Prumycin

    WARNING: This product is for research use only, not for human or veterinary use.

Hodoodo CAT#: H596862

CAS#: 38819-28-2

Description: Prumycin is an antifungal antibiotic.

Chemical Structure

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Prumycin
CAS# 38819-28-2
Instruction

Theoretical Analysis

Hodoodo Cat#: H596862
Name: Prumycin
CAS#: 38819-28-2
Chemical Formula: C8H17N3O4
Exact Mass: 219.12
Molecular Weight: 219.240
Elemental Analysis: C, 43.83; H, 7.82; N, 19.17; O, 29.19

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @hodoodo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: Prumycin; EINECS 254-134-1;

IUPAC/Chemical Name: (R)-2-amino-N-((2S,3R,4R)-4-amino-1,3-dihydroxy-5-oxopentan-2-yl)propanamide

InChi Key: KBSVAZCLQHOLKP-JRTVQGFMSA-N

InChi Code: InChI=1S/C8H17N3O4/c1-4(9)8(15)11-6(3-13)7(14)5(10)2-12/h2,4-7,13-14H,3,9-10H2,1H3,(H,11,15)/t4-,5+,6+,7-/m1/s1

SMILES Code: O=C[C@H](N)[C@H]([C@@H](NC([C@H](N)C)=O)CO)O

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 219.24 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

Molarity Calculator

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Reconstitution Calculator

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1: Tanaka K, Fukuda M, Amaki Y, Sakaguchi T, Inai K, Ishihara A, Nakajima H. Importance of prumycin produced by Bacillus amyloliquefaciens SD-32 in biocontrol against cucumber powdery mildew disease. Pest Manag Sci. 2017 Dec;73(12):2419-2428. doi: 10.1002/ps.4630. Epub 2017 Aug 29. PubMed PMID: 28560847.

2: Kumari M, Chandra S, Tiwari N, Subbarao N. High Throughput Virtual Screening to Identify Novel natural product Inhibitors for MethionyltRNA-Synthetase of Brucella melitensis. Bioinformation. 2017 Jan 20;13(1):8-16. doi: 10.6026/97320630013008. eCollection 2017. PubMed PMID: 28479744; PubMed Central PMCID: PMC5405087.

3: Otoguro K, Ishiyama A, Kobayashi M, Sekiguchi H, Izuhara T, Sunazuka T, Tomoda H, Yamada H, Omura S. In vitro and in vivo antimalarial activities of a carbohydrate antibiotic, prumycin, against drug-resistant strains of Plasmodia. J Antibiot (Tokyo). 2004 Jun;57(6):400-2. PubMed PMID: 15323130.

4: Hamada M, Ikeda T, Manabe M, Gomi S, Kondo S, Takeuchi T, Umezawa H. Prumycin produced by Bacillus cereus. J Antibiot (Tokyo). 1983 Jan;36(1):86. PubMed PMID: 6432762.

5: Okubo S, Morimoto M, Mineura K, Marumo H, Omura S. Studies on antitumor activity of prumycin. IV. Effect of prumycin on mouse immune system. J Antibiot (Tokyo). 1980 Feb;33(2):231-5. PubMed PMID: 7380733.

6: Okubo S, Nakamura N, Morimoto M, Mineura K, Marumo H, Omura S. Studies on antitumor activity of prumycin. II. Studies on distribution and excretion of prumycin. J Antibiot (Tokyo). 1980 Feb;33(2):221-5. PubMed PMID: 7380732.

7: Okubo S, Nakamura N, Morimoto M, Mineura K, Marumo H, Omura S. Studies on antitumor activity of prumycin. III. Mode of action of prumycin on HeLa S-3 cells. J Antibiot (Tokyo). 1980 Feb;33(2):226-30. PubMed PMID: 6155368.

8: Okubo S, Nakamura N, Ito K, Marumo H, Tanaka M, Omura S. Antitumor activity of prumycin. J Antibiot (Tokyo). 1979 Apr;32(4):347-54. PubMed PMID: 468722.

9: Hasegawa A, Aritake N, Kiso M. Synthesis of prumycin and related compounds. Carbohydr Res. 1976 Dec;52:137-49. PubMed PMID: 1016984.

10: Hasegawa A, Aritake N, Kiso M. A new synthesis of prumycin. Carbohydr Res. 1976 Oct;51(1):C10-C12. PubMed PMID: 1000523.

11: Schwartz JL, Katagiri M, Omura S, Tishler M. The mechanism of prumycin action. J Antibiot (Tokyo). 1974 Jun;27(6):379-85. PubMed PMID: 4854949.

12: Omura S, Katagiri M, Atsumi K, Hata T, Jakubowski AA, Springs EB, Tishler M. Structure of prumycin. J Chem Soc Perkin 1. 1974;0(14):1627-31. PubMed PMID: 4472323.

13: Hata T, Omura S, Katagiri M, Atsumi K, Awaya J. A new antifungal antibiotic, prumycin. J Antibiot (Tokyo). 1971 Dec;24(12):900-1. PubMed PMID: 5140535.