5-PROPYNYLURACIL

CC#CC1=CNC(=O)NC1=O

InChIKey=UJBCLAXPPIDQEE-UHFFFAOYSA-N

InChI=1S/C7H6N2O2/c1-2-3-5-4-8-7(11)9-6(5)10/h4H,1H3,(H2,8,9,10,11)

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Efficient and rapid template-directed nucleic acid copying using 2'-amino-2',3'-dideoxyribonucleoside-5'-phosphorimidazolide monomers.	2009-10-14	19757789
Enzymatic primer-extension with glycerol-nucleoside triphosphates on DNA templates.	2009	19305495
PNA-DNA chimeras containing 5-alkynyl-pyrimidine PNA units. Synthesis, binding properties, and enzymatic stability.	2003-10	14609235
5-propynyluracil.diaminopurine: an efficient base-pair for non-enzymatic transcription of DNA.	2002-08-07	12170785
Multiple dose netivudine, a potent anti-varicella zoster virus agent, in healthy elderly volunteers and patients with shingles.	1996-03	9182115

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:29:52 GMT 2025` Edited by `admin` on `Mon Mar 31 21:29:52 GMT 2025`
Record UNII	90NI1ZDQ6N
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

5-PROPYNYLURACIL

Systematic Name

English

2,4(1H,3H)-PYRIMIDINEDIONE, 5-(1-PROPYNYL)-

Preferred Name

English

5-(1-PROPYNYL)URACIL

Systematic Name

English

Code System Code Type Description

FDA UNII

90NI1ZDQ6N

Created by admin on Mon Mar 31 21:29:52 GMT 2025 , Edited by admin on Mon Mar 31 21:29:52 GMT 2025

PRIMARY

PUBCHEM

131813

Created by admin on Mon Mar 31 21:29:52 GMT 2025 , Edited by admin on Mon Mar 31 21:29:52 GMT 2025

PRIMARY

CAS

134700-29-1

Created by admin on Mon Mar 31 21:29:52 GMT 2025 , Edited by admin on Mon Mar 31 21:29:52 GMT 2025

PRIMARY

EPA CompTox

DTXSID10158869

Created by admin on Mon Mar 31 21:29:52 GMT 2025 , Edited by admin on Mon Mar 31 21:29:52 GMT 2025

PRIMARY