Comparison

Molecules

1437732 Item(s)

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Name PDF Type Clone Specific against Appl. Host Item no. Amount Price
VH032 Chemicals Other VH-032 (VHL ligand 1) is a VHL ligand for PROTAC and potent, small molecule inhibitor of the VHL/HIF-1α interaction with Kd of 185 nM.. DCC-DC11579-250mg

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VH032 Chemicals Other VH-032 (VHL ligand 1) is a VHL ligand for PROTAC and potent, small molecule inhibitor of the VHL/HIF-1α interaction with Kd of 185 nM.. DCC-DC11579-1g

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GNE-­6776 Chemicals Other GNE-6776 is a novel potent, specific, non-covalent, orally bioavailable USP7 inhibitor with IC50 of 1.34 uM . DCC-DC11555-100mg

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GNE-­6776 Chemicals Other GNE-6776 is a novel potent, specific, non-covalent, orally bioavailable USP7 inhibitor with IC50 of 1.34 uM . DCC-DC11555-250mg

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GNE-­6776 Chemicals Other GNE-6776 is a novel potent, specific, non-covalent, orally bioavailable USP7 inhibitor with IC50 of 1.34 uM . DCC-DC11555-1g

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NNZ-­2591 Chemicals Other NNZ-2591 (cyclo-L-glycyl-L-2-allylproline)1 is an investigational synthetic analog of cyclic glycine-proline (cGP), a breakdown product of human insulin-like growth factor 1 (IGF-1), that has been chemically modified to increase its half-life, stability, and oral bioavailability. DCC-DC11386-5mg

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OTS193320 Chemicals Other OTS193320 (OTS-193320) is a potent inhibitor of protein methyltransferase SUV39H2 with IC50 of 22.2 nM. DCC-DC11256-10mg

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OTS193320 Chemicals Other OTS193320 (OTS-193320) is a potent inhibitor of protein methyltransferase SUV39H2 with IC50 of 22.2 nM. DCC-DC11256-50mg

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OTS193320 Chemicals Other OTS193320 (OTS-193320) is a potent inhibitor of protein methyltransferase SUV39H2 with IC50 of 22.2 nM. DCC-DC11256-100mg

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Cavosonstat Chemicals Other Cavosonstat is a potent, orally bioavailable inhibitor of S-nitrosoglutathione reductase (GSNOR) and CFTR modulator. DCC-DC11518-10mg

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SR-­1664 Chemicals Other IV DCC-DC11750-100mg

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SR-­1664 Chemicals Other IV DCC-DC11750-250mg

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SR-­1664 Chemicals Other IV DCC-DC11750-1g

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SB 265610 Chemicals Other SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonist. DCC-DC11978-100mg

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SB 265610 Chemicals Other SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonist. DCC-DC11978-250mg

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SB 265610 Chemicals Other SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonist. DCC-DC11978-1g

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HLY-­78 Chemicals Other HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the DIX domain of Axin and potentiates the Axin-LRP6 association to promote Wnt signaling transduction[1]. DCC-DC11651-100mg

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HLY-­78 Chemicals Other HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the DIX domain of Axin and potentiates the Axin-LRP6 association to promote Wnt signaling transduction[1]. DCC-DC11651-250mg

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HLY-­78 Chemicals Other HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the DIX domain of Axin and potentiates the Axin-LRP6 association to promote Wnt signaling transduction[1]. DCC-DC11651-1g

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PD 404182 Chemicals Other PD 404182 is a high affinity inhibitor of KDO 8-P synthase (Ki = 26 nM). Also inhibits dimethylarginine dimethylaminohydrolase 1 (DDAH1). Exhibits antiangiogenic and antiviral activity in vitro. Putative antibiotic against gram-negative bacteria. DCC-DC12012-100mg

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CC-­885 Chemicals Other ELISA, Cell Culture DCC-DC11588-100mg

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CC-­885 Chemicals Other ELISA, Cell Culture DCC-DC11588-250mg

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CC-­885 Chemicals Other ELISA, Cell Culture DCC-DC11588-1g

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RapaLink-­1 Chemicals Other RapaLink-1 is a third-generation mTOR inhibitor that overcomes resistance to existing first- and second-generation inhibitors; blocks mTOR signaling of the F2108L mTOR and M2327I mTOR drug resistant mutants; RapaLink-1 is more potent mTOR inhibitor than r DCC-DC11816-5mg

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Elsulfavirine Chemicals Other A new-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) for the treatment of HIV-1 infections, the prodrug of the active compound VM-1500A.. DCC-DC11892-100mg

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Name Price
VH032 Login
Type Chemicals
Clone
Specific against Other
Appl. VH-032 (VHL ligand 1) is a VHL ligand for PROTAC and potent, small molecule inhibitor of the VHL/HIF-1α interaction with Kd of 185 nM..
Host
Item no.
Amount 250 mg
Available
VH032 Login
Type Chemicals
Clone
Specific against Other
Appl. VH-032 (VHL ligand 1) is a VHL ligand for PROTAC and potent, small molecule inhibitor of the VHL/HIF-1α interaction with Kd of 185 nM..
Host
Item no.
Amount 1 g
Available
GNE-­6776 Login
Type Chemicals
Clone
Specific against Other
Appl. GNE-6776 is a novel potent, specific, non-covalent, orally bioavailable USP7 inhibitor with IC50 of 1.34 uM .
Host
Item no.
Amount 100 mg
Available
GNE-­6776 Login
Type Chemicals
Clone
Specific against Other
Appl. GNE-6776 is a novel potent, specific, non-covalent, orally bioavailable USP7 inhibitor with IC50 of 1.34 uM .
Host
Item no.
Amount 250 mg
Available
GNE-­6776 Login
Type Chemicals
Clone
Specific against Other
Appl. GNE-6776 is a novel potent, specific, non-covalent, orally bioavailable USP7 inhibitor with IC50 of 1.34 uM .
Host
Item no.
Amount 1 g
Available
NNZ-­2591 Login
Type Chemicals
Clone
Specific against Other
Appl. NNZ-2591 (cyclo-L-glycyl-L-2-allylproline)1 is an investigational synthetic analog of cyclic glycine-proline (cGP), a breakdown product of human insulin-like growth factor 1 (IGF-1), that has been chemically modified to increase its half-life, stability, and oral bioavailability.
Host
Item no.
Amount 5 mg
Available
OTS193320 Login
Type Chemicals
Clone
Specific against Other
Appl. OTS193320 (OTS-193320) is a potent inhibitor of protein methyltransferase SUV39H2 with IC50 of 22.2 nM.
Host
Item no.
Amount 10 mg
Available
OTS193320 Login
Type Chemicals
Clone
Specific against Other
Appl. OTS193320 (OTS-193320) is a potent inhibitor of protein methyltransferase SUV39H2 with IC50 of 22.2 nM.
Host
Item no.
Amount 50 mg
Available
OTS193320 Login
Type Chemicals
Clone
Specific against Other
Appl. OTS193320 (OTS-193320) is a potent inhibitor of protein methyltransferase SUV39H2 with IC50 of 22.2 nM.
Host
Item no.
Amount 100 mg
Available
Cavosonstat Login
Type Chemicals
Clone
Specific against Other
Appl. Cavosonstat is a potent, orally bioavailable inhibitor of S-nitrosoglutathione reductase (GSNOR) and CFTR modulator.
Host
Item no.
Amount 10 mg
Available
SR-­1664 Login
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 100 mg
Available
SR-­1664 Login
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 250 mg
Available
SR-­1664 Login
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 1 g
Available
SB 265610 Login
Type Chemicals
Clone
Specific against Other
Appl. SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonist.
Host
Item no.
Amount 100 mg
Available
SB 265610 Login
Type Chemicals
Clone
Specific against Other
Appl. SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonist.
Host
Item no.
Amount 250 mg
Available
SB 265610 Login
Type Chemicals
Clone
Specific against Other
Appl. SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonist.
Host
Item no.
Amount 1 g
Available
HLY-­78 Login
Type Chemicals
Clone
Specific against Other
Appl. HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the DIX domain of Axin and potentiates the Axin-LRP6 association to promote Wnt signaling transduction[1].
Host
Item no.
Amount 100 mg
Available
HLY-­78 Login
Type Chemicals
Clone
Specific against Other
Appl. HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the DIX domain of Axin and potentiates the Axin-LRP6 association to promote Wnt signaling transduction[1].
Host
Item no.
Amount 250 mg
Available
HLY-­78 Login
Type Chemicals
Clone
Specific against Other
Appl. HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the DIX domain of Axin and potentiates the Axin-LRP6 association to promote Wnt signaling transduction[1].
Host
Item no.
Amount 1 g
Available
PD 404182 Login
Type Chemicals
Clone
Specific against Other
Appl. PD 404182 is a high affinity inhibitor of KDO 8-P synthase (Ki = 26 nM). Also inhibits dimethylarginine dimethylaminohydrolase 1 (DDAH1). Exhibits antiangiogenic and antiviral activity in vitro. Putative antibiotic against gram-negative bacteria.
Host
Item no.
Amount 100 mg
Available
CC-­885 Login
Type Chemicals
Clone
Specific against Other
Appl. ELISA, Cell Culture
Host
Item no.
Amount 100 mg
Available
CC-­885 Login
Type Chemicals
Clone
Specific against Other
Appl. ELISA, Cell Culture
Host
Item no.
Amount 250 mg
Available
CC-­885 Login
Type Chemicals
Clone
Specific against Other
Appl. ELISA, Cell Culture
Host
Item no.
Amount 1 g
Available
RapaLink-­1 Login
Type Chemicals
Clone
Specific against Other
Appl. RapaLink-1 is a third-generation mTOR inhibitor that overcomes resistance to existing first- and second-generation inhibitors; blocks mTOR signaling of the F2108L mTOR and M2327I mTOR drug resistant mutants; RapaLink-1 is more potent mTOR inhibitor than r
Host
Item no.
Amount 5 mg
Available
Elsulfavirine Login
Type Chemicals
Clone
Specific against Other
Appl. A new-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) for the treatment of HIV-1 infections, the prodrug of the active compound VM-1500A..
Host
Item no.
Amount 100 mg
Available

1437732 Item(s)

per page