephin 1 Login
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 250 mg
Available
Sephin 1 Login
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 1 g
Available
AT-­130 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 100 mg
Available
AT-­130 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 250 mg
Available
AT-­130 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 1 g
Available
ABL127 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 5 mg
Available
Rupintrivir Login
Type Chemicals
Clone
Specific against Other
Appl. Rupintrivir (AG-7088, AG7088) is a potent, irreversible inhibitor of human rhinovirus 3C protease, inhibits the replication of all HRV serotypes with EC50 of 23 nM and EC90 of 82 nM.
Host
Item no.
Amount 25 mg
Available
AM1241 Login
Type Chemicals
Clone
Specific against Other
Appl. A potent, selective cannabinoid receptor CB2 agonist with Ki of 7.1 nM, >80-fold selectivity over CB1 receptors in radioligand binding assay.
Host
Item no.
Amount 100 mg
Available
AM1241 Login
Type Chemicals
Clone
Specific against Other
Appl. A potent, selective cannabinoid receptor CB2 agonist with Ki of 7.1 nM, >80-fold selectivity over CB1 receptors in radioligand binding assay.
Host
Item no.
Amount 250 mg
Available
AM1241 Login
Type Chemicals
Clone
Specific against Other
Appl. A potent, selective cannabinoid receptor CB2 agonist with Ki of 7.1 nM, >80-fold selectivity over CB1 receptors in radioligand binding assay.
Host
Item no.
Amount 1 g
Available
CAN-­508 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 100 mg
Available
CAN-­508 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 250 mg
Available
CAN-­508 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 1 g
Available
NKH 477 hydrochloride Login
Type Chemicals
Clone
Specific against Other
Appl. NKH 477 hydrochloride (Colforsin dapropate) is a water-soluble analog of Forskolin and a potent activator of adenylyl cyclase, shows some selectivity for cardiac (type V) adenylyl cyclase.
Host
Item no.
Amount 10 mg
Available
JNJ-­47965567 Login
Type Chemicals
Clone
Specific against Other
Appl. respectively., selective, JNJ-47965567 is a potent, centrally permeable P2X7 receptor antagonist with pKi of 7.9 and 8.7 for human and rat P2X7
Host
Item no.
Amount 100 mg
Available
JNJ-­47965567 Login
Type Chemicals
Clone
Specific against Other
Appl. respectively., selective, JNJ-47965567 is a potent, centrally permeable P2X7 receptor antagonist with pKi of 7.9 and 8.7 for human and rat P2X7
Host
Item no.
Amount 250 mg
Available
JNJ-­47965567 Login
Type Chemicals
Clone
Specific against Other
Appl. respectively., selective, JNJ-47965567 is a potent, centrally permeable P2X7 receptor antagonist with pKi of 7.9 and 8.7 for human and rat P2X7
Host
Item no.
Amount 1 g
Available
KT-­109 Login
Type Chemicals
Clone
Specific against Other
Appl. IC
Host
Item no.
Amount 25 mg
Available

2174763 Item(s)

per page