NBI 30545
NBI 30545 is a blood-brain barrier permeable CRF1R antagonist with a Ki value of 3.4 nM for the human receptor. NBI 30545 inhibits CRF-stimulated intracellular cAMP accumulation and ACTH release. NBI 30545 can be used in the research of depression, anxiety disorders and stress-related diseases.
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- CAS No.: 195054-99-0
- 화학식: C22H30N4O3
- 분자량:398.51
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
제품 설명
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| CHO | IC50 |
76 nM
Compound: 8
|
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
|
[PMID: 15341493] |
| Pituitary gland cell | IC50 |
37 nM
Compound: 18n
|
Inhibition of CRF-stimulated ACTH release in cultured rat anterior pituitary cells
Inhibition of CRF-stimulated ACTH release in cultured rat anterior pituitary cells
|
[PMID: 15203140] |
| Pituitary gland cell | IC50 |
76 nM
Compound: 18n
|
Inhibition of CRF-stimulated cAMP production in cultured rat anterior pituitary cells
Inhibition of CRF-stimulated cAMP production in cultured rat anterior pituitary cells
|
[PMID: 15203140] |
In Vitro
NBI 30545 inhibits CRF-stimulated cAMP accumulation in cells expressing the human CRF1 receptor with an IC50 of 76 nM[1].
NBI 30545 inhibits CRF-stimulated ACTH release in cultured rat anterior pituitary cells with an IC50 of 37 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. .
Parmacokinetics
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sprague-Dawley[1]
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Dosage:10 mg/kg (i.v.); 10 mg/kg (p.o.)
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Administration:i.v.; single dose; p.o.; single dose
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Result:Achieved a volume of distribution of 4.7 L/kg, clearance of 43 mL/min/kg, and a half-life of 1.1 h after intravenous administration.
Reached a plasma AUC of 1182 ng/mL·h, brain AUC of 1472 ng/g·h, oral bioavailability of 30.5%, and a brain/plasma ratio of 1.2 after oral administration.
Chemical Information
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CAS No. 195054-99-0
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분자량 398.51
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화학식 C22H30N4O3
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SMILES
N1=C(C=C(N2N=C(C(=C12)C=3C=CC(OC)=CC3OC)C)N(CCOC)CCC)C
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)