7-Methyl-5′-guanylic acid

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C11H17N5O8P
Molecular Weight	378.2551
Optical Activity	UNSPECIFIED
Defined Stereocenters	4 / 4
E/Z Centers	0
Charge	1

SHOW SMILES / InChI

Structure Search

SMILES

C[N+]1=CN([C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)C3=C1C(=O)N=C(N)N3

InChI

InChIKey=AOKQNZVJJXPUQA-KQYNXXCUSA-O

InChI=1S/C11H16N5O8P/c1-15-3-16(8-5(15)9(19)14-11(12)13-8)10-7(18)6(17)4(24-10)2-23-25(20,21)22/h3-4,6-7,10,17-18H,2H2,1H3,(H4-,12,13,14,19,20,21,22)/p+1/t4-,6-,7-,10-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C11H17N5O8P
Molecular Weight	378.2551
Charge	1
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	4 / 4
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 15:33:57 GMT 2023` Edited by `admin` on `Sat Dec 16 15:33:57 GMT 2023`
Record UNII	M5SL28EU5R
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

7-Methyl-5′-guanylic acid

Common Name

English

7-Methyl-5′-GMP

Common Name

English

1H-Purinium, 2-amino-6,9-dihydro-7-methyl-6-oxo-9-(5-O-phosphono-β-D-ribofuranosyl)-

Systematic Name

English

m7GMP

Common Name

English

2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl]-7-methyl-6-oxo-6,9-dihydro-1H-purin-7-ium

Systematic Name

English

9H-Purinium, 2-amino-1,6-dihydro-7-methyl-6-oxo-9-β-D-ribofuranosyl-, 5′-(dihydrogen phosphate)

Systematic Name

English

5′-Guanylic acid, 7-methyl-

Common Name

English

((2R,3S,4R,5R)-5-(2-amino-7-methyl-6-oxo-1,6,7,8-tetrahydro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate

Systematic Name

English

Code System Code Type Description

PUBCHEM

135398701

Created by admin on Sat Dec 16 15:33:57 GMT 2023 , Edited by admin on Sat Dec 16 15:33:57 GMT 2023

PRIMARY

EPA CompTox

DTXSID80906399

Created by admin on Sat Dec 16 15:33:57 GMT 2023 , Edited by admin on Sat Dec 16 15:33:57 GMT 2023

PRIMARY

FDA UNII

M5SL28EU5R

Created by admin on Sat Dec 16 15:33:57 GMT 2023 , Edited by admin on Sat Dec 16 15:33:57 GMT 2023

PRIMARY

CAS

47442-17-1

Created by admin on Sat Dec 16 15:33:57 GMT 2023 , Edited by admin on Sat Dec 16 15:33:57 GMT 2023

PRIMARY

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