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1437732 Item(s)

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  2. 18
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  4. 20
  5. 21
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
Aminopurvalanol A Chemicals Other selective, Aminopurvalanol A is a potent, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of ph DCC-DC80011-250mg

DCChemicals 		250 mg Login
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Aminopurvalanol A Chemicals Other selective, Aminopurvalanol A is a potent, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of ph DCC-DC80011-1g

DCChemicals 		1 g Login
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Isoxicam Chemicals Other Isoxicam is an orally active, long-acting, non-steroidal anti-inflammatory agent for the research of arthritis[1]. Isoxicam is a nonselective inhibitor of COX-1 and COX-2[2]. DCC-DC80001-100mg

DCChemicals 		100 mg Login
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Isoxicam Chemicals Other Isoxicam is an orally active, long-acting, non-steroidal anti-inflammatory agent for the research of arthritis[1]. Isoxicam is a nonselective inhibitor of COX-1 and COX-2[2]. DCC-DC80001-250mg

DCChemicals 		250 mg Login
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Isoxicam Chemicals Other Isoxicam is an orally active, long-acting, non-steroidal anti-inflammatory agent for the research of arthritis[1]. Isoxicam is a nonselective inhibitor of COX-1 and COX-2[2]. DCC-DC80001-1g

DCChemicals 		1 g Login
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RX-­3117 Chemicals Other RX-3117 is an orally available and potent DNA synthesis inhibitor with potential antineoplastic activity. DCC-DC7762-100mg

DCChemicals 		100 mg Login
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RX-­3117 Chemicals Other RX-3117 is an orally available and potent DNA synthesis inhibitor with potential antineoplastic activity. DCC-DC7762-250mg

DCChemicals 		250 mg Login
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RX-­3117 Chemicals Other RX-3117 is an orally available and potent DNA synthesis inhibitor with potential antineoplastic activity. DCC-DC7762-1g

DCChemicals 		1 g Login
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PNU159682 Chemicals Other PNU-159682 is a major bioactive metabolite of Nemorubicin in human liver microsomes; > 3, 000-fold cytotoxic than its parent compound(MMDX and doxorubicin). DCC-DC7648-100mg

DCChemicals 		100 mg Login
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DTP3 Chemicals Other IV DCC-DC7849-100mg

DCChemicals 		100 mg Login
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DTP3 Chemicals Other IV DCC-DC7849-250mg

DCChemicals 		250 mg Login
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DTP3 Chemicals Other IV DCC-DC7849-1g

DCChemicals 		1 g Login
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FRAX-­486 Chemicals Other FRAX486 is a selective inhibitor of group I PAKs with IC50s of 8.25/39.5, /55.3 nM for PAK1/PAK2/PAK3 respectivelt; less potent for PAK4(IC50=779 nM). DCC-DC8003-100mg

DCChemicals 		100 mg Login
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FRAX-­486 Chemicals Other FRAX486 is a selective inhibitor of group I PAKs with IC50s of 8.25/39.5, /55.3 nM for PAK1/PAK2/PAK3 respectivelt; less potent for PAK4(IC50=779 nM). DCC-DC8003-250mg

DCChemicals 		250 mg Login
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FRAX-­486 Chemicals Other FRAX486 is a selective inhibitor of group I PAKs with IC50s of 8.25/39.5, /55.3 nM for PAK1/PAK2/PAK3 respectivelt; less potent for PAK4(IC50=779 nM). DCC-DC8003-1g

DCChemicals 		1 g Login
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BRACO19 trihydrochloride Chemicals Other BRACO19 is a telomerase inhibitor that stabilizes G-quadruplexes, targeting telomeric G-quadruplexes, inducing DNA damage and cell-cycle arrest. DCC-DC7809-100mg

DCChemicals 		100 mg Login
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BRACO19 trihydrochloride Chemicals Other BRACO19 is a telomerase inhibitor that stabilizes G-quadruplexes, targeting telomeric G-quadruplexes, inducing DNA damage and cell-cycle arrest. DCC-DC7809-250mg

DCChemicals 		250 mg Login
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BRACO19 trihydrochloride Chemicals Other BRACO19 is a telomerase inhibitor that stabilizes G-quadruplexes, targeting telomeric G-quadruplexes, inducing DNA damage and cell-cycle arrest. DCC-DC7809-1g

DCChemicals 		1 g Login
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GW-­6604 Chemicals Other GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity. DCC-DC7980-100mg

DCChemicals 		100 mg Login
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GW-­6604 Chemicals Other GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity. DCC-DC7980-250mg

DCChemicals 		250 mg Login
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GW-­6604 Chemicals Other GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity. DCC-DC7980-1g

DCChemicals 		1 g Login
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Vicriviroc maleate(Sch-­417690) Chemicals Other Vicriviroc Malate is a potent CKR-5 (CCR5) antagonist with IC50 of 0.91 nM. DCC-DC7336-100mg

DCChemicals 		100 mg Login
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Vicriviroc maleate(Sch-­417690) Chemicals Other Vicriviroc Malate is a potent CKR-5 (CCR5) antagonist with IC50 of 0.91 nM. DCC-DC7336-250mg

DCChemicals 		250 mg Login
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TAK-­242 (Resatorvid) Inhibitors Other DCC-DC7305-1g

DCChemicals 		1 g Login
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OF-­C4-­Deg-­Lin Chemicals Other DCC-DC80080-50mg

DCChemicals 		50 mg Login
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Name Price
Aminopurvalanol A Login Aminopurvalanol A
Type Chemicals
Clone
Specific against Other
Appl. selective, Aminopurvalanol A is a potent, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of ph
Host
Item no.
Amount 250 mg
Available
Aminopurvalanol A Login Aminopurvalanol A
Type Chemicals
Clone
Specific against Other
Appl. selective, Aminopurvalanol A is a potent, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of ph
Host
Item no.
Amount 1 g
Available
Isoxicam Login Isoxicam
Type Chemicals
Clone
Specific against Other
Appl. Isoxicam is an orally active, long-acting, non-steroidal anti-inflammatory agent for the research of arthritis[1]. Isoxicam is a nonselective inhibitor of COX-1 and COX-2[2].
Host
Item no.
Amount 100 mg
Available
Isoxicam Login Isoxicam
Type Chemicals
Clone
Specific against Other
Appl. Isoxicam is an orally active, long-acting, non-steroidal anti-inflammatory agent for the research of arthritis[1]. Isoxicam is a nonselective inhibitor of COX-1 and COX-2[2].
Host
Item no.
Amount 250 mg
Available
Isoxicam Login Isoxicam
Type Chemicals
Clone
Specific against Other
Appl. Isoxicam is an orally active, long-acting, non-steroidal anti-inflammatory agent for the research of arthritis[1]. Isoxicam is a nonselective inhibitor of COX-1 and COX-2[2].
Host
Item no.
Amount 1 g
Available
RX-­3117 Login RX-3117
Type Chemicals
Clone
Specific against Other
Appl. RX-3117 is an orally available and potent DNA synthesis inhibitor with potential antineoplastic activity.
Host
Item no.
Amount 100 mg
Available
RX-­3117 Login RX-3117
Type Chemicals
Clone
Specific against Other
Appl. RX-3117 is an orally available and potent DNA synthesis inhibitor with potential antineoplastic activity.
Host
Item no.
Amount 250 mg
Available
RX-­3117 Login RX-3117
Type Chemicals
Clone
Specific against Other
Appl. RX-3117 is an orally available and potent DNA synthesis inhibitor with potential antineoplastic activity.
Host
Item no.
Amount 1 g
Available
PNU159682 Login PNU159682
Type Chemicals
Clone
Specific against Other
Appl. PNU-159682 is a major bioactive metabolite of Nemorubicin in human liver microsomes; > 3, 000-fold cytotoxic than its parent compound(MMDX and doxorubicin).
Host
Item no.
Amount 100 mg
Available
DTP3 Login DTP3
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 100 mg
Available
DTP3 Login DTP3
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 250 mg
Available
DTP3 Login DTP3
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 1 g
Available
FRAX-­486 Login FRAX-486
Type Chemicals
Clone
Specific against Other
Appl. FRAX486 is a selective inhibitor of group I PAKs with IC50s of 8.25/39.5, /55.3 nM for PAK1/PAK2/PAK3 respectivelt; less potent for PAK4(IC50=779 nM).
Host
Item no.
Amount 100 mg
Available
FRAX-­486 Login FRAX-486
Type Chemicals
Clone
Specific against Other
Appl. FRAX486 is a selective inhibitor of group I PAKs with IC50s of 8.25/39.5, /55.3 nM for PAK1/PAK2/PAK3 respectivelt; less potent for PAK4(IC50=779 nM).
Host
Item no.
Amount 250 mg
Available
FRAX-­486 Login FRAX-486
Type Chemicals
Clone
Specific against Other
Appl. FRAX486 is a selective inhibitor of group I PAKs with IC50s of 8.25/39.5, /55.3 nM for PAK1/PAK2/PAK3 respectivelt; less potent for PAK4(IC50=779 nM).
Host
Item no.
Amount 1 g
Available
BRACO19 trihydrochloride Login BRACO19 trihydrochloride
Type Chemicals
Clone
Specific against Other
Appl. BRACO19 is a telomerase inhibitor that stabilizes G-quadruplexes, targeting telomeric G-quadruplexes, inducing DNA damage and cell-cycle arrest.
Host
Item no.
Amount 100 mg
Available
BRACO19 trihydrochloride Login BRACO19 trihydrochloride
Type Chemicals
Clone
Specific against Other
Appl. BRACO19 is a telomerase inhibitor that stabilizes G-quadruplexes, targeting telomeric G-quadruplexes, inducing DNA damage and cell-cycle arrest.
Host
Item no.
Amount 250 mg
Available
BRACO19 trihydrochloride Login BRACO19 trihydrochloride
Type Chemicals
Clone
Specific against Other
Appl. BRACO19 is a telomerase inhibitor that stabilizes G-quadruplexes, targeting telomeric G-quadruplexes, inducing DNA damage and cell-cycle arrest.
Host
Item no.
Amount 1 g
Available
GW-­6604 Login GW-6604
Type Chemicals
Clone
Specific against Other
Appl. GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity.
Host
Item no.
Amount 100 mg
Available
GW-­6604 Login GW-6604
Type Chemicals
Clone
Specific against Other
Appl. GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity.
Host
Item no.
Amount 250 mg
Available
GW-­6604 Login GW-6604
Type Chemicals
Clone
Specific against Other
Appl. GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity.
Host
Item no.
Amount 1 g
Available
Vicriviroc maleate(Sch-­417690) Login Vicriviroc maleate(Sch-417690)
Type Chemicals
Clone
Specific against Other
Appl. Vicriviroc Malate is a potent CKR-5 (CCR5) antagonist with IC50 of 0.91 nM.
Host
Item no.
Amount 100 mg
Available
Vicriviroc maleate(Sch-­417690) Login Vicriviroc maleate(Sch-417690)
Type Chemicals
Clone
Specific against Other
Appl. Vicriviroc Malate is a potent CKR-5 (CCR5) antagonist with IC50 of 0.91 nM.
Host
Item no.
Amount 250 mg
Available
TAK-­242 (Resatorvid) Login TAK-242 (Resatorvid)
Type Inhibitors
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
OF-­C4-­Deg-­Lin Login OF-C4-Deg-Lin
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 50 mg
Available

1437732 Item(s)

per page

Page:
  1. 17
  2. 18
  3. 19
  4. 20
  5. 21
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