Angiogenesis
Research Areas
Products Related to Angiogenesis(415)
- GC79140Cyclo(-RGDfK), 5/6 FAM labeled TFAPurity: >98.00%
Cyclo(-RGDfK), 5/6 FAM labeled TFA is a Cyclo(-RGDfK) TFA labeled with 5/6 FAM.
- GC79141T7 Peptide TFAPurity: >98.00%
T7 Peptide TFA is a protein synthesis inhibitor and anti-angiogenic agent, with a K d of 10 nM for human transferrin receptor.
- GC79669PHD-1-IN-4CAS: 2009343-19-3Purity: >99.50%
PHD-1-IN-4 is a brain-penetrant PHD-1 inhibitor with an IC 50 of 0.074 μM [1] .
- GC79816CryptolepineCAS: 480-26-2Purity: >98.00%
Cryptolepine is an orally active multi-potent alkaloid with anti-cancer, anti-bacterial, anti-viral, anti-malarial, anti-inflammatory, anti-hyperglycemic, relieve pain and other properties.
- GC79995(S,R)-EmvistegrastCAS: 2417307-56-1Purity: >98.00%
(S,R)-Emvistegrast ((S,R)-GS-1427) is an isomer of Emvistegrast.
- GC80856(R,R)-BexobrutidegCAS: 2649400-33-7Purity: >98.50%
(R,R)-Bexobrutideg is the (R,R)-enantiomer of Bexobrutideg.
- GC81027PROTAC HIF-1α degrader-2CAS: 3095636-64-6Purity: >98.00%
PROTAC HIF-1α degrader-2 is a highly efficient and selective PROTAC degrader targeting HIF-1α. PROTAC HIF-1α degrader-2 promotes HIF-1α degradation via the ubiquitin-proteasome pathway by facilitating the formation of a HIF-1α/VHL ternary complex.
- GC81297DFCI-002-06CAS: 3092208-36-8Purity: >98.00%
DFCI-002-06 is an orally active dual-target HCK/BTK PROTAC degrader with DC₅₀ values for HCK and BTK of 1.3 and 4.5 nM respectively.
- GC81556FZ1 peptidePurity: >99.50%
FZ1 peptide is a cyclic heptapeptide and also an integrin αvβ3 agonist.
- GC815842-Amino-2-deoxy-D-glucopyranoseCAS: 90-77-7Purity: >98.00%
2-Amino-2-deoxy-D-glucopyranose is an isomeric form of Glucosamine.
- GC81602Glucosamine sulfate potassium chlorideCAS: 1296149-08-0Purity: >98.00%
Glucosamine sulfate potassium chloride is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC79140 | Cyclo(-RGDfK), 5/6 FAM labeled TFA | - | >98.00% | |
Cyclo(-RGDfK), 5/6 FAM labeled TFA is a Cyclo(-RGDfK) TFA labeled with 5/6 FAM. | ||||
| GC79141 | T7 Peptide TFA | - | >98.00% | |
T7 Peptide TFA is a protein synthesis inhibitor and anti-angiogenic agent, with a K d of 10 nM for human transferrin receptor. | ||||
| GC79574 | mCPX | 1351572-56-9 | >98.00% | |
mCPX is a prodrug of the antifungal agent Ciclopirox olamine (CPX). | ||||
| GC79669 | PHD-1-IN-4 | 2009343-19-3 | >99.50% | |
PHD-1-IN-4 is a brain-penetrant PHD-1 inhibitor with an IC 50 of 0.074 μM [1] . | ||||
| GC79670 | ZG-2686 | 1795110-22-3 | >98.00% | |
ZG-2686 is a potent and selective HIF-2α agonist with an EC 50 of 0.25 µM. | ||||
| GC79671 | HIF-IN-2 | 1040535-05-4 | >95.00% | |
HIF-IN-2 is a HIF/HIF prolyl hydroxylase inhibitor. | ||||
| GC79816 | Cryptolepine | 480-26-2 | >98.00% | |
Cryptolepine is an orally active multi-potent alkaloid with anti-cancer, anti-bacterial, anti-viral, anti-malarial, anti-inflammatory, anti-hyperglycemic, relieve pain and other properties. | ||||
| GC79995 | (S,R)-Emvistegrast | 2417307-56-1 | >98.00% | |
(S,R)-Emvistegrast ((S,R)-GS-1427) is an isomer of Emvistegrast. | ||||
| GC80483 | IOX2-NH2 | 931400-77-0 | >98.00% | |
IOX2 -NH2 (example 115) is a derivative of IOX2. | ||||
| GC80856 | (R,R)-Bexobrutideg | 2649400-33-7 | >98.50% | |
(R,R)-Bexobrutideg is the (R,R)-enantiomer of Bexobrutideg. | ||||
| GC80928 | NP1192 | 2966791-41-1 | >99.00% | |
NP1192 is a potent, selective PROTAC NAT10 degrader. | ||||
| GC81027 | PROTAC HIF-1α degrader-2 | 3095636-64-6 | >98.00% | |
PROTAC HIF-1α degrader-2 is a highly efficient and selective PROTAC degrader targeting HIF-1α. PROTAC HIF-1α degrader-2 promotes HIF-1α degradation via the ubiquitin-proteasome pathway by facilitating the formation of a HIF-1α/VHL ternary complex. | ||||
| GC81031 | NEO-811 | 3084635-77-5 | >98.00% | |
NEO-811 is a selective and orally active ARNT (HIF-1β) molecular glue degrader. | ||||
| GC81297 | DFCI-002-06 | 3092208-36-8 | >98.00% | |
DFCI-002-06 is an orally active dual-target HCK/BTK PROTAC degrader with DC₅₀ values for HCK and BTK of 1.3 and 4.5 nM respectively. | ||||
| GC81350 | THR-123 TFA | - | >99.50% | |
THR-123 TFA is an orally active ALK3 peptide agonist. | ||||
| GC81447 | ALDOA-IN-1 | - | >98.00% | |
ALDOA-IN-1 is an aldolase A (ALDOA) inhibitor. | ||||
| GC81556 | FZ1 peptide | - | >99.50% | |
FZ1 peptide is a cyclic heptapeptide and also an integrin αvβ3 agonist. | ||||
| GC81584 | 2-Amino-2-deoxy-D-glucopyranose | 90-77-7 | >98.00% | |
2-Amino-2-deoxy-D-glucopyranose is an isomeric form of Glucosamine. | ||||
| GC81595 | BCS12 | 329719-71-3 | >99.50% | |
BCS12 is a CAIX inhibitor. | ||||
| GC81602 | Glucosamine sulfate potassium chloride | 1296149-08-0 | >98.00% | |
Glucosamine sulfate potassium chloride is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement. | ||||
| GC81639 | SH-26 | - | >98.00% | |
SH-26 is a PHD1 PROTAC degrader with DC 50 s of 1.06 μM, 4.16 μM and 4.91 μM in MDA-MB-231, HepG2 and HEK-293T cells, respectively. | ||||
| GC81830 | D-RGDW acetate | - | >98.00% | |
D-RGDW acetate is an Arg-Gly-Asp (RGD) containing peptide. | ||||
| GC90787 | Lipid A4 | 2639634-71-0 | >95.00% | |
Ein verzweigter ionisierbarer kationischer Lipidoid. | ||||
| GC91360 | NM-3 | 181427-78-1 | >98.00% | |
NM-3 ist ein synthetisches Isocumarin und ein Inhibitor der Angiogenese. | ||||