A peptide ETB receptor agonist
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Sarafotoxin S6c (trifluoroacetate salt)

Item No. 30040

Product Insert (PDF)
Technical Information
Formal Name
L-cysteinyl-L-threonyl-L-cysteinyl-L-asparaginyl-L-α-aspartyl-L-methionyl-L-threonyl-L-α-aspartyl-L-α-glutamyl-L-α-glutamyl-L-cysteinyl-L-leucyl-L-asparaginyl-L-phenylalanyl-L-cysteinyl-L-histidyl-L-glutaminyl-L-α-aspartyl-L-valyl-L-isoleucyl-L-tryptophan, cyclic (1→15),(3→11)-bis(disulfide), trifluoroacetate salt
Synonyms
  • SRTX-c
  • STX-S6c
Molecular Formula
C103H147N27O37S5 • XCF3COOH
Formula Weight
Purity
≥98%
A solid
Peptide Sequence
CTCNDMTDEECLNFCHQDVIW-OH
DMSO: Sparingly Soluble: 1-10 mg/ml
SMILES
O=C(N[C@]([C@H](O)C)([H])C(N[C@@H](CSSC[C@H](N1)C(N[C@H](C(N[C@@H](CC(N)=O)C(N[C@H](C2=O)CC3=CC=CC=C3)=O)=O)CC(C)C)=O)C(N[C@@H](CC(N)=O)C(N[C@@H](CC(O)=O)C(N[C@@H](CCSC)C(N[C@]([C@H](O)C)([H])C(N[C@@H](CC(O)=O)C(N[C@@H](CCC(O)=O)C(N[C@@H](CCC(O)=O)C1=O)=O)=O)=O)=O)=O)=O)=O)=O)[C@H](CSSC[C@H](N2)C(N[C@@H](CC4=CNC=N4)C(N[C@@H](CCC(N)=O)C(N[C@@H](CC(O)=O)C(N[C@@H](C(C)C)C(N[C@@](C(N[C@@H](CC5=CNC6=C5C=CC=C6)C(O)=O)=O)([H])[C@@H](C)CC)=O)=O)=O)=O)=O)N[H].FC(F)(F)C(O)=O
InChi Code
InChI=1S/C103H147N27O37S5.C2HF3O2/c1-10-46(6)80(100(163)123-67(103(166)167)30-50-37-109-54-19-15-14-18-52(50)54)128-99(162)79(45(4)5)127-95(158)66(36-78(144)145)120-85(148)55(20-23-71(105)133)112-90(153)61(31-51-38-108-43-110-51)117-97(160)69-40-170-169-39-53(104)83(146)129-81(47(7)131)102(165)126-70-42-172-171-41-68(96(159)115-59(28-44(2)3)88(151)118-62(32-72(106)134)91(154)116-60(89(152)125-69)29-49-16-12-11-13-17-49)124-86(149)57(22-25-75(138)139)111-84(147)56(21-24-74(136)137)113-94(157)65(35-77(142)143)122-101(164)82(48(8)132)130-87(150)58(26-27-168-9)114-93(156)64(34-76(140)141)121-92(155)63(33-73(107)135)119-98(70)161;3-2(4,5)1(6)7/h11-19,37-38,43-48,53,55-70,79-82,109,131-132H,10,20-36,39-42,104H2,1-9H3,(H2,105,133)(H2,106,134)(H2,107,135)(H,108,110)(H,111,147)(H,112,153)(H,113,157)(H,114,156)(H,115,159)(H,116,154)(H,117,160)(H,118,151)(H,119,161)(H,120,148)(H,121,155)(H,122,164)(H,123,163)(H,124,149)(H,125,152)(H,126,165)(H,127,158)(H,128,162)(H,129,146)(H,130,150)(H,136,137)(H,138,139)(H,140,141)(H,142,143)(H,144,145)(H,166,167);(H,6,7)/t46-,47+,48+,53-,55-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,66-,67-,68-,69-,70-,79-,80-,81-,82-;/m0./s1
InChi Key
HWSGKTVIILWOKU-FRTCUJHUSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Cayman Chemical
    Visit Our Environmental Toxicology Resource Center

    Explore additional resources to study natural toxins, pollutants including PFAS and 6-PPD-Q, and their biological effects.

    ENVIRONMENTAL TOXICOLOGY TOOLS & SERVICES
    Product Description

    Sarafotoxin S6c is a snake venom-derived toxin and peptide endothelin type B (ETB) receptor agonist.1,2 It induces phosphatidyl inositol turnover in rat hippocampal slices, which endogenously express the ETB receptor, with an EC50 value of approximately 10 nM.2 Sarafotoxin S6c selectively binds to the ETB receptor over the ETA receptor (Kis = 0.023 and 4,200 nM for the rat hippocampal and atrial receptors, respectively).2 It induces contractions in isolated dog saphenous vein segments and relaxation of isolated rabbit mesenteric artery segments in a concentration-dependent manner.3 It increases diastolic arterial pressure in pithed rats when administered at doses ranging from 0.01 to 3 nmol/kg.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1.  .

    2.  .

    3.  .