English
 
My Account  

REGISTER & SECURE BENEFITS

  • View prices & discounts
  • Free gifts
  • Request & accept offers online
LOGIN NOW Not yet registered? Create your free account here!
Comparison
Results

Filter Results

Typ
Specific against
Host
Clone
Applications
Isotype
Manufacturer

Molecules

1437732 Item(s)

per page

Page:
  1. 11
  2. 12
  3. 13
  4. 14
  5. 15
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
Mavatrep(JNJ-­39439335) Chemicals Other Mavatrep is an orally bioavailable TRPV1 antagonist (Ki=6.5 nM), exhibits minimal effect on the enzymatic activity (IC50 > 25 μM) of CYP isoforms 3A4, 1A2, and 2D6. DCC-DC8378-1g

DCChemicals 		1 g Login
Compare
PF-­5006739 Chemicals Other PF-5006739 is a potent inhibitor of casein kinases 1 delta (CK1δ) and 1 epsilon (CK1ε) DCC-DC8146-100mg

DCChemicals 		100 mg Login
Compare
PF-­5006739 Chemicals Other PF-5006739 is a potent inhibitor of casein kinases 1 delta (CK1δ) and 1 epsilon (CK1ε) DCC-DC8146-250mg

DCChemicals 		250 mg Login
Compare
PF-­5006739 Chemicals Other PF-5006739 is a potent inhibitor of casein kinases 1 delta (CK1δ) and 1 epsilon (CK1ε) DCC-DC8146-1g

DCChemicals 		1 g Login
Compare
LY311727 Chemicals Other PLA DCC-DC8602-100mg

DCChemicals 		100 mg Login
Compare
LY311727 Chemicals Other PLA DCC-DC8602-250mg

DCChemicals 		250 mg Login
Compare
LY311727 Chemicals Other PLA DCC-DC8602-1g

DCChemicals 		1 g Login
Compare
Tradipitant(VLY-­686) Chemicals Other IV DCC-DC8176-100mg

DCChemicals 		100 mg Login
Compare
Tradipitant(VLY-­686) Chemicals Other IV DCC-DC8176-250mg

DCChemicals 		250 mg Login
Compare
Tradipitant(VLY-­686) Chemicals Other IV DCC-DC8176-1g

DCChemicals 		1 g Login
Compare
SR 49059 Chemicals Other Potent and selective non-peptide vasopressin V1A receptor antagonist; devoid of agonist activity. Displays high affinity and efficacy at both rat (KI=1.6 nM) and human (KI -1.1 - 6.3 nM) V1A receptors. DCC-DC8603-100mg

DCChemicals 		100 mg Login
Compare
SR 49059 Chemicals Other Potent and selective non-peptide vasopressin V1A receptor antagonist; devoid of agonist activity. Displays high affinity and efficacy at both rat (KI=1.6 nM) and human (KI -1.1 - 6.3 nM) V1A receptors. DCC-DC8603-250mg

DCChemicals 		250 mg Login
Compare
SR 49059 Chemicals Other Potent and selective non-peptide vasopressin V1A receptor antagonist; devoid of agonist activity. Displays high affinity and efficacy at both rat (KI=1.6 nM) and human (KI -1.1 - 6.3 nM) V1A receptors. DCC-DC8603-1g

DCChemicals 		1 g Login
Compare
KW-­2478 Chemicals Other KW-2478 is a nonansamycin HSP90 inhibitor with IC50 of 3.8 nM. Phase 1/2 DCC-DC7449-100mg

DCChemicals 		100 mg Login
Compare
KW-­2478 Chemicals Other KW-2478 is a nonansamycin HSP90 inhibitor with IC50 of 3.8 nM. Phase 1/2 DCC-DC7449-250mg

DCChemicals 		250 mg Login
Compare
KW-­2478 Chemicals Other KW-2478 is a nonansamycin HSP90 inhibitor with IC50 of 3.8 nM. Phase 1/2 DCC-DC7449-1g

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

DCChemicals 		1 g Login
Compare
GO 6976 Chemicals Other Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat brain), PKCα, and PKCβ1, respectively. Also a potent inhibitor of JAK2 and Flt3. DCC-DC7421-250mg

DCChemicals 		250 mg Login
Compare
GO 6976 Chemicals Other Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat brain), PKCα, and PKCβ1, respectively. Also a potent inhibitor of JAK2 and Flt3. DCC-DC7421-1g

DCChemicals 		1 g Login
Compare
GO 6976 Chemicals Other Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat brain), PKCα, and PKCβ1, respectively. Also a potent inhibitor of JAK2 and Flt3. DCC-DC7421-100mg

DCChemicals 		100 mg Login
Compare
Givinostat (ITF2357) Chemicals Other other DCC-DC7432-100mg

DCChemicals 		100 mg Login
Compare
Givinostat (ITF2357) Chemicals Other other DCC-DC7432-250mg

DCChemicals 		250 mg Login
Compare
Givinostat (ITF2357) Chemicals Other other DCC-DC7432-1g

DCChemicals 		1 g Login
Compare
Ginsenoside Rg1 Chemicals Other other DCC-DCR-015-1g

DCChemicals 		1 g Login
Compare
Ginsenoside Rb1 Chemicals Other DCC-DCR-012-1g

DCChemicals 		1 g Login
Compare
Name Price
Mavatrep(JNJ-­39439335) Login Mavatrep(JNJ-39439335)
Type Chemicals
Clone
Specific against Other
Appl. Mavatrep is an orally bioavailable TRPV1 antagonist (Ki=6.5 nM), exhibits minimal effect on the enzymatic activity (IC50 > 25 μM) of CYP isoforms 3A4, 1A2, and 2D6.
Host
Item no.
Amount 1 g
Available
PF-­5006739 Login PF-5006739
Type Chemicals
Clone
Specific against Other
Appl. PF-5006739 is a potent inhibitor of casein kinases 1 delta (CK1δ) and 1 epsilon (CK1ε)
Host
Item no.
Amount 100 mg
Available
PF-­5006739 Login PF-5006739
Type Chemicals
Clone
Specific against Other
Appl. PF-5006739 is a potent inhibitor of casein kinases 1 delta (CK1δ) and 1 epsilon (CK1ε)
Host
Item no.
Amount 250 mg
Available
PF-­5006739 Login PF-5006739
Type Chemicals
Clone
Specific against Other
Appl. PF-5006739 is a potent inhibitor of casein kinases 1 delta (CK1δ) and 1 epsilon (CK1ε)
Host
Item no.
Amount 1 g
Available
LY311727 Login LY311727
Type Chemicals
Clone
Specific against Other
Appl. PLA
Host
Item no.
Amount 100 mg
Available
LY311727 Login LY311727
Type Chemicals
Clone
Specific against Other
Appl. PLA
Host
Item no.
Amount 250 mg
Available
LY311727 Login LY311727
Type Chemicals
Clone
Specific against Other
Appl. PLA
Host
Item no.
Amount 1 g
Available
Tradipitant(VLY-­686) Login Tradipitant(VLY-686)
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 100 mg
Available
Tradipitant(VLY-­686) Login Tradipitant(VLY-686)
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 250 mg
Available
Tradipitant(VLY-­686) Login Tradipitant(VLY-686)
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 1 g
Available
SR 49059 Login SR 49059
Type Chemicals
Clone
Specific against Other
Appl. Potent and selective non-peptide vasopressin V1A receptor antagonist; devoid of agonist activity. Displays high affinity and efficacy at both rat (KI=1.6 nM) and human (KI -1.1 - 6.3 nM) V1A receptors.
Host
Item no.
Amount 100 mg
Available
SR 49059 Login SR 49059
Type Chemicals
Clone
Specific against Other
Appl. Potent and selective non-peptide vasopressin V1A receptor antagonist; devoid of agonist activity. Displays high affinity and efficacy at both rat (KI=1.6 nM) and human (KI -1.1 - 6.3 nM) V1A receptors.
Host
Item no.
Amount 250 mg
Available
SR 49059 Login SR 49059
Type Chemicals
Clone
Specific against Other
Appl. Potent and selective non-peptide vasopressin V1A receptor antagonist; devoid of agonist activity. Displays high affinity and efficacy at both rat (KI=1.6 nM) and human (KI -1.1 - 6.3 nM) V1A receptors.
Host
Item no.
Amount 1 g
Available
KW-­2478 Login KW-2478
Type Chemicals
Clone
Specific against Other
Appl. KW-2478 is a nonansamycin HSP90 inhibitor with IC50 of 3.8 nM. Phase 1/2
Host
Item no.
Amount 100 mg
Available
KW-­2478 Login KW-2478
Type Chemicals
Clone
Specific against Other
Appl. KW-2478 is a nonansamycin HSP90 inhibitor with IC50 of 3.8 nM. Phase 1/2
Host
Item no.
Amount 250 mg
Available
KW-­2478 Login KW-2478
Type Chemicals
Clone
Specific against Other
Appl. KW-2478 is a nonansamycin HSP90 inhibitor with IC50 of 3.8 nM. Phase 1/2
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 1 g
Available
GO 6976 Login GO 6976
Type Chemicals
Clone
Specific against Other
Appl. Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat brain), PKCα, and PKCβ1, respectively. Also a potent inhibitor of JAK2 and Flt3.
Host
Item no.
Amount 250 mg
Available
GO 6976 Login GO 6976
Type Chemicals
Clone
Specific against Other
Appl. Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat brain), PKCα, and PKCβ1, respectively. Also a potent inhibitor of JAK2 and Flt3.
Host
Item no.
Amount 1 g
Available
GO 6976 Login GO 6976
Type Chemicals
Clone
Specific against Other
Appl. Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat brain), PKCα, and PKCβ1, respectively. Also a potent inhibitor of JAK2 and Flt3.
Host
Item no.
Amount 100 mg
Available
Givinostat (ITF2357) Login Givinostat (ITF2357)
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 100 mg
Available
Givinostat (ITF2357) Login Givinostat (ITF2357)
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 250 mg
Available
Givinostat (ITF2357) Login Givinostat (ITF2357)
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 1 g
Available
Ginsenoside Rg1 Login Ginsenoside Rg1
Type Chemicals
Clone
Specific against Other
Appl. other
Host
Item no.
Amount 1 g
Available
Ginsenoside Rb1 Login Ginsenoside Rb1
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available

1437732 Item(s)

per page

Page:
  1. 11
  2. 12
  3. 13
  4. 14
  5. 15
Contact

Hölzel Diagnostika Handels GmbH
Weinsbergstr 118a
50823 Cologne
Germany

T +49 221 126 02 66
F +49 221 126 02 67

info@hoelzel.de

About Hölzel
Service
Infodesk
Spendenaktion Datenschutzsiegel

Copyright 2025 Hölzel Diagnostika Handels GmbH

To top