hae

HAE (His-Ala-Glu) consists of histidine, alanine and glutamate.

HAE acetate is a 3-amino acid peptide composed of histidine, alanine and glutamate

HAEGTFTSDVSSYLE is a peptide. GLP-I analog contains the sequence.

Haemanthamine is an alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. It inhibits protein biosynthesis during the elongation stage of translation. It has antimalarial, pro-apoptotic, antiviral, antioxidant, and anticonvulsa

Haemanthamine hydrochloride is an alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. It inhibits protein biosynthesis during the elongation stage of translation. It has antimalarial, pro-apoptotic, antiviral, antioxidant, an

Cephaeline dihydrobromide is a useful organic compound for research related to life sciences and the catalog number is T124574.

Chaetopenoid B is a useful organic compound for research related to life sciences. The catalog number is T125487 and the CAS number is 1893386-00-9.

Chaetopenoid A is a useful organic compound for research related to life sciences. The catalog number is T125488 and the CAS number is 1893385-99-3.

Sphaerobioside is a useful organic compound for research related to life sciences. The catalog number is T125786 and the CAS number is 14988-20-6.

19-O-Acetylchaetoglobosin D is a useful organic compound for research related to life sciences and the catalog number is T129448.

Sphaerindicin is a useful organic compound for research related to life sciences and the catalog number is T130184.

Chaetoglobosin A, the active compound extracted of Penicillium aquamarinium, is a member of the cytochalasan family. It preferentially induces apoptosis.

Chaetominine is a type of cytotoxic alkaloid obtained from endophytic Chaetomium sp. IFB-E015.

Sphaeropsidin A is the main phytotoxin produced by Diplodia cupressi.

Sphaeropsidin B is a fungal phytotoxin.

19-O-Acetylchaetoglobosin A is a fungal metabolite originally isolated fromC. globosumthat has actin polymerization inhibitory and cytotoxic activities.1,2It inhibits actin polymerization in a cell-free assay when used at a concentration of 2 μM.219-O-Acetylchaetoglobosin A (3.2, 10, and 32 μg/ml) is cytotoxic to HeLa cervical cancer cells.1 1.Umeda, M., Ohtsubo, K., Saito, M., et al.Cytotoxicity of new cytochalasans from Chaetomium globosumExperientia31(4)435-438(1975) 2.Sekita, S., Yoshihira, K., Natori, S., et al.Structure-activity relationship of thirty-nine cytochalasans observed in the effects on cellular structures and cellular events and on actin polymerization in vitroJ. Pharmacobiodyn.8(11)906-916(1985)

Cephaeline hydrochloride, a phenolic alkaloid found in Indian Ipecac, effectively inhibits the infection of viruses ZIKV and EBOV.

Chaetocin, a natural product from Chaetomium species, is a histone methyltransferase inhibitor with IC50 of 0.8 μM, 2.5 μM and 3 μM for dSU(VAR)3-9, mouse G9a and Neurospora crassa DIM5, respectively.

Chaetochromin also known as 4548-G05 and NSC 345647, is an orally active, small-molecule, selective agonist of the insulin receptor. It has potent and long-lasting antidiabetic activity in vivo in mice.

Chaetomellic acid A is a potent inhibitor of farnesyltransferase in isolated enzyme assays (IC50=55nM) but is inactive in whole cells. Inhibition of farnesyltransferase is selective over geranylgeranyltransferase I and II (IC50=92µM and 34µM respectively).

Chaetochromin C also known as 4548-G05, is an orally active, small-molecule, selective agonist of the insulin receptor.

Chaetochromin D also known as 4548-G05, is an orally active, small-molecule, selective agonist of the insulin receptor.

Haemanthamine hydrochloride, a crinine-type alkaloid derived from Amaryllidaceae plants, exhibits potent anticancer properties. It acts by targeting ribosomes, thereby inhibiting protein biosynthesis during the translation elongation stage. Additionally, this compound demonstrates pro-apoptotic, antioxidant, antiviral, antimalarial, and anticonvulsant activities [1] [2].

11-epi-Chaetomugilin I, a metabolite identified in Chaetomium globosum, demonstrates notable cytotoxic activity against several cell lines, including the murine P388 and L1210 leukemia cell lines, the human HL-60 leukemia cell line, and the human KB epidermoid carcinoma cell line [1].