Caerulein, desulfated TFA (20994-83-6 free base)
CAS No. ——
Caerulein, desulfated TFA (20994-83-6 free base)( —— )
Catalog No. M30076 CAS No. ——
Caerulein, desulfated TFA is Caerulein after desulfurization.Caerulein is a deceptide with the same five carboxy-terminating amino acids as gastrin and cholecystatin (CCK).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameCaerulein, desulfated TFA (20994-83-6 free base)
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NoteResearch use only, not for human use.
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Brief DescriptionCaerulein, desulfated TFA is Caerulein after desulfurization.Caerulein is a deceptide with the same five carboxy-terminating amino acids as gastrin and cholecystatin (CCK).
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DescriptionCaerulein, desulfated TFA is Caerulein after desulfurization.Caerulein is a deceptide with the same five carboxy-terminating amino acids as gastrin and cholecystatin (CCK)..
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number——
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Formula Weight1386.36
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Molecular FormulaC60H74F3N13O20S
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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Chemical NameSequence:{Glp}{Gln}{Asp}{Tyr}{Thr}{Gly}{Trp}{Met}{Asp}{Phe}-NH2
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Cloransulam-methyl
Cloransulam-methyl is an effective herbicide that is often applied to soybean fields to control broadleaf weeds.Cloransulam-methyl is rapidly metabolised in the soybean plant but is present in the soil.CBiPES hydrochloride (CBiPES HCl) is a potent orthosteric modulator of the mGlu2 receptor.
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Methyl stearate
Methyl stearate is found in cloves. Antifoaming agent and fermentation nutrient.
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PAR-3 (1-6) (human)
PAR3 (1-6) is a synthetic peptide agonist of proteinase-activated receptor 1 (PAR1) that corresponds to residues 1-6 of the amino terminal tethered ligand sequence of human PAR3 and residues 39-44 of the full-length human sequence. PAR3 (1-6) activates p42/44 MAPK signaling in fibroblasts expressing PAR1, but not PAR3, an effect that can be blocked by the PAR1 antagonist RWJ 56110.
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