Cat. No.: HY-132191

Pradimicin A

Pradimicin A is a potent antifungal agent with a minimum inhibitory concentration (MIC) of 4 μg/mL against Candida rugosa. Pradimicin A exhibits antiviral activity against SARS-CoV, human immunodeficiency virus (HIV) and other enveloped viruses. Pradimicin A exerts its fungicidal activity through a Ca²⁺-dependent mechanism, which induces fungal lysis. Pradimicin A can be used in research related to fungal infections, HIV infections and COVID-19.

연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.

CAS No.: 117704-65-1
화학식: C₄₀H₄₄N₂O₁₈
분자량:840.78

보관:

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

Data Sheet (277 KB)

Pradimicin A Chemical Structure

CAS No.: 117704-65-1

Amount: USD 0.00

* 장바구니에 담기 전 물품의 수량을 선택해 주십시오.

Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- 제품 설명
- IC₅₀ & Target
- Cellular Effect
- In Vitro
Chemical Information
순도&문서
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

제품 설명

IC₅₀ & Target

^[1]

HIV

All HIV Isoforms :

Cellular Effect

Cell Line	Type	Value	Description	References
C8166	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human C8166 cells after 3 to 4 days Cytotoxicity against human C8166 cells after 3 to 4 days	[PMID: 20047920]
C8166	EC₅₀	2.6 μM Compound: PRM-A	Antiviral activity against HIV-1 3B infected in human C8166 cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis Antiviral activity against HIV-1 3B infected in human C8166 cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis	[PMID: 20047920]
Caco-2	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human Caco2 cells after 3 to 4 days Cytotoxicity against human Caco2 cells after 3 to 4 days	[PMID: 20047920]
CCRF-CEM	CC₅₀	>100 μM Compound: Pradimicin A	Cytotoxicity against human CEM cells assessed as cell count after 3 days Cytotoxicity against human CEM cells assessed as cell count after 3 days	[PMID: 26513643]
CCRF-CEM	CC₅₀	>100 μM Compound: PRM-A	Cytotoxicity against human CEM cells after 7 days by trypan blue staining Cytotoxicity against human CEM cells after 7 days by trypan blue staining	[PMID: 20047920]
CCRF-CEM	CC₅₀	>100 μM Compound: Pradimicin	Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation	[PMID: 25617695]
CCRF-CEM	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human CD4+ T-lymphocyte CEM cells Cytotoxicity against human CD4+ T-lymphocyte CEM cells	[PMID: 26540494]
CCRF-CEM	EC₅₀	>50 μM Compound: PRM-A	Antiviral activity against HIV-1 3B harboring wild type gp120 infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis Antiviral activity against HIV-1 3B harboring wild type gp120 infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis	[PMID: 20047920]
CCRF-CEM	EC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human CEM cells after 4 days by by Coulter counter analysis Cytotoxicity against human CEM cells after 4 days by by Coulter counter analysis	[PMID: 21749165]
CCRF-CEM	EC₅₀	3.3 μM Compound: Pradimicin	Antiviral activity against HIV1 3B infected in human CEM cells assessed as reduction in virus-induced cytopathicity after 4 to 5 days by microscopy based syncytium cell formation assay Antiviral activity against HIV1 3B infected in human CEM cells assessed as reduction in virus-induced cytopathicity after 4 to 5 days by microscopy based syncytium cell formation assay	[PMID: 25617695]
CCRF-CEM	EC₅₀	3.3 μM Compound: Pradimicin A	Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis	[PMID: 26513643]
CCRF-CEM	EC₅₀	3.4 μM Compound: PRM-A	Antiviral activity against HIV1 3B infected in human CD4+ T-lymphocyte CEM cells assessed as inhibition of virus-induced cytopathicity after 4 to 5 days by microscopic analysis Antiviral activity against HIV1 3B infected in human CD4+ T-lymphocyte CEM cells assessed as inhibition of virus-induced cytopathicity after 4 to 5 days by microscopic analysis	[PMID: 26540494]
CCRF-CEM	EC₅₀	4.3 μM Compound: PRM-A	Antiviral activity against SIV mac251 infected in human HUT78 cells assessed as prevention of syncytium formation between persistently SIV mac251-infected HUT-78 cells and uninfected CEM cells after 3 to 4 days by ELISA Antiviral activity against SIV mac251 infected in human HUT78 cells assessed as prevention of syncytium formation between persistently SIV mac251-infected HUT-78 cells and uninfected CEM cells after 3 to 4 days by ELISA	[PMID: 20047920]
CCRF-CEM	EC₅₀	5.2 μM Compound: PRM-A	Antiviral activity against compound pretreated HIV-1 3B isolate 42 harboring gp120 mutant infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis Antiviral activity against compound pretreated HIV-1 3B isolate 42 harboring gp120 mutant infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis	[PMID: 20047920]
CCRF-CEM	EC₅₀	5.2 μM Compound: PRM-A	Antiviral activity against HIV-2 ROD infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis Antiviral activity against HIV-2 ROD infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis	[PMID: 20047920]
CCRF-CEM	EC₅₀	5.2 μM Compound: PRM-A	Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 4 days Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 4 days	[PMID: 21749165]
CCRF-CEM	EC₅₀	5.9 μM Compound: Pradimicin	Antiviral activity against HIV2 ROD infected in human CEM cells assessed as reduction in virus-induced cytopathicity after 4 to 5 days by microscopy based syncytium cell formation assay Antiviral activity against HIV2 ROD infected in human CEM cells assessed as reduction in virus-induced cytopathicity after 4 to 5 days by microscopy based syncytium cell formation assay	[PMID: 25617695]
CCRF-CEM	EC₅₀	5.9 μM Compound: Pradimicin A	Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis	[PMID: 26513643]
CCRF-CEM	EC₅₀	5.9 μM Compound: PRM-A	Antiviral activity against HIV-1 3B infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis Antiviral activity against HIV-1 3B infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis	[PMID: 20047920]
CCRF-CEM	EC₅₀	5.9 μM Compound: PRM-A	Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 4 days Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced cytopathicity after 4 days	[PMID: 21749165]
HeLa	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human HeLa cells after 3 to 4 days Cytotoxicity against human HeLa cells after 3 to 4 days	[PMID: 20047920]
L1210	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against mouse L1210 cells after 3 to 4 days Cytotoxicity against mouse L1210 cells after 3 to 4 days	[PMID: 20047920]
MOLT-4	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human Molt4 cells after 3 to 4 days Cytotoxicity against human Molt4 cells after 3 to 4 days	[PMID: 20047920]
MT4	CC₅₀	>100 μM Compound: PRM-A	Cytotoxicity against human MT4 cells assessed as reduction in cell viability measured after 5 days by MTS/PES assay Cytotoxicity against human MT4 cells assessed as reduction in cell viability measured after 5 days by MTS/PES assay	[PMID: 31809045]
MT4	CC₅₀	>100 μM Compound: PRM-A	Cytotoxicity against human MT4 cells assessed as reduction in cell viability measured after 5 days by MTS/PES assay Cytotoxicity against human MT4 cells assessed as reduction in cell viability measured after 5 days by MTS/PES assay	[PMID: 34229438]
MT4	CC₅₀	>100 μM Compound: PRM-A	Cytotoxicity against human MT4 cells assessed as cell viability measured after 5 days by MTS assay Cytotoxicity against human MT4 cells assessed as cell viability measured after 5 days by MTS assay	[PMID: 35512567]
MT4	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human MT4 cells after 7 days by trypan blue staining Cytotoxicity against human MT4 cells after 7 days by trypan blue staining	[PMID: 20047920]
MT4	EC₅₀	5 μM Compound: PRM-A	Antiviral activity against HIV-2 ROD infected in human MT4 cells assessed as inhibition of virus-induced cytopathicity after 7 days by trypan blue staining Antiviral activity against HIV-2 ROD infected in human MT4 cells assessed as inhibition of virus-induced cytopathicity after 7 days by trypan blue staining	[PMID: 20047920]
MT4	EC₅₀	5.2 μM Compound: PRM-A	Antiviral activity against HIV-1 3B infected in human MT4 cells assessed as inhibition of virus-induced cytopathicity after 7 days by trypan blue staining Antiviral activity against HIV-1 3B infected in human MT4 cells assessed as inhibition of virus-induced cytopathicity after 7 days by trypan blue staining	[PMID: 20047920]
MT4	EC₅₀	5.5 μM Compound: PRM-A	Antiviral activity against SIV mac251 infected in human MT4 cells assessed as inhibition of virus-induced cytopathicity after 7 days by trypan blue staining Antiviral activity against SIV mac251 infected in human MT4 cells assessed as inhibition of virus-induced cytopathicity after 7 days by trypan blue staining	[PMID: 20047920]
OST	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human thymidine kinase-negative OST cells after 3 to 4 days Cytotoxicity against human thymidine kinase-negative OST cells after 3 to 4 days	[PMID: 20047920]
PBMC	CC₅₀	>250 μM Compound: PRM-A	Cytotoxicity against human PBMC after 7 days by trypan blue staining Cytotoxicity against human PBMC after 7 days by trypan blue staining	[PMID: 20047920]
PBMC	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human PBMC cells after 3 to 4 days Cytotoxicity against human PBMC cells after 3 to 4 days	[PMID: 20047920]
PBMC	EC₅₀	>50 μM Compound: PRM-A	Antiviral activity against HIV-1 3B cells infected in human PBMC cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis Antiviral activity against HIV-1 3B cells infected in human PBMC cells assessed as inhibition of virus-induced cytopathicity after 3 to 4 days by microscopic analysis	[PMID: 20047920]
Raji	EC₅₀	3.4 μM Compound: PRM-A	Antiviral activity against compound pretreated X4 tropic HIV-1 3B infected in human Raji cells expressing DC-SIGN gene assessed as prevention of syncytium formation between persistently HIV-1 3B-infected Raji cells and uninfected human C8166 cells after 4 Antiviral activity against compound pretreated X4 tropic HIV-1 3B infected in human Raji cells expressing DC-SIGN gene assessed as prevention of syncytium formation between persistently HIV-1 3B-infected Raji cells and uninfected human C8166 cells after 4	[PMID: 20047920]
Raji	EC₅₀	5.4 μM Compound: PRM-A	Antiviral activity against X4 tropic HIV-1 3B infected in human Raji cells expressing DC-SIGN gene assessed as prevention of syncytium formation between persistently HIV-1 3B-infected Raji cells and uninfected human C8166 cells after 36 to 42 hrs by micro Antiviral activity against X4 tropic HIV-1 3B infected in human Raji cells expressing DC-SIGN gene assessed as prevention of syncytium formation between persistently HIV-1 3B-infected Raji cells and uninfected human C8166 cells after 36 to 42 hrs by micro	[PMID: 20047920]
Raji	IC₅₀	16 μM Compound: PRM-A	Antiviral activity against SIV mac251 infected in human Raji cells expressing DC-SIGN gene assessed as inhibition of virus capture by Raji cells after 60 mins by ELISA Antiviral activity against SIV mac251 infected in human Raji cells expressing DC-SIGN gene assessed as inhibition of virus capture by Raji cells after 60 mins by ELISA	[PMID: 20047920]
Raji	IC₅₀	16 μM Compound: PRM-A	Antiviral activity against SIV mac251 infected in human Raji cells expressing DC-SIGN gene assessed as prevention of syncytium formation between persistently HIV-1 3B-infected Raji cells and uninfected human C8166 cells after 60 mins by ELISA Antiviral activity against SIV mac251 infected in human Raji cells expressing DC-SIGN gene assessed as prevention of syncytium formation between persistently HIV-1 3B-infected Raji cells and uninfected human C8166 cells after 60 mins by ELISA	[PMID: 20047920]
Raji	IC₅₀	21 μM Compound: PRM-A	Antiviral activity against R5 tropic HIV-1 Bal infected in human Raji cells expressing DC-SIGN gene assessed as inhibition of virus capture by Raji cells after 60 mins by ELISA Antiviral activity against R5 tropic HIV-1 Bal infected in human Raji cells expressing DC-SIGN gene assessed as inhibition of virus capture by Raji cells after 60 mins by ELISA	[PMID: 20047920]
Raji	IC₅₀	3.5 μM Compound: PRM-A	Antiviral activity against X4 tropic HIV-1 3B infected in human Raji cells expressing DC-SIGN gene assessed as inhibition of virus capture by Raji cells after 60 mins by ELISA Antiviral activity against X4 tropic HIV-1 3B infected in human Raji cells expressing DC-SIGN gene assessed as inhibition of virus capture by Raji cells after 60 mins by ELISA	[PMID: 20047920]
SUP-T1	EC₅₀	3.4 μM Compound: PRM-A	Antiviral activity against HIV-1 3B infected in human HUT78 cells assessed as prevention of syncytium formation between persistently HIV-1 3B-infected HUT-78 cells and uninfected SupT1 cells after 3 to 4 days by ELISA Antiviral activity against HIV-1 3B infected in human HUT78 cells assessed as prevention of syncytium formation between persistently HIV-1 3B-infected HUT-78 cells and uninfected SupT1 cells after 3 to 4 days by ELISA	[PMID: 20047920]
U-87MG ATCC	CC₅₀	>50 μM Compound: PRM-A	Cytotoxicity against human U87 cells after 3 to 4 days Cytotoxicity against human U87 cells after 3 to 4 days	[PMID: 20047920]

In Vitro

Pradimicin A (48 h) inhibits the growth of Candida rugosa with a minimum inhibitory concentration (MIC) of 4 μg/mL, and completely inhibits Candida rugosa growth while showing preferential binding to branched oligomannose motifs 6 and 7 (MAC = 1 mM) relative to other tested glycan structures^[1]^[3].
Pradimicin A (0.3-100 μM; 1 h pre-incubation, 3 days post challenge) inhibits SARS-CoV-2 infection of Calu-3 cells with an IC₅₀ of 1.2 μM, shows no cytotoxicity at concentrations up to 100 μM, and its antiviral activity is dependent on binding to branched oligomannose motifs on viral spike proteins^[1].
Pradimicin A (1 mM) shows Ca²⁺‑dependent specific binding to Man-OMe (100 mM) with two distinct binding sites in ITC assays (40 injections, 30 °C). The primary binding (K_a = 10400 M⁻¹) is approximately 40‑fold stronger than the secondary binding (K_a = 263 M⁻¹)^[2].
Pradimicin A (1 mM) binds methyl α-D-mannopyranoside in a cell-free buffer system with a primary dissociation constant (K_d1) of 96 μM and a secondary dissociation constant (K_d2) of 3800 μM^[3].
Pradimicin A (0.8-12.5 μg/mL) exhibits broad-spectrum antifungal activity against diverse fungal species including Candida albicans A9540^[5].
Pradimicin A exhibits antiviral activity against coronaviruses and HIV-1, targeting viral glycoprotein mannose moieties and demonstrating a high genetic barrier to HIV-1 resistance^[5].

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

Chemical Information

CAS No. 117704-65-1
분자량 840.78
화학식 C₄₀H₄₄N₂O₁₈
SMILES

OC1=C2C3=C(O)C(C(N[C@H](C)C(O)=O)=O)=C(C)C=C3[C@@H]([C@H](C2=CC4=C1C(C5=CC(OC)=CC(O)=C5C4=O)=O)O)O[C@H]6[C@@H]([C@H]([C@H]([C@H](O6)C)NC)O[C@H]7[C@@H]([C@H]([C@@H](CO7)O)O)O)O
선적

Room temperature in continental US; may vary elsewhere.
보관

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

순도&문서

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (277 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Nakagawa Y, et al. Molecular basis of N-glycan recognition by pradimicin a and its potential as a SARS-CoV-2 entry inhibitor. Bioorg Med Chem. 2024 May 1;105:117732. [Content Brief]

[2]. Nakagawa Y, et al. Mapping of the primary mannose binding site of pradimicin A. J Am Chem Soc. 2011;133(43):17485-17493. [Content Brief]

[3]. Miyanishi W, et al. d-Mannose binding, aggregation property, and antifungal activity of amide derivatives of pradimicin A. Bioorg Med Chem. 2022;55:116590. [Content Brief]

[4]. Nakagawa Y, et al. Molecular Basis of Mannose Recognition by Pradimicins and their Application to Microbial Cell Surface Imaging. Cell Chem Biol. 2019;26(7):950-959.e8. [Content Brief]

[5]. Guo Y, et al. Isolation, biosynthesis, and biological activity of pradimicins from actinomycetes. Bioorg Chem. 2025;164:108884. [Content Brief]

Calculators

몰농도 계산기

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

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

농도 희석 계산기

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

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

상품명:
Cat. No.:
수량:
MCE Japan Authorized Agent:

상품명:
CAS No.:
Species:
Purity:
수량:

Pradimicin A

All HIV Isoforms