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36051-31-7

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36051-31-7 Usage

Uses

Guanosine 5′-triphosphate sodium salt solution has been used for reconstituting transducin during purification of transducin.

General Description

GTP is supplied as the disodium salt in crystal form.

Biochem/physiol Actions

GTP functions as a carrier of phosphates and pyrophosphates involved in channeling chemical energy into specific biosynthetic pathways. GTP activates the signal transducing G proteins which are involved in various cellular processes including proliferation, differentiation, and activation of several intracellular kinase cascades. Proliferation and apoptosis are regulated in part by the hydrolysis of GTP by small GTPases Ras and Rho. Another type of small GTPase, Rab, plays a role in the docking and fusion of vesicles and may also be involved in vesicle formation. In addition to its role in signal transduction, GTP also serves as an energy-rich precursor of mononucleotide units in the enzymatic biosynthesis of DNA and RNA.

Check Digit Verification of cas no

The CAS Registry Mumber 36051-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,5 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36051-31:
(7*3)+(6*6)+(5*0)+(4*5)+(3*1)+(2*3)+(1*1)=87
87 % 10 = 7
So 36051-31-7 is a valid CAS Registry Number.

36051-31-7 Well-known Company Product Price

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  • (Code)Product description
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  • Roche

  • (10106399001)  GTP  Disodium salt

  • 36051-31-7

  • 000000010106399001

  • 1,703.52CNY

  • Detail
  • Sigma

  • (G8877)  Guanosine5′-triphosphatesodiumsalthydrate  ≥95% (HPLC), powder

  • 36051-31-7

  • G8877-10MG

  • 349.83CNY

  • Detail
  • Sigma

  • (G8877)  Guanosine5′-triphosphatesodiumsalthydrate  ≥95% (HPLC), powder

  • 36051-31-7

  • G8877-25MG

  • 604.89CNY

  • Detail
  • Sigma

  • (G8877)  Guanosine5′-triphosphatesodiumsalthydrate  ≥95% (HPLC), powder

  • 36051-31-7

  • G8877-100MG

  • 1,419.21CNY

  • Detail
  • Sigma

  • (G8877)  Guanosine5′-triphosphatesodiumsalthydrate  ≥95% (HPLC), powder

  • 36051-31-7

  • G8877-250MG

  • 2,377.44CNY

  • Detail
  • Sigma

  • (G8877)  Guanosine5′-triphosphatesodiumsalthydrate  ≥95% (HPLC), powder

  • 36051-31-7

  • G8877-1G

  • 6,762.60CNY

  • Detail

36051-31-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Guanosine 5′-triphosphate sodium salt hydrate

1.2 Other means of identification

Product number -
Other names trisodium,[[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] hydrogen phosphate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36051-31-7 SDS

36051-31-7Downstream Products

36051-31-7Relevant articles and documents

Convenient syntheses of cytidine 5'-triphosphate, guanosine 5'-triphosphate, and uridine 5'-triphosphate and their use in the preparation of UDP-glucose, UDP-glucuronic acid, and GDP-mannose

Simon,Grabowski,Whitesides

, p. 1834 - 1841 (2007/10/02)

This paper compares enzymatic and chemical methods for the synthesis of cytidine 5'-triphosphate, guanosine 5'-triphosphate, and uridine 5'-triphosphate from the corresponding nucleoside monophosphates on scales of ~10 g. These nucleoside triphosphates are important as intermediates in Leloir pathway biosyntheses of complex carbohydrates; the nucleoside monophosphates are readily available commercially. The best route to CTP is based on phosphorylation of CMP using adenylate kinase (EC 2.7.4.3); the route to GTP involves phosphorylation of GMP using guanylate kinase (EC 2.7.4.8); chemical deamination of CTP (prepared enzymatically from CMP) is the best synthesis of UTP. For the 10-200-mmol-scale reactions described in this paper, it is more convenient to prepare phosphoenolpyruvate (PEP), used in the enzymatic preparations, from D-(-)-3-phosphoglyceric acid (3-PGA) in the reaction mixture rather than to synthesize PEP in a separate chemical step. The in situ conversion of 3-PGA to PEP requires the coupled action of phosphoglycerate mutase (EC 2.7.5.3) and enolase (EC 4.2.1.11). The enzyme-catalyzed syntheses of uridine 5'-diphosphoglucose (UDP-Glc), uridine 5'-diphosphoglucuronic acid (UDP-GlcUA), and guanosine 5'-diphosphomannose (GDP-Man) illustrate the use of the nucleoside triphosphates.

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