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Ramorelix

Catalog No.: A60669
LHRH Antagonist
Ramorelix is an LHRH antagonist that inhibits the action of luteinizing hormone, thereby interfering with hormone-driven tumor progression. This compound is primarily utilized in cancer research focused on hormone-sensitive tumors, offering insights into therapeutic strategies targeting the endocrine system. Ramorelix's biological activity makes it a valuable tool for exploring mechanisms of tumor inhibition and advancing anti-cancer therapies.
Ramorelix 127932-90-5 LHRH Antagonist
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Size Price Stock Qty
25mg
$1,275.00
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Research use only. We do not sell to patients.
Data Sheet SDS Compound Handling Instructions

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionRamorelix is an LHRH antagonist that inhibits the action of luteinizing hormone, thereby interfering with hormone-driven tumor progression. This compound is primarily utilized in cancer research focused on hormone-sensitive tumors, offering insights into therapeutic strategies targeting the endocrine system. Ramorelix's biological activity makes it a valuable tool for exploring mechanisms of tumor inhibition and advancing anti-cancer therapies.
Product Information
Catalog NumA60669
FormulaC74H95ClN16O18
Molecular Weight1532.10
CAS Number127932-90-5
Sequence{d-Ala(N-acetyl-3-(2-naphthalenyl))}-{d-Phe(Cl)}-{d-Trp}-Ser-Tyr-{d-Ser(2-(aminocarbonyl)hydrazide)}-Leu-Arg-Pro
Sequence shortening{d-Ala(N-acetyl-3-(2-naphthalenyl))}-{d-Phe(Cl)}-{d-Trp}-SY-{d-Ser(2-(aminocarbonyl)hydrazide)}-LRP
SMILESC([C@@H](NC([C@@H](CC1=CC=C(Cl)C=C1)NC([C@@H](CC2=CC3=C(C=C2)C=CC=C3)NC(C)=O)=O)=O)C(N[C@H](C(N[C@@H](CC4=CC=C(O)C=C4)C(N[C@H](CO[C@H]5[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)C(N[C@H](C(N[C@H](C(=O)N6[C@H](C(NNC(N)=O)=O)CCC6)CCCNC(=N)N)=O)CC(C)C)=O)=O)=O)CO)=O)C=7C=8C(NC7)=CC=CC8
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Endocrinology-Hormones > GnRH receptor