6336-34-1
6336-34-1 structure
- Name: OUL 35
- Chemical Name: 4-(4-carbamoylphenoxy)benzamide
- CAS Number: 6336-34-1
- Molecular Formula: C14H12N2O3
- Molecular Weight: 256.25700
- Catalog: Signaling Pathways Cell Cycle/DNA Damage PARP
- Create Date: 2017-02-17 19:36:55
- Modify Date: 2026-07-01 15:42:45
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OUL35 (NSC39047) is a potent and selective inhibitor of ARTD10 (PARP-10), with an IC50 of 329 nM[1].
| Name | 4-(4-carbamoylphenoxy)benzamide |
|---|---|
| Synonyms |
OUL35 >= (HPLC)
4,4'-oxy-di-benzoic acid diamide 4,4'-Oxydibenzamide , OUL35 OUL35, 10 mM in DMSO 4,4'-Oxydibenzamide Benzamide, 4,4'-oxybis 4,4'-oxydibenzamide NSC39047 4,4'-Oxybis[benzamide] TD10,PP,inhibit,DNA,OUL 35,NSC 39047,apoptosis,NSC-39047,PP10,poly ADP ribose polymerase,damage,HeLa,OUL35,Inhibitor,OUL-35 4.4'-Oxy-bis-benzamid 4,4'-Oxy-di-benzoesaeure-diamid 4-(4-cbamoylphenoxy)benzamide |
| Description | OUL35 (NSC39047) is a potent and selective inhibitor of ARTD10 (PARP-10), with an IC50 of 329 nM[1]. |
|---|---|
| Related Catalog | |
| Target |
ARTD10/PARP10:329 nM (IC50) |
| In Vitro | OUL35 rescues HeLa cells from ARTD10-induced cell death and sensitizes cells to DNA damage. OUL35 (3 μM) binds to endogenous ARTD10 in U2OS cells[1]. OUL35 also inhibits ARTD8 (23.4 μM), ARTD4 (22.6 μM), and ARTD15 (4.17 μM) but with modest potency[1]. OUL35 makes hydrogen bonds to the amide and carbonyl of Gly888 and to the side-chain hydroxyl of Ser927. OUL35 stacks between Tyr919 and Tyr932, like 3AB in the crystal structure[1]. |
| References |
| Density | 1.298g/cm3 |
|---|---|
| Boiling Point | 488.8ºC at 760 mmHg |
| Molecular Formula | C14H12N2O3 |
| Molecular Weight | 256.25700 |
| Flash Point | 257.9ºC |
| Exact Mass | 256.08500 |
| PSA | 95.41000 |
| LogP | 3.07730 |
| Index of Refraction | 1.633 |
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6336-34-1 |
| Literature: Eblinger, Frank; Schneider, Hans-Joerg Chemical Communications, 1998 , # 21 p. 2297 - 2298 |
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6336-34-1 |
| Literature: Eblinger, Frank; Schneider, Hans-Joerg Chemical Communications, 1998 , # 21 p. 2297 - 2298 |
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6336-34-1 |
| Literature: Hopff; Ohlinger Angewandte Chemie, 1949 , vol. 61, p. 183 Chem.Abstr., 1949 , p. 6183 |
