1. Immunology/Inflammation
  2. Cyclophilin
  3. CypD-IN-7

CypD-IN-7 is a potent cyclophilin D (CypD/PPIF) inhibitor that inhibits CypD PPIase activity (Ki = 2.4 nM) and provides protection against mitochondrial permeability transition pore (MPTP) opening. CypD-IN-7 can be used for pancreatitis research.

For research use only. We do not sell to patients.

CypD-IN-7

CypD-IN-7 Chemical Structure

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Description

CypD-IN-7 is a potent cyclophilin D (CypD/PPIF) inhibitor that inhibits CypD PPIase activity (Ki = 2.4 nM) and provides protection against mitochondrial permeability transition pore (MPTP) opening. CypD-IN-7 can be used for pancreatitis research[1].

IC50 & Target1

Cyclophilin D

2.4 nM (Ki)

In Vitro

CypD-IN-7 (18f) (39 nM-5 μM) increases mitochondrial calcium retention capacity (CRC) in isolated mouse liver mitochondria[1].
CypD-IN-7 (10 μM) markedly increases mitochondrial calcium retention capacity (CRC), and provides significantly superior protection against MPTP opening versus cyclosporin A (CsA) at 300 nM[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Parmacokinetics
Species Dose Route Tmax Cmax T1/2 AUClast AUCinf
Mice[1] 20 mg/kg i.p. 2.00 h 1633 ng/mL 3.70 h 8860 ng·h/mL 8940 ng·h/mL
In Vivo

CypD-IN-7 (18f) (50 mg/kg; i.p.; dosed immediately after the 3rd and 6th Caerulein (HY-A0190) injections and 2 h after the 7th injection) significantly reduces serum amylase, pancreatic MPO activity, edema/inflammation scores, and total histology score in a caerulein-induced acute pancreatitis (CER-AP) mouse model, whereas 20 mg/kg shows no significant effect[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Wild-type C57BL6/J male and female mice (10-12 weeks old); CER-AP induced by 7 hourly i.p. injections of caerulein (50 μg/kg)1
Dosage: 20 mg/kg; 50 mg/kg
Administration: i.p.; administered immediately after the 3rd and 6th Caerulein injections and 2 h after the 7th injection (end of the 2nd, 5th, and 8th hour of the experiment).
Result: 50 mg/kg (three doses) significantly reduced CER-elevated serum amylase, pancreatic MPO activity, and overall histology score; trypsin also showed a marked reduction, while 20 mg/kg showed no significant effect.
Molecular Weight

755.28

Formula

C41H44ClFN6O5

SMILES

FC1=CC=C(C(N2CCCN2C([C@@H](NC(NCC3=CC4=C(N[C@H]5[C@H](O)CO[C@@H]4C5)C=C3)=O)C6=CC=C(C7=CC=C(CN8CCOCC8)C=C7)C=C6)=O)=C1)Cl

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
CypD-IN-7
Cat. No.:
HY-179417
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