Golotimod TFA

SKU:BHB21901300
Overview
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Golotimod TFA (CAS 2828433-07-2) is an inhibitor. Reported to act on STAT3. Relevant to Anti-infection and Stem Cell/Wnt research. Molecular formula C18H20F3N3O7, molecular weight 447.36 g/mol.
CAS Number 2828433-07-2
Molecular Weight 447.36 g/mol
Target STAT3
Storage See Certificate of Analysis
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Catalog no. Size
HY-14743A-50MG 50 mg
HY-14743A-100MG 100 mg
HY-14743A-250MG 250 mg
Available Options

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  • Options: Size: 50 mg, 100 mg, 250 mg
  • Lead time: confirmed on inquiry for every option.
  • Storage: Please store the product under the recommended conditions in the Certificate of Analysis.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: store as stated on the Certificate of Analysis; contact us if you need the condition before ordering.
Field Specification
Target STAT3
Alternative names SCV 07 TFA; Gamma-D-glutamyl-L-tryptophan TFA
CAS no. 2828433-07-2
Applications
  • Functional Assay (In Vitro)
Molecular weight 447.36
Molecular formula C18H20F3N3O7
SMILES O=C(CC[C@@](N)(C(O)=O)[H])N[C@]([H])(C(O)=O)CC1=CNC2=C1C=CC=C2.OC(C(F)(F)F)=O
Storage Refer to Certificate of Analysis (CoA) for storage conditions
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-14743A
Main SKU BHB21901300
Inhibitors

Compound Overview

Golotimod TFA, also known as SCV 07 TFA or Gamma-D-glutamyl-L-tryptophan TFA, is an immunomodulating peptide with antimicrobial activity that increases the efficacy of antituberculosis therapy, stimulates thymic and splenic cell proliferation, and improves macrophage function. It inhibits STAT3 signaling and modulates the duration and severity of oral mucositis in animal models given radiation or radiation combined with Cisplatin, and it is also a potential therapeutic for recurrent genital herpes simplex virus type 2 (HSV-2)[1][2][3]. It has the molecular formula C18H20F3N3O7 (MW 447.36).

Physical & Chemical Properties

CAS Number 2828433-07-2
Molecular Formula C18H20F3N3O7
Molecular Weight 447.36 g/mol
SMILES O=C(CC[C@@](N)(C(O)=O)[H])N[C@]([H])(C(O)=O)CC1=CNC2=C1C=CC=C2.OC(C(F)(F)F)=O
Target STAT3
Signaling Pathway Anti-infection; Stem Cell/Wnt; JAK/STAT Signaling
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Rose WA 2nd, et al. An immunomodulating dipeptide, SCV-07, is a potential therapeutic for recurrent genital herpes simplex virus type 2 (HSV-2). Int J Antimicrob Agents. 2008 Sep;32(3):262-6.

[2]. Geiger JL, et al. The STAT3 pathway as a therapeutic target in head and neck cancer: Barriers and innovations. Oral Oncol. 2016 May;56:84-92.

[3]. Watkins B, et al. Attenuation of radiation- and chemoradiation-induced mucositis using gamma-D-glutamyl-L-tryptophan (SCV-07). Oral Dis. 2010 Oct;16(7):655-60.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with your institution's chemical hygiene plan.

In Vivo

In female Hartley guinea pigs, Golotimod (SCV-07) TFA (100 μg/kg, 5 days; oral gavage or subcutaneous injection) reduces experimental recurrent genital HSV-2 disease with oral administration; more importantly, oral SCV07 after fasting gives a greater reduction in incidence and severity than SCV-07 without fasting[1]. In male LVG golden Syrian hamsters, Golotimod (SCV-07) TFA (100 μg/kg, subcutaneous injection once or twice a day from days 1 to 20) can lessen the severity and duration of oral mucositis (OM) induced by acute and split radiation, and shorten the duration of ulcerative OM[3].

Animal ModelFemale Hartley guinea pigs (250-300 g) infected HSV-2[1]
Dosage100 μg/kg
AdministrationOral gavage or subcutaneous injection; 5 days
ResultReduced incidence of lesions from 55% (one week before treatment) to only 18% by oral administration, and showed no significant reduction in disease by subcutaneous injection of SCV-07.
Animal ModelMale LVG golden Syrian Hamsters weighing approximately 80 g with radiation-induced mucositis[3]
Dosage10, 100 μg/kg or 1 mg/kg
AdministrationSubcutaneous injection; once or twice a day from days 1 to 20
ResultShowed a peak mucositis of 3.0 on day 18 in the control group compared to only 2.2 in the test group, and the mucositis score in the SCV-07 treated hamsters was only 6.3% compared to 28.1% in the control group at dose of 100 μg/kg. Significantly decreased the severity and duration of oral mucositis (OM) at dose of 10 μg/kg, 100 μg/kg or 1 mg/kg.

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price listed?
A.Every size of this product is quoted on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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