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1437732 Item(s)

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  2. 41
  3. 42
  4. 43
  5. 44
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
Difelikefalin HCl Chemicals Other Difelikefalin is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Di DCC-DC60186-100mg

DCChemicals 		100 mg Login
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Difelikefalin HCl Chemicals Other Difelikefalin is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Di DCC-DC60186-250mg

DCChemicals 		250 mg Login
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Difelikefalin HCl Chemicals Other Difelikefalin is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Di DCC-DC60186-1g

DCChemicals 		1 g Login
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AZ194 Chemicals Other HUN51998, also known as CRMP2-Ubc9-NaV1.7 inhibitor 194, is a CRMP2-Ubc9-NaV1.7 inhibitor. HUN51998 was first reported in patent WO 2018144900, which functioned as a antagonist of small ubiquitin like modifier (SUMO) related modification (SUMOylation) of collapsin response mediator protein 2 (CRMP2)​ with potential application for the treatment of voltage gated sodium channel 1.7 (Nav1.7) related, anosmia, migraine event, and​/or pain (e.g., neuropathic pain). DCC-DC60184-100mg

DCChemicals 		100 mg Login
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AZ194 Chemicals Other HUN51998, also known as CRMP2-Ubc9-NaV1.7 inhibitor 194, is a CRMP2-Ubc9-NaV1.7 inhibitor. HUN51998 was first reported in patent WO 2018144900, anosmia, migraine event, and​/or pain (e.g., neuropathic pain)., which functioned as a antagonist of small ubiquitin like modifier (SUMO) related modification (SUMOylation) of collapsin response mediator protein 2 (CRMP2)​ with potential application for the treatment of voltage gated sodium channel 1.7 (Nav1.7) related DCC-DC60184-250mg

DCChemicals 		250 mg Login
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AZ194 Chemicals Other HUN51998, also known as CRMP2-Ubc9-NaV1.7 inhibitor 194, is a CRMP2-Ubc9-NaV1.7 inhibitor. HUN51998 was first reported in patent WO 2018144900, anosmia, migraine event, and​/or pain (e.g., neuropathic pain)., which functioned as a antagonist of small ubiquitin like modifier (SUMO) related modification (SUMOylation) of collapsin response mediator protein 2 (CRMP2)​ with potential application for the treatment of voltage gated sodium channel 1.7 (Nav1.7) related DCC-DC60184-1g

DCChemicals 		1 g Login
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NSC2805 Chemicals Other NSC-2805 is a WWP2 ubiquitin ligase inhibitor. DCC-DC60161-100mg

DCChemicals 		100 mg Login
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NSC2805 Chemicals Other NSC-2805 is a WWP2 ubiquitin ligase inhibitor. DCC-DC60161-250mg

DCChemicals 		250 mg Login
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NSC2805 Chemicals Other NSC-2805 is a WWP2 ubiquitin ligase inhibitor. DCC-DC60161-1g

DCChemicals 		1 g Login
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CAY10526 Chemicals Other other DCC-DC60174-100mg

DCChemicals 		100 mg Login
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CAY10526 Chemicals Other other DCC-DC60174-250mg

DCChemicals 		250 mg Login
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CAY10526 Chemicals Other other DCC-DC60174-1g

DCChemicals 		1 g Login
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Camibirstat (FHD-­286) Chemicals Other FHD286(FHD 286 ) is a BRG1/BRM ATPase inhibitor for the treatment of BAF-related disorders such as acute myeloid leukemia. DCC-DC60219-100mg

DCChemicals 		100 mg Login
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Camibirstat (FHD-­286) Chemicals Other FHD286(FHD 286 ) is a BRG1/BRM ATPase inhibitor for the treatment of BAF-related disorders such as acute myeloid leukemia. DCC-DC60219-250mg

DCChemicals 		250 mg Login
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Camibirstat (FHD-­286) Chemicals Other FHD286(FHD 286 ) is a BRG1/BRM ATPase inhibitor for the treatment of BAF-related disorders such as acute myeloid leukemia. DCC-DC60219-1g

DCChemicals 		1 g Login
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PKCiota-­IN-­49 Chemicals Other DCC-DC60309-100mg

DCChemicals 		100 mg Login
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PKCiota-­IN-­49 Chemicals Other DCC-DC60309-250mg

DCChemicals 		250 mg Login
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PKCiota-­IN-­49 Chemicals Other DCC-DC60309-1g

DCChemicals 		1 g Login
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5-­HT3 antagonist 5 Chemicals Other 5-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound, a 5-HT3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT3 agonist and 2-methyl-5-HT, and shows anti-depressant effect in mice[1]. DCC-DC60308-100mg

DCChemicals 		100 mg Login
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5-­HT3 antagonist 5 Chemicals Other 5-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound, a 5-HT3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT3 agonist and 2-methyl-5-HT, and shows anti-depressant effect in mice[1]. DCC-DC60308-250mg

DCChemicals 		250 mg Login
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5-­HT3 antagonist 5 Chemicals Other 5-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound, a 5-HT3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT3 agonist and 2-methyl-5-HT, and shows anti-depressant effect in mice[1]. DCC-DC60308-1g

DCChemicals 		1 g Login
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WAY323096 Chemicals Other DCC-DC60307-100mg

DCChemicals 		100 mg Login
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WAY323096 Chemicals Other DCC-DC60307-250mg

DCChemicals 		250 mg Login
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WAY323096 Chemicals Other DCC-DC60307-1g

DCChemicals 		1 g Login
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ESI-­08 Chemicals Other DCC-DC60306-100mg

DCChemicals 		100 mg Login
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Name Price
Difelikefalin HCl Login Difelikefalin HCl
Type Chemicals
Clone
Specific against Other
Appl. Difelikefalin is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Di
Host
Item no.
Amount 100 mg
Available
Difelikefalin HCl Login Difelikefalin HCl
Type Chemicals
Clone
Specific against Other
Appl. Difelikefalin is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Di
Host
Item no.
Amount 250 mg
Available
Difelikefalin HCl Login Difelikefalin HCl
Type Chemicals
Clone
Specific against Other
Appl. Difelikefalin is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Di
Host
Item no.
Amount 1 g
Available
AZ194 Login AZ194
Type Chemicals
Clone
Specific against Other
Appl. HUN51998, also known as CRMP2-Ubc9-NaV1.7 inhibitor 194, is a CRMP2-Ubc9-NaV1.7 inhibitor. HUN51998 was first reported in patent WO 2018144900, which functioned as a antagonist of small ubiquitin like modifier (SUMO) related modification (SUMOylation) of collapsin response mediator protein 2 (CRMP2)​ with potential application for the treatment of voltage gated sodium channel 1.7 (Nav1.7) related, anosmia, migraine event, and​/or pain (e.g., neuropathic pain).
Host
Item no.
Amount 100 mg
Available
AZ194 Login AZ194
Type Chemicals
Clone
Specific against Other
Appl. HUN51998, also known as CRMP2-Ubc9-NaV1.7 inhibitor 194, is a CRMP2-Ubc9-NaV1.7 inhibitor. HUN51998 was first reported in patent WO 2018144900, anosmia, migraine event, and​/or pain (e.g., neuropathic pain)., which functioned as a antagonist of small ubiquitin like modifier (SUMO) related modification (SUMOylation) of collapsin response mediator protein 2 (CRMP2)​ with potential application for the treatment of voltage gated sodium channel 1.7 (Nav1.7) related
Host
Item no.
Amount 250 mg
Available
AZ194 Login AZ194
Type Chemicals
Clone
Specific against Other
Appl. HUN51998, also known as CRMP2-Ubc9-NaV1.7 inhibitor 194, is a CRMP2-Ubc9-NaV1.7 inhibitor. HUN51998 was first reported in patent WO 2018144900, anosmia, migraine event, and​/or pain (e.g., neuropathic pain)., which functioned as a antagonist of small ubiquitin like modifier (SUMO) related modification (SUMOylation) of collapsin response mediator protein 2 (CRMP2)​ with potential application for the treatment of voltage gated sodium channel 1.7 (Nav1.7) related
Host
Item no.
Amount 1 g
Available
NSC2805 Login NSC2805
Type Chemicals
Clone
Specific against Other
Appl. NSC-2805 is a WWP2 ubiquitin ligase inhibitor.
Host
Item no.
Amount 100 mg
Available
NSC2805 Login NSC2805
Type Chemicals
Clone
Specific against Other
Appl. NSC-2805 is a WWP2 ubiquitin ligase inhibitor.
Host
Item no.
Amount 250 mg
Available
NSC2805 Login NSC2805
Type Chemicals
Clone
Specific against Other
Appl. NSC-2805 is a WWP2 ubiquitin ligase inhibitor.
Host
Item no.
Amount 1 g
Available
CAY10526 Login CAY10526
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 100 mg
Available
CAY10526 Login CAY10526
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 250 mg
Available
CAY10526 Login CAY10526
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 1 g
Available
Camibirstat (FHD-­286) Login Camibirstat (FHD-286)
Type Chemicals
Clone
Specific against Other
Appl. FHD286(FHD 286 ) is a BRG1/BRM ATPase inhibitor for the treatment of BAF-related disorders such as acute myeloid leukemia.
Host
Item no.
Amount 100 mg
Available
Camibirstat (FHD-­286) Login Camibirstat (FHD-286)
Type Chemicals
Clone
Specific against Other
Appl. FHD286(FHD 286 ) is a BRG1/BRM ATPase inhibitor for the treatment of BAF-related disorders such as acute myeloid leukemia.
Host
Item no.
Amount 250 mg
Available
Camibirstat (FHD-­286) Login Camibirstat (FHD-286)
Type Chemicals
Clone
Specific against Other
Appl. FHD286(FHD 286 ) is a BRG1/BRM ATPase inhibitor for the treatment of BAF-related disorders such as acute myeloid leukemia.
Host
Item no.
Amount 1 g
Available
PKCiota-­IN-­49 Login PKCiota-IN-49
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
PKCiota-­IN-­49 Login PKCiota-IN-49
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 250 mg
Available
PKCiota-­IN-­49 Login PKCiota-IN-49
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
5-­HT3 antagonist 5 Login 5-HT3 antagonist 5
Type Chemicals
Clone
Specific against Other
Appl. 5-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound, a 5-HT3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT3 agonist and 2-methyl-5-HT, and shows anti-depressant effect in mice[1].
Host
Item no.
Amount 100 mg
Available
5-­HT3 antagonist 5 Login 5-HT3 antagonist 5
Type Chemicals
Clone
Specific against Other
Appl. 5-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound, a 5-HT3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT3 agonist and 2-methyl-5-HT, and shows anti-depressant effect in mice[1].
Host
Item no.
Amount 250 mg
Available
5-­HT3 antagonist 5 Login 5-HT3 antagonist 5
Type Chemicals
Clone
Specific against Other
Appl. 5-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound, a 5-HT3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT3 agonist and 2-methyl-5-HT, and shows anti-depressant effect in mice[1].
Host
Item no.
Amount 1 g
Available
WAY323096 Login WAY323096
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
WAY323096 Login WAY323096
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 250 mg
Available
WAY323096 Login WAY323096
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
ESI-­08 Login ESI-08
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available

1437732 Item(s)

per page

Page:
  1. 40
  2. 41
  3. 42
  4. 43
  5. 44
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