1. Immunology/Inflammation
  2. Complement System
  3. JPE-1375

JPE-1375 is a complement C5a receptor 1 (C5aR1) antagonist. JPE-1375 effectively inhibits polymorphonuclear leukocyte mobilization (EC50=6.9 μM) and reduces TNF levels (EC50=4.5 μM) in mice. JPE-1375 can be used in studies of autoimmune and inflammatory diseases.

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JPE-1375

JPE-1375 화학구조

CAS No. : 1254036-23-1

사이즈 가격 재고 수량
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
해외재고보유
Solution
10 mM * 1 mL in DMSO 해외재고보유
Solid
5 mg 해외재고보유
10 mg 해외재고보유
25 mg 해외재고보유
50 mg 해외재고보유
100 mg 해외재고보유
200 mg   견적 받기  
500 mg   견적 받기  

* 장바구니에 담기 전 물품의 수량을 선택해 주십시오.

This product is a controlled substance and not for sale in your territory.

고객리뷰

Based on 4 publication(s) in Google Scholar

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  • Biological Activity

  • 순도&문서

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  • 고객리뷰

제품 설명

JPE-1375 is a complement C5a receptor 1 (C5aR1) antagonist. JPE-1375 effectively inhibits polymorphonuclear leukocyte mobilization (EC50=6.9 μM) and reduces TNF levels (EC50=4.5 μM) in mice. JPE-1375 can be used in studies of autoimmune and inflammatory diseases[1].

IC50 & Target

C5aR1[1].

In Vivo

JPE-1375 (0.3, 1.0, 3.0 mg/kg; i.v.; single) inhibits PMN (polymorphonuclear leukocytes) mobilization and TNF with EC50 values of 6.9 and 4.5 μM, respectively[1].
JPE-1375 (1 mg/kg; i.v.; single) demonstrates a rapid distribution in the plasma, followed by elimination in mice[1].
JPE-1375 (1 mg/kg; i.v.; single) shows a strong negative correlation between PMN mobilization and TNF production with plasma concentrations[1].

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

Animal Model: C57BL/6J wild-type (10 to 12-week-old; C5a pharmacodynamic model)[1].
Dosage: 0.3, 1.0, 3.0 mg/kg
Administration: Intravenous injection; single.
Result: Significantly decreased C5a-mediated PMN mobilization at 1 and 3 mg/kg doses, while no effect was observed at a 0.3 mg/kg dose.
Showed a significant reduction in TNF plasma levels at 1 and 3 mg/kg dose with both compounds reducing C5a-mediated TNF by about 90%.
Animal Model: C57BL/6J wild-type mice(10 to 12-week-old)[1].
Dosage: 1 mg/kg
Administration: Intravenous injection; single.
Result: 1.19 Pharmacokinetic Parameters of JPE-1375 in C57BL/6J wild-type mice[1].
IV (1 mg/kg)
T1/2 (h) 0.13
Cmax (µg/mL) 7.18
AUC0-t (μg/mL•h) 2.40
AUC0-inf, obs (μg/mL•h) 2.41
AUC0-t/0-inf, obs (μg/mL•h) 1.00
AUMC0-inf, obs (μg/mL•h2) 0.13
MRT0-inf, obs (h) 0.05
Vz, obs ((μg)/(μg/mL)) 2.38
CL, obs ((μg)/(μg/mL)/h) 12.47
Vss, obs ((μg)/(μg/mL)) 0.66
분자량

955.08

화학식

C49H63FN10O9

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=C([C@@H]1CC(NC(N1)=O)=O)N[C@@H](CC2=CC=CC=C2)C(N[C@@H](CCCN)C(N3[C@@H](CCC3)C(N[C@@H](CCC(C)C)C(N[C@H](C(N[C@H](C(N)=O)CC4=CC=CC=C4)=O)CC5=CC=C(C=C5)F)=O)=O)=O)=O

선적

Room temperature in continental US; may vary elsewhere.

보관

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

용액&용해도
In Vitro: 

DMSO : 100 mg/mL (104.70 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.0470 mL 5.2352 mL 10.4703 mL
5 mM 0.2094 mL 1.0470 mL 2.0941 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • 몰농도 계산기

  • 농도 희석 계산기

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
순도&문서

Purity: 99.96%

References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.0470 mL 5.2352 mL 10.4703 mL 26.1758 mL
5 mM 0.2094 mL 1.0470 mL 2.0941 mL 5.2352 mL
10 mM 0.1047 mL 0.5235 mL 1.0470 mL 2.6176 mL
15 mM 0.0698 mL 0.3490 mL 0.6980 mL 1.7451 mL
20 mM 0.0524 mL 0.2618 mL 0.5235 mL 1.3088 mL
25 mM 0.0419 mL 0.2094 mL 0.4188 mL 1.0470 mL
30 mM 0.0349 mL 0.1745 mL 0.3490 mL 0.8725 mL
40 mM 0.0262 mL 0.1309 mL 0.2618 mL 0.6544 mL
50 mM 0.0209 mL 0.1047 mL 0.2094 mL 0.5235 mL
60 mM 0.0175 mL 0.0873 mL 0.1745 mL 0.4363 mL
80 mM 0.0131 mL 0.0654 mL 0.1309 mL 0.3272 mL
100 mM 0.0105 mL 0.0524 mL 0.1047 mL 0.2618 mL
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Inquiry Information

상품명:
JPE-1375
Cat. No.:
HY-148141
수량:
MCE Japan Authorized Agent: