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1437732 Item(s)

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  2. 22
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  4. 24
  5. 25
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
Nifeviroc Chemicals Other Nifeviroc is a CCR5 antagonist potentially for treatment of inflammatory responses to HIV type-1 infection DCC-DC55002-1g

DCChemicals 		1 g Login
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BT-­2 Chemicals Other BT2 is a BCKDC kinase (BDK) inhibitor with an IC50 of 3.19 μM. BT2 binding to BDK triggers helix movements in the N-terminal domain, resulting in the dissociation of BDK from the branched-chain α-ketoacid dehydrogenase complex (BCKDC)[1]. BT2 (compound 4) is also a potent and selective Mcl-1 inhibitor with a Ki value of 59 μM[2]. DCC-DC55038-100mg

DCChemicals 		100 mg Login
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BT-­2 Chemicals Other BT2 is a BCKDC kinase (BDK) inhibitor with an IC50 of 3.19 μM. BT2 binding to BDK triggers helix movements in the N-terminal domain, resulting in the dissociation of BDK from the branched-chain α-ketoacid dehydrogenase complex (BCKDC)[1]. BT2 (compound 4) is also a potent and selective Mcl-1 inhibitor with a Ki value of 59 μM[2]. DCC-DC55038-250mg

DCChemicals 		250 mg Login
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BT-­2 Chemicals Other BT2 is a BCKDC kinase (BDK) inhibitor with an IC50 of 3.19 μM. BT2 binding to BDK triggers helix movements in the N-terminal domain, resulting in the dissociation of BDK from the branched-chain α-ketoacid dehydrogenase complex (BCKDC)[1]. BT2 (compound 4) is also a potent and selective Mcl-1 inhibitor with a Ki value of 59 μM[2]. DCC-DC55038-1g

DCChemicals 		1 g Login
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Sulfopin Chemicals Other IV DCC-DC53131-5mg

DCChemicals 		5 mg Login
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Gentiopicroside Chemicals Other Gentiopicroside, a naturally occurring iridoid glycoside, inhibits P450 activity, with an IC50 and a Ki of 61 µM and 22.8 µM for CYP2A6; Gentiopicroside has antianti-inflammatoryand antioxidative effects. DCC-DC55150-100mg

DCChemicals 		100 mg Login
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Gentiopicroside Chemicals Other Gentiopicroside, a naturally occurring iridoid glycoside, inhibits P450 activity, with an IC50 and a Ki of 61 µM and 22.8 µM for CYP2A6; Gentiopicroside has antianti-inflammatoryand antioxidative effects. DCC-DC55150-250mg

DCChemicals 		250 mg Login
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Gentiopicroside Chemicals Other Gentiopicroside, a naturally occurring iridoid glycoside, inhibits P450 activity, with an IC50 and a Ki of 61 µM and 22.8 µM for CYP2A6; Gentiopicroside has antianti-inflammatoryand antioxidative effects. DCC-DC55150-1g

DCChemicals 		1 g Login
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WM3835 Chemicals Other WM-3835 is a potent and high-specific HBO1 (KAT7 or MYST2) inhibitor and binds directly to the acetyl-CoA binding site of HBO1 33. WM-3835 activates apoptosis while inhibits osteosarcoma (OS) cell proliferation, migration and invasion. WM-3835 has antitumor activity and potently inhibits pOS-1 xenograft growth in mice. DCC-DC60000-100mg

DCChemicals 		100 mg Login
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WM3835 Chemicals Other WM-3835 is a potent and high-specific HBO1 (KAT7 or MYST2) inhibitor and binds directly to the acetyl-CoA binding site of HBO1 33. WM-3835 activates apoptosis while inhibits osteosarcoma (OS) cell proliferation, migration and invasion. WM-3835 has antitumor activity and potently inhibits pOS-1 xenograft growth in mice. DCC-DC60000-250mg

DCChemicals 		250 mg Login
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WM3835 Chemicals Other WM-3835 is a potent and high-specific HBO1 (KAT7 or MYST2) inhibitor and binds directly to the acetyl-CoA binding site of HBO1 33. WM-3835 activates apoptosis while inhibits osteosarcoma (OS) cell proliferation, migration and invasion. WM-3835 has antitumor activity and potently inhibits pOS-1 xenograft growth in mice. DCC-DC60000-1g

DCChemicals 		1 g Login
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CRT0036521 Chemicals Other CRT0036521 is a potent and selective inhibitor of AKR1C3. DCC-DC60005-100mg

DCChemicals 		100 mg Login
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CRT0036521 Chemicals Other CRT0036521 is a potent and selective inhibitor of AKR1C3. DCC-DC60005-250mg

DCChemicals 		250 mg Login
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CRT0036521 Chemicals Other CRT0036521 is a potent and selective inhibitor of AKR1C3. DCC-DC60005-1g

DCChemicals 		1 g Login
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BI-­0115 Chemicals Other Blocking DCC-DC59015-100mg

DCChemicals 		100 mg Login
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BI-­0115 Chemicals Other Blocking DCC-DC59015-250mg

DCChemicals 		250 mg Login
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BI-­0115 Chemicals Other Blocking DCC-DC59015-1g

DCChemicals 		1 g Login
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Org41841 Chemicals Other Org-41841 is an agonist for the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and partial agonist for TSHR. DCC-DC59012-100mg

DCChemicals 		100 mg Login
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Org41841 Chemicals Other Org-41841 is an agonist for the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and partial agonist for TSHR. DCC-DC59012-250mg

DCChemicals 		250 mg Login
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Org41841 Chemicals Other Org-41841 is an agonist for the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and partial agonist for TSHR. DCC-DC59012-1g

DCChemicals 		1 g Login
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SAR-­439859 Chemicals Other SAR439859 is an orally available, nonsteroidal selective estrogen receptor degrader/downregulator (SERD), with potential antineoplastic activity. Upon oral administration, SERD SAR439859 specifically targets and binds to the estrogen receptor (ER) and induces a conformational change that promotes ER degradation. This prevents ER-mediated signaling and inhibits both the growth and survival of ER-expressing cancer cells DCC-DC60004-100mg

DCChemicals 		100 mg Login
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SAR-­439859 Chemicals Other SAR439859 is an orally available, nonsteroidal selective estrogen receptor degrader/downregulator (SERD), with potential antineoplastic activity. Upon oral administration, SERD SAR439859 specifically targets and binds to the estrogen receptor (ER) and induces a conformational change that promotes ER degradation. This prevents ER-mediated signaling and inhibits both the growth and survival of ER-expressing cancer cells DCC-DC60004-250mg

DCChemicals 		250 mg Login
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SAR-­439859 Chemicals Other SAR439859 is an orally available, nonsteroidal selective estrogen receptor degrader/downregulator (SERD), with potential antineoplastic activity. Upon oral administration, SERD SAR439859 specifically targets and binds to the estrogen receptor (ER) and induces a conformational change that promotes ER degradation. This prevents ER-mediated signaling and inhibits both the growth and survival of ER-expressing cancer cells DCC-DC60004-1g

DCChemicals 		1 g Login
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Piperidolate Chemicals Other Piperidolate is a tertiary amine antimuscarinic. It is similar to atropine. It is mainly used in the smooth muscle spasm of the gastrointestinal tract and inhibits intestinal cramp induced by acetylcholine in rats and dogs. DCC-DC60002-100mg

DCChemicals 		100 mg Login
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Piperidolate Chemicals Other Piperidolate is a tertiary amine antimuscarinic. It is similar to atropine. It is mainly used in the smooth muscle spasm of the gastrointestinal tract and inhibits intestinal cramp induced by acetylcholine in rats and dogs. DCC-DC60002-250mg

DCChemicals 		250 mg Login
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Name Price
Nifeviroc Login Nifeviroc
Type Chemicals
Clone
Specific against Other
Appl. Nifeviroc is a CCR5 antagonist potentially for treatment of inflammatory responses to HIV type-1 infection
Host
Item no.
Amount 1 g
Available
BT-­2 Login BT-2
Type Chemicals
Clone
Specific against Other
Appl. BT2 is a BCKDC kinase (BDK) inhibitor with an IC50 of 3.19 μM. BT2 binding to BDK triggers helix movements in the N-terminal domain, resulting in the dissociation of BDK from the branched-chain α-ketoacid dehydrogenase complex (BCKDC)[1]. BT2 (compound 4) is also a potent and selective Mcl-1 inhibitor with a Ki value of 59 μM[2].
Host
Item no.
Amount 100 mg
Available
BT-­2 Login BT-2
Type Chemicals
Clone
Specific against Other
Appl. BT2 is a BCKDC kinase (BDK) inhibitor with an IC50 of 3.19 μM. BT2 binding to BDK triggers helix movements in the N-terminal domain, resulting in the dissociation of BDK from the branched-chain α-ketoacid dehydrogenase complex (BCKDC)[1]. BT2 (compound 4) is also a potent and selective Mcl-1 inhibitor with a Ki value of 59 μM[2].
Host
Item no.
Amount 250 mg
Available
BT-­2 Login BT-2
Type Chemicals
Clone
Specific against Other
Appl. BT2 is a BCKDC kinase (BDK) inhibitor with an IC50 of 3.19 μM. BT2 binding to BDK triggers helix movements in the N-terminal domain, resulting in the dissociation of BDK from the branched-chain α-ketoacid dehydrogenase complex (BCKDC)[1]. BT2 (compound 4) is also a potent and selective Mcl-1 inhibitor with a Ki value of 59 μM[2].
Host
Item no.
Amount 1 g
Available
Sulfopin Login Sulfopin
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 5 mg
Available
Gentiopicroside Login Gentiopicroside
Type Chemicals
Clone
Specific against Other
Appl. Gentiopicroside, a naturally occurring iridoid glycoside, inhibits P450 activity, with an IC50 and a Ki of 61 µM and 22.8 µM for CYP2A6; Gentiopicroside has antianti-inflammatoryand antioxidative effects.
Host
Item no.
Amount 100 mg
Available
Gentiopicroside Login Gentiopicroside
Type Chemicals
Clone
Specific against Other
Appl. Gentiopicroside, a naturally occurring iridoid glycoside, inhibits P450 activity, with an IC50 and a Ki of 61 µM and 22.8 µM for CYP2A6; Gentiopicroside has antianti-inflammatoryand antioxidative effects.
Host
Item no.
Amount 250 mg
Available
Gentiopicroside Login Gentiopicroside
Type Chemicals
Clone
Specific against Other
Appl. Gentiopicroside, a naturally occurring iridoid glycoside, inhibits P450 activity, with an IC50 and a Ki of 61 µM and 22.8 µM for CYP2A6; Gentiopicroside has antianti-inflammatoryand antioxidative effects.
Host
Item no.
Amount 1 g
Available
WM3835 Login WM3835
Type Chemicals
Clone
Specific against Other
Appl. WM-3835 is a potent and high-specific HBO1 (KAT7 or MYST2) inhibitor and binds directly to the acetyl-CoA binding site of HBO1 33. WM-3835 activates apoptosis while inhibits osteosarcoma (OS) cell proliferation, migration and invasion. WM-3835 has antitumor activity and potently inhibits pOS-1 xenograft growth in mice.
Host
Item no.
Amount 100 mg
Available
WM3835 Login WM3835
Type Chemicals
Clone
Specific against Other
Appl. WM-3835 is a potent and high-specific HBO1 (KAT7 or MYST2) inhibitor and binds directly to the acetyl-CoA binding site of HBO1 33. WM-3835 activates apoptosis while inhibits osteosarcoma (OS) cell proliferation, migration and invasion. WM-3835 has antitumor activity and potently inhibits pOS-1 xenograft growth in mice.
Host
Item no.
Amount 250 mg
Available
WM3835 Login WM3835
Type Chemicals
Clone
Specific against Other
Appl. WM-3835 is a potent and high-specific HBO1 (KAT7 or MYST2) inhibitor and binds directly to the acetyl-CoA binding site of HBO1 33. WM-3835 activates apoptosis while inhibits osteosarcoma (OS) cell proliferation, migration and invasion. WM-3835 has antitumor activity and potently inhibits pOS-1 xenograft growth in mice.
Host
Item no.
Amount 1 g
Available
CRT0036521 Login CRT0036521
Type Chemicals
Clone
Specific against Other
Appl. CRT0036521 is a potent and selective inhibitor of AKR1C3.
Host
Item no.
Amount 100 mg
Available
CRT0036521 Login CRT0036521
Type Chemicals
Clone
Specific against Other
Appl. CRT0036521 is a potent and selective inhibitor of AKR1C3.
Host
Item no.
Amount 250 mg
Available
CRT0036521 Login CRT0036521
Type Chemicals
Clone
Specific against Other
Appl. CRT0036521 is a potent and selective inhibitor of AKR1C3.
Host
Item no.
Amount 1 g
Available
BI-­0115 Login BI-0115
Type Chemicals
Clone
Specific against Other
Appl. Blocking
Host
Item no.
Amount 100 mg
Available
BI-­0115 Login BI-0115
Type Chemicals
Clone
Specific against Other
Appl. Blocking
Host
Item no.
Amount 250 mg
Available
BI-­0115 Login BI-0115
Type Chemicals
Clone
Specific against Other
Appl. Blocking
Host
Item no.
Amount 1 g
Available
Org41841 Login Org41841
Type Chemicals
Clone
Specific against Other
Appl. Org-41841 is an agonist for the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and partial agonist for TSHR.
Host
Item no.
Amount 100 mg
Available
Org41841 Login Org41841
Type Chemicals
Clone
Specific against Other
Appl. Org-41841 is an agonist for the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and partial agonist for TSHR.
Host
Item no.
Amount 250 mg
Available
Org41841 Login Org41841
Type Chemicals
Clone
Specific against Other
Appl. Org-41841 is an agonist for the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and partial agonist for TSHR.
Host
Item no.
Amount 1 g
Available
SAR-­439859 Login SAR-439859
Type Chemicals
Clone
Specific against Other
Appl. SAR439859 is an orally available, nonsteroidal selective estrogen receptor degrader/downregulator (SERD), with potential antineoplastic activity. Upon oral administration, SERD SAR439859 specifically targets and binds to the estrogen receptor (ER) and induces a conformational change that promotes ER degradation. This prevents ER-mediated signaling and inhibits both the growth and survival of ER-expressing cancer cells
Host
Item no.
Amount 100 mg
Available
SAR-­439859 Login SAR-439859
Type Chemicals
Clone
Specific against Other
Appl. SAR439859 is an orally available, nonsteroidal selective estrogen receptor degrader/downregulator (SERD), with potential antineoplastic activity. Upon oral administration, SERD SAR439859 specifically targets and binds to the estrogen receptor (ER) and induces a conformational change that promotes ER degradation. This prevents ER-mediated signaling and inhibits both the growth and survival of ER-expressing cancer cells
Host
Item no.
Amount 250 mg
Available
SAR-­439859 Login SAR-439859
Type Chemicals
Clone
Specific against Other
Appl. SAR439859 is an orally available, nonsteroidal selective estrogen receptor degrader/downregulator (SERD), with potential antineoplastic activity. Upon oral administration, SERD SAR439859 specifically targets and binds to the estrogen receptor (ER) and induces a conformational change that promotes ER degradation. This prevents ER-mediated signaling and inhibits both the growth and survival of ER-expressing cancer cells
Host
Item no.
Amount 1 g
Available
Piperidolate Login Piperidolate
Type Chemicals
Clone
Specific against Other
Appl. Piperidolate is a tertiary amine antimuscarinic. It is similar to atropine. It is mainly used in the smooth muscle spasm of the gastrointestinal tract and inhibits intestinal cramp induced by acetylcholine in rats and dogs.
Host
Item no.
Amount 100 mg
Available
Piperidolate Login Piperidolate
Type Chemicals
Clone
Specific against Other
Appl. Piperidolate is a tertiary amine antimuscarinic. It is similar to atropine. It is mainly used in the smooth muscle spasm of the gastrointestinal tract and inhibits intestinal cramp induced by acetylcholine in rats and dogs.
Host
Item no.
Amount 250 mg
Available

1437732 Item(s)

per page

Page:
  1. 21
  2. 22
  3. 23
  4. 24
  5. 25
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