Angiogenesis
Research Areas
Products Related to Angiogenesis(378)
- GC43514D-myo-Inositol-1,3,4,5,6-pentaphosphate (ammonium salt)Purity: >98.00%
Inositol-1,3,4,5,6-pentaphosphate (Ins(1,3,4,5,6)P5) is one of the many inositol phosphate isomers that act as small, soluble second messengers in the transmission of cellular signals.
- GC43515D-myo-Inositol-1,3,4,5,6-pentaphosphate (sodium salt)Purity: >98.00%
The phosphatidylinositol 3-kinase (PI3K)/Akt signal transduction pathway plays critical roles in cell growth and proliferation making it an attractive target for anticancer agents.
- GC43727Ganglioside GD1a mixture (sodium salt)CAS: 12707-58-3Purity: >98.00%
Ganglioside GD1a is a sialic acid-containing glycosphingolipid found in brain, erythrocytes, bone marrow, testis, spleen, and liver.
- GC43732Ganglioside GM3 Mixture (sodium salt)CAS: 54827-14-4Purity: >98.00%
Ganglioside GM3 is a monosialoganglioside that demonstrates antiproliferative and proapoptotic effects in tumor cells by modulating cell adhesion, proliferation, and differentiation.
- GC43803HA-1077 (hydrochloride)CAS: 203911-27-7Purity: >98.00%
Fasudil (HA-1077; AT877) dihydrochloride is a nonspecific RhoA/ROCK inhibitor and also has inhibitory effect on protein kinases, with an Ki of 0.33 μM for ROCK1, IC50s of 0.158 μM and 4.58 μM, 12.30 μ ;M, 1.650 μM fÜr ROCK2 bzw. PKA, PKC, PKG. HA-1077 (Hydrochlorid) ist auch ein potenter Ca2+-Kanalantagonist und Vasodilatator.
- GC44290NAADP (sodium salt)Purity: >95.00%
Nicotinic acid adenine dinucleotide phosphate (NAADP) is a secondary messenger that induces calcium mobilization.
- GC44358Nebivolol O-β-D-GlucuronidePurity: >95.00%
Nebivolol O-β-D-glucuronide is an active metabolite of the β1-adrenergic receptor antagonist nebivolol.
- GC44465NSC 12CAS: 102586-30-1Purity: >98.00%
NSC 12 ist eine extrazellulÄre Falle des Fibroblasten-Wachstumsfaktors 2 (FGF2), der FGF2 bindet und seine Wechselwirkung mit FGFR1 stÖrt. NSC 12 hemmt die Proliferation verschiedener FGF-abhÄngiger Tumorzellen sowohl in vitro als auch in vivo ohne systemische toxische Wirkungen.
- GC44475NVP-BEZ235 (hydrochloride)CAS: 2319647-83-9Purity: >98.00%
NVP-BEZ235 is a potent dual inhibitor of phosphatidylinositol 3-kinase (PI3K) and mTOR that is well tolerated, displays disease stasis when administered orally, and enhances the efficacy of other anticancer agents when used in in vivo combination studies.
- GC44584PD 168368CAS: 204066-82-0Purity: >95.00%
PD 168368 ist ein potenter, kompetitiver und selektiver Neuromedin-B-Rezeptor (NMB-R)-Antagonist mit einem Ki von 15-45 nM. PD 168368 ist ein Antagonist des Neuromedin-B-Rezeptors (NMBR; IC50=96 nM)/Gastrin-Releasing-Peptid-Rezeptors (GRPR IC50=3500 nM). PD 168368 ist auch ein gemischter FPR1/FPR2/FPR3-Agonist mit EC50-Werten von 0,57, 0,24 bzw. 2,7 nM.
- GC44956StreptochlorinCAS: 120191-51-7Purity: >98.00%
Streptochlorin is a bacterial metabolite originally isolated from Streptomyces sp.
- GC44966Sucrose octasulfate (potassium salt)CAS: 73264-44-5Purity: >95.00%
Sucrose octasulfate (SOS), a component of the gastrointestinal protectant sucralfate, is an alkaline aluminum-sucrose complex that inhibits peptic hydrolysis and raises gastric pH, protecting esophageal epithelium against acid injury.
- GC45054Tie2 Inhibitor 7CAS: 1020412-97-8Purity: >95.00%
Tie2 Inhibitor 7 blocks Tie2 kinase activity with a Ki value of 1.3 μM..
- GC45269(±)10(11)-DiHDPACAS: 1345275-22-0Purity: >98.00%
(±)10(11)-DiHDPA is produced from cytochrome P450 epoxygenase action on docosahexaenoic acid.
- GC45677Anlotinib (hydrochloride)CAS: 1058157-76-8Purity: >98.00%
A neuropeptide with diverse biological activities
- GC45767Dovitinib-d8CAS: 1246819-84-0Purity: >99.00%
Dovitinib-D8 (CHIR-258-D8) ist das mit Deuterium bezeichnete Dovitinib. Dovitinib (CHIR-258) ist ein Multi-Targeting-Tyrosinkinase-Inhibitor mit IC50-Werten von 1, 2, 8/9, 10/13/8, 27/210 nM fÜr FLT3, c-Kit, FGFR1/FGFR3, VEGFR1/VEGFR2/ VEGFR3 bzw. PDGFRα/PDGFRβ.
- GC45769Vandetanib-d6CAS: 1174683-49-8Purity: >99.00%
Vandetanib-d6 (ZD6474-d6) ist das als Vandetanib bezeichnete Deuterium. Vandetanib (D6474) ist ein potenter, oral aktiver Inhibitor der VEGFR2/KDR-Tyrosinkinase-AktivitÄt (IC50=40 nM). Vandetanib hat auch AktivitÄt gegenÜber der Tyrosinkinase-AktivitÄt von VEGFR3/FLT4 (IC50 = 110 nM) und EGFR/HER1 (IC50 = 500 nM).
- GC45798Rhein-13C4CAS: 1189928-10-6Purity: >95.00%
An internal standard for the quantification of rhein
- GC45880Cimetidine-d3CAS: 1185237-29-9Purity: >99.00%
An internal standard for the quantification of cimetidine
- GC45922(±)11(12)-EET-d11 methyl esterPurity: >99.00%
A neuropeptide with diverse biological activities
- GC46304(±)-Nebivolol-d4 (hydrochloride)CAS: 2701283-32-9Purity: >99.00%
A neuropeptide with diverse biological activities
- GC4647418-DeoxyherboxidieneCAS: 1200128-66-0Purity: >70.00%
18-Desoxyherboxidien (RQN-18690A) ist ein potenter Angiogenese-Inhibitor.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC43514 | D-myo-Inositol-1,3,4,5,6-pentaphosphate (ammonium salt) | - | >98.00% | |
Inositol-1,3,4,5,6-pentaphosphate (Ins(1,3,4,5,6)P5) is one of the many inositol phosphate isomers that act as small, soluble second messengers in the transmission of cellular signals. | ||||
| GC43515 | D-myo-Inositol-1,3,4,5,6-pentaphosphate (sodium salt) | - | >98.00% | |
The phosphatidylinositol 3-kinase (PI3K)/Akt signal transduction pathway plays critical roles in cell growth and proliferation making it an attractive target for anticancer agents. | ||||
| GC43727 | Ganglioside GD1a mixture (sodium salt) | 12707-58-3 | >98.00% | |
Ganglioside GD1a is a sialic acid-containing glycosphingolipid found in brain, erythrocytes, bone marrow, testis, spleen, and liver. | ||||
| GC43732 | Ganglioside GM3 Mixture (sodium salt) | 54827-14-4 | >98.00% | |
Ganglioside GM3 is a monosialoganglioside that demonstrates antiproliferative and proapoptotic effects in tumor cells by modulating cell adhesion, proliferation, and differentiation. | ||||
| GC43803 | HA-1077 (hydrochloride) | 203911-27-7 | >98.00% | |
Fasudil (HA-1077; AT877) dihydrochloride is a nonspecific RhoA/ROCK inhibitor and also has inhibitory effect on protein kinases, with an Ki of 0.33 μM for ROCK1, IC50s of 0.158 μM and 4.58 μM, 12.30 μ ;M, 1.650 μM fÜr ROCK2 bzw. PKA, PKC, PKG. HA-1077 (Hydrochlorid) ist auch ein potenter Ca2+-Kanalantagonist und Vasodilatator. | ||||
| GC44290 | NAADP (sodium salt) | - | >95.00% | |
Nicotinic acid adenine dinucleotide phosphate (NAADP) is a secondary messenger that induces calcium mobilization. | ||||
| GC44358 | Nebivolol O-β-D-Glucuronide | - | >95.00% | |
Nebivolol O-β-D-glucuronide is an active metabolite of the β1-adrenergic receptor antagonist nebivolol. | ||||
| GC44465 | NSC 12 | 102586-30-1 | >98.00% | |
NSC 12 ist eine extrazellulÄre Falle des Fibroblasten-Wachstumsfaktors 2 (FGF2), der FGF2 bindet und seine Wechselwirkung mit FGFR1 stÖrt. NSC 12 hemmt die Proliferation verschiedener FGF-abhÄngiger Tumorzellen sowohl in vitro als auch in vivo ohne systemische toxische Wirkungen. | ||||
| GC44475 | NVP-BEZ235 (hydrochloride) | 2319647-83-9 | >98.00% | |
NVP-BEZ235 is a potent dual inhibitor of phosphatidylinositol 3-kinase (PI3K) and mTOR that is well tolerated, displays disease stasis when administered orally, and enhances the efficacy of other anticancer agents when used in in vivo combination studies. | ||||
| GC44584 | PD 168368 | 204066-82-0 | >95.00% | |
PD 168368 ist ein potenter, kompetitiver und selektiver Neuromedin-B-Rezeptor (NMB-R)-Antagonist mit einem Ki von 15-45 nM. PD 168368 ist ein Antagonist des Neuromedin-B-Rezeptors (NMBR; IC50=96 nM)/Gastrin-Releasing-Peptid-Rezeptors (GRPR IC50=3500 nM). PD 168368 ist auch ein gemischter FPR1/FPR2/FPR3-Agonist mit EC50-Werten von 0,57, 0,24 bzw. 2,7 nM. | ||||
| GC44800 | Quininib | 143816-42-6 | >98% | |
A CysLT 1 and CysLT 2 receptor antagonist | ||||
| GC44956 | Streptochlorin | 120191-51-7 | >98.00% | |
Streptochlorin is a bacterial metabolite originally isolated from Streptomyces sp. | ||||
| GC44966 | Sucrose octasulfate (potassium salt) | 73264-44-5 | >95.00% | |
Sucrose octasulfate (SOS), a component of the gastrointestinal protectant sucralfate, is an alkaline aluminum-sucrose complex that inhibits peptic hydrolysis and raises gastric pH, protecting esophageal epithelium against acid injury. | ||||
| GC45054 | Tie2 Inhibitor 7 | 1020412-97-8 | >95.00% | |
Tie2 Inhibitor 7 blocks Tie2 kinase activity with a Ki value of 1.3 μM.. | ||||
| GC45269 | (±)10(11)-DiHDPA | 1345275-22-0 | >98.00% | |
(±)10(11)-DiHDPA is produced from cytochrome P450 epoxygenase action on docosahexaenoic acid. | ||||
| GC45677 | Anlotinib (hydrochloride) | 1058157-76-8 | >98.00% | |
A neuropeptide with diverse biological activities | ||||
| GC45688 | STX140 | 401600-86-0 | >98.00% | |
An estrogen sulfamate | ||||
| GC45767 | Dovitinib-d8 | 1246819-84-0 | >99.00% | |
Dovitinib-D8 (CHIR-258-D8) ist das mit Deuterium bezeichnete Dovitinib. Dovitinib (CHIR-258) ist ein Multi-Targeting-Tyrosinkinase-Inhibitor mit IC50-Werten von 1, 2, 8/9, 10/13/8, 27/210 nM fÜr FLT3, c-Kit, FGFR1/FGFR3, VEGFR1/VEGFR2/ VEGFR3 bzw. PDGFRα/PDGFRβ. | ||||
| GC45769 | Vandetanib-d6 | 1174683-49-8 | >99.00% | |
Vandetanib-d6 (ZD6474-d6) ist das als Vandetanib bezeichnete Deuterium. Vandetanib (D6474) ist ein potenter, oral aktiver Inhibitor der VEGFR2/KDR-Tyrosinkinase-AktivitÄt (IC50=40 nM). Vandetanib hat auch AktivitÄt gegenÜber der Tyrosinkinase-AktivitÄt von VEGFR3/FLT4 (IC50 = 110 nM) und EGFR/HER1 (IC50 = 500 nM). | ||||
| GC45798 | Rhein-13C4 | 1189928-10-6 | >95.00% | |
An internal standard for the quantification of rhein | ||||
| GC45880 | Cimetidine-d3 | 1185237-29-9 | >99.00% | |
An internal standard for the quantification of cimetidine | ||||
| GC45922 | (±)11(12)-EET-d11 methyl ester | - | >99.00% | |
A neuropeptide with diverse biological activities | ||||
| GC46304 | (±)-Nebivolol-d4 (hydrochloride) | 2701283-32-9 | >99.00% | |
A neuropeptide with diverse biological activities | ||||
| GC46474 | 18-Deoxyherboxidiene | 1200128-66-0 | >70.00% | |
18-Desoxyherboxidien (RQN-18690A) ist ein potenter Angiogenese-Inhibitor. | ||||
