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TUBERCIDIN

TUBERCIDIN Suppliers list
Company Name: Wuhu Nuowei Chemical Technology Co., Ltd  Gold
Tel: 0553-8233716 18055326116
Email: sales@nuowei-chem.com
Company Name: Maanshan geneyan biotech Co.,LTD  Gold
Tel: 18913822354
Email: market@geneyan-bio.com
Company Name: Nanjing Baifuli Technology Co., Ltd.  Gold
Tel: 25-25-58740604 15951658055
Email: sales@unisyn.cn
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Innochem(Beijing) Technology Co.,Ltd.  
Tel: 010-56541685 13070143590
Email: sales@innochem.cn

TUBERCIDIN manufacturers

  • 7-Deaza-adeonsine
  • 7-Deaza-adeonsine pictures
  • 2026-09-17
  • CAS:69-33-0
  • Min. Order: 10g
  • Purity: 97%min
  • Supply Ability: 100kgs
  • Tubercidin
  • Tubercidin pictures
  • $48.00
  • 2026-08-20
  • CAS:69-33-0
  • Purity: 99.83%
  • Supply Ability: 10g
  • TUBERCIDIN
  • TUBERCIDIN pictures
  • 2026-08-13
  • CAS:69-33-0
  • Min. Order: 1G
  • Purity: 98%
  • Supply Ability: 2000
TUBERCIDIN Basic information
Product Name:TUBERCIDIN
Synonyms:TUBERCIDIN;TUBERCIDINE;3-d)pyrimidin-4-amine,7-beta-d-ribofuranosyl-7h-pyrrolo(;3-d)pyrimidine,4-amino-7-beta-d-ribofuranosyl-7h-pyrrolo(;4-amino-7-(beta-d-ribofuranosyl)-pyrrolo(2,3-d)pyrimidine;4-amino-7-beta-d-ribofuranosyl-7h-pyrrolo(2,3-d)pyrimidine;7-beta-d-ribofuranosyl-7h-pyrrolo(2,3-d)pyrimidine-4-amine;7-deaza-adenosin
CAS:69-33-0
MF:C11H14N4O4
MW:266.25
EINECS:200-703-4
Product Categories:
Mol File:69-33-0.mol
TUBERCIDIN Structure
TUBERCIDIN Chemical Properties
Melting point 247-248 °C (decomp)(Solv: water (7732-18-5))
alpha D17 -67° (50% acetic acid)
Boiling point 409.46°C (rough estimate)
density 1.2896 (rough estimate)
refractive index 1.8340 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Soluble in DMSO
form powder
pka12.44±0.70(Predicted)
color off-white
Merck 13,9875
BRN 38498
Stability:Hygroscopic
InChIKeyHDZZVAMISRMYHH-UIRWVKCDSA-N
CAS DataBase Reference69-33-0
Safety Information
Hazard Codes T+
Risk Statements 28
Safety Statements 36/37/39-45
RIDADR UN 3462 6.1/PG 2
WGK Germany 3
RTECS UY8870000
10
HazardClass 6.1(a)
PackingGroup II
HS Code 29419090
ToxicityLD50 i.v. in mice: 45 mg/kg (Anzai)
MSDS Information
ProviderLanguage
SigmaAldrich English
TUBERCIDIN Usage And Synthesis
Chemical PropertiesWhite crystal
UsesTubercidin is a nucleoside metabolite first isolated from Streptomyces tubericidus. Tubercidin, like other nucleosides, is a broad spectrum, potent chemotherapeutic agent active against viruses, bacteria, fungi, protozoans and tumours. Tubercidin acts at a diverse range of sites, such as RNA processing, nucleic acid and protein synthesis, and acts as a nucleoside mimic of adenosine.
DefinitionChEBI: An N-glycosylpyrrolopyrimidine that is adenosine in which the in the 5-membered ring that is not attached to the ribose moiety is replaced by a carbon. Tubercidin is produced in the culture broth of Streptomyces tubericidus.
Biological Activitytubercidin is an adenosine analog antibiotic agent.nucleoside antibiotics are a family of natural products with various biological functions. their biosynthesis is a complex process via multistep enzymatic reactions.
in vitroprevious study showed that tubercidin alone had a dose-dependent inhibitory effect on myeloid and erythroid human bone marrow progenitor cells. bfu-e were more sensitive at higher doses of tubercidin than cfu-gm. the 99% complete inhibition of bfu-e colonies was observed at 10 nm tubercidin, whereas complete inhibition of cfu-gm occurred at 100 nm [1].
in vivoanimal toxicity study showed that four successive daily injections of tubercidin at 5 mg/kg per day could produce 100% mouse mortality within 3 to 5 days, with massive peritonitis and intestinal obstruction. in addition, coadministration of nbmpr-p at 25 mg/kg per day could protect the mice from the tubercidin lethality and allow the repetition of the regimen for a second time with 100% survival [1].
IC 503.4 and 3.7 nm for granulocyte-macrophage cfu (cfu-gm) and erythroid burst-forming units (bfu-e), respectively
Purification Methods7-Deazaadenosine forms needles from hot H2O. It is soluble in H2O (0.33%), MeOH (0.5%) and EtOH (0.05%). It has UV max at 270nm ( 12,100) in 0.001N NaOH. The picrate has m 229-231o(dec). [Tolman et al. J Am Chem Soc 91 2102 1969, Mizuno et al. J Org Chem 28 3329 1963, IR: Anzai et al. J Antibiot (Japan) [9] 10 201 1957, Beilstein 26 IV 1117.]
references[1] el kouni mh,diop d,o'shea p,carlisle r,sommadossi jp. prevention of tubercidin host toxicity by nitrobenzylthioinosine 5'-monophosphate for the treatment of schistosomiasis. antimicrob agents chemother.1989 jun;33(6):824-7.
[2] grage tb,rochlin db,weiss aj,wilson wl. clinical studies with tubercidin administered after absorption into human erythrocytes. cancer res.1970 jan;30(1):79-81.
TUBERCIDIN Preparation Products And Raw materials
Preparation Products5-IODOTUBERCIDIN
Tag:TUBERCIDIN(69-33-0) Related Product Information
SANGIVAMYCIN API-2 Triciribine TUBERCIDIN tubercidin-5'-diphosphate 4-Amino-5-cyano-7-(beta-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine 7-Ch-cAMP sodium salt 7-Deaza-A CEP 5-IODOTUBERCIDIN tubercidin 5'-phosphate,TUBERCIDIN-5'-O-MONOPHOSPHATE SODIUM SALT,tubercidin-5-monophosphat thiosangivamycin ara-tubercidin tubercidin 5'-triphosphate ara-tubercidin 5'-triphosphate tubercidin 5'-diphosphate-5'-1,2-dipalmitin TUBERCIDIN, [5-3H] 7-Deaza-7-carbamoyladenosine hydrate Sangivamycin, [3H]-