41 Results for "

MEN 4

" in MedChemExpress (MCE) Product Catalog:
Products (41)

41 Results for "MEN 4" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-10199A
CAS No.: 159634-47-6
Purity:  98.52%
Synonyms: MK-677 free base; MK-0677 free base
Ibutamoren (MK-677 free base; MK-0677 free base) is an orally active non-peptide growth hormone secretagogue receptor agonist. Ibutamoren activates signal cascades by mimicking endogenous ligands, triggers pulsatile release of growth hormone from the pituitary gland, and increases serum levels of IGF-1 and insulin-like growth factor-binding protein 3. Ibutamoren not only increases the frequency of growth hormone pulses in male individuals, but also promotes elevated bone formation markers in female individuals with postmenopausal osteoporosis. The combination of Ibutamoren with Alendronate sodium hydrate (HY-11101) significantly increases bone mineral density at the femoral neck. However, Ibutamoren may cause mild, reversible adverse reactions such as increased appetite, fluid retention, and elevated fasting blood glucose. Ibutamoren has been widely used in studies related to idiopathic growth hormone deficiency, sarcopenia, Alzheimer's disease, and osteoporosis .
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1
1 Cited Publications
Cat. No.: HY-151413
CAS No.: 126050-12-2
Purity:  99.69%
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease

MEN 10207 is a selective NK-2 tachykinin receptor (Neurokinin Receptor) antagonist. MEN 10207 has pA2 values of 5.2, 7.9 and 4.9 in three monoreceptor in vitro assays for NK-1, NK-2 and NK-3 tachykinin receptors, respectively.
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1
1 Cited Publications
Cat. No.: HY-P1276A
Synonyms: Neurokinin-2 receptor antagonist TFA
Target:  

Neurokinin Receptor

Research Areas:  

Endocrinology

Men 10376 TFA is a selective tachykinin NK-2 receptor antagonist, with a Ki of 4.4 μM for rat small intestine NK-2 receptor .
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Cat. No.: HY-151595
CAS No.: 2851841-61-5
Purity:  99.85%
Research Areas:  

Cancer

Menin-MLL inhibitor-22 (compound C20) is an orally active inhibitor of the interaction between menin and mixed lineage leukemia (MLL) (IC50=7 nM). Menin-MLL inhibitor-22 binds menin protein and inhibits cancer cell growth (MV4 cells, IC50=0.3 μM). Menin is a putative tumor suppressor associated with multiple endocrine neoplasia type 1 (MEN-1 syndrome) .
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Cat. No.: HY-P1031
CAS No.: 122063-01-8
Synonyms: MEN 10210
Target:  

Neurokinin Receptor

Research Areas:  

Endocrinology

[bAla8]-Neurokinin A(4-10) is a neurokinin 2 (NK2) receptor agonist.
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Cat. No.: HY-P991665
Synonyms: OBT357NF; OBT357

Research Areas:  

Cancer

MEN1112 (OBT357NF; OBT357) is a defucosylated humanized monoclonal antibody targeting Bst1/CD157, with an EC50 of 0.4 nM. MEN1112 binds to Bst1/CD157 on acute myeloid leukemia cells, triggers slow antigen internalization, induces antibody-dependent cell-mediated cytotoxicity, and mediates the lysis of acute myeloid leukemia cells and blasts. MEN1112 is applicable for research related to acute myeloid leukemia .
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Cat. No.: HY-103304
CAS No.: 217438-17-0
Target:  

Others

Research Areas:  

Neurological Disease

CGRP antagonist 4 is an antagonist of calcitonin gene-related peptide (CGRP) receptor. CGRP antagonist 4 shows the highest affinity for CGRP receptors in the human brain. CGRP antagonist 4 can be used to study the binding properties of non-peptide calcitonin gene-related peptide (CGRP) receptor antagonist (gepants) in rat, pig and human menes .
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Cat. No.: HY-W142023
CAS No.: 1047650-51-0
Research Areas:  

Others

(+)-Men-Leu-OH is a leucine derivative .
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Cat. No.: HY-W250654
CAS No.: 1628679-52-6
Target:  

PROTAC Linkers

Research Areas:  

Cancer

PEG2-MeN-Boc is a PROTAC linker that can be used in the synthesis of PROTACs.
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Cat. No.: HY-19395
CAS No.: 197506-04-0
Target:  

Leukotriene Receptor

Research Areas:  

Inflammation/Immunology

MEN-91507 is an orally activecysteinyl leukotriene receptor 1 (CysLTR1) receptor antagonist. MEN-91507 behaves as insurmountable antagonist of Leukotriene D4 (HY-113456)-induced calcium transients, with a pKb of 10.25. MEN-91507 can inhibit Leukotriene D4-induced bronchoconstriction and microvascular leakage in guinea-pigs. MEN-91507 can be used for the researches of inflammation, immunology .
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Cat. No.: HY-151413A
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease

MEN 10207 (acetate) is a selective antagonist of the NK-2 tachykinin receptor. MEN 10207 (acetate) induces tachykinin-induced contractions in rat bladder and guinea pig airways in vivo. MEN 10207 (acetate) inhibits [β-Ala 8 ]-NKA (4-10)-induced enhancement of bladder motility in anesthetized rats and [β-Ala 8 ]-NKA (4-10)-induced enhancement of bronchoconstriction in anesthetized guinea pigs .
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Cat. No.: HY-U00207
CAS No.: 214487-46-4
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease Endocrinology

MEN11467 is a selective and orally- effective peptidomimetic tachykinin NK1 receptor antagonist.
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Cat. No.: HY-P1276
CAS No.: 135306-85-3
Synonyms: Neurokinin-2 receptor antagonist
Target:  

Neurokinin Receptor

Research Areas:  

Endocrinology

Men 10376 is a selective tachykinin NK-2 receptor antagonist, with a Ki of 4.4 μM for rat small intestine NK-2 receptor.
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Cat. No.: HY-W369104
CAS No.: 1338075-62-9
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Boc-MeN-C5-OH is a PROTAC linker that can be used in the synthesis of PROTACs.
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Cat. No.: HY-13745
CAS No.: 211100-13-9
Synonyms: MEN 10755
Sabarubicin (MEN 10755) is a disaccharide analog of Doxorubicin (HY-15142A). Sabarubicin stimulates topoisomerase II-mediated DNA cleavage, induces DNA strand breaks and Apoptosis. Sabarubicin binds to and stabilizes telomeric G-quadruplex DNA. Sabarubicin is applicable to research related to ovarian tumors, breast cancer and lung cancer [4].
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Cat. No.: HY-106277A
CAS No.: 869880-33-1
Synonyms: MEN16132
Target:  

Bradykinin Receptor

Research Areas:  

Metabolic Disease

Fasitibant chloride hydrochloride (MEN16132) is a potent, selective, high affinity, and long-lasting nonpeptide bradykinin B2 (BK2) receptor antagonist. Fasitibant chloride hydrochloride has proinflammatory effects and can be used for the research of osteoarthritis and rheumatoid arthritis .
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Cat. No.: HY-123316
CAS No.: 136949-58-1
Synonyms: Xenetix
Research Areas:  

Others

Iobitridol (Xenetix) is a contrast agent with a higher incidence of adverse reactions in women than in men.
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Cat. No.: HY-103289
CAS No.: 235082-52-7
Purity:  99.15%
MEN 11270, a cyclic decapeptide, is a B2 kinin receptor antagonist. MEN 11270 bound with high-affinity to the B2 kinin receptor constitutively expressed by WI38 human fibroblasts, inhibiting 3H-bradykinin (BK) with a pKi value of 10.3 .
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Cat. No.: HY-14770
CAS No.: 522664-63-7
Synonyms: MEN 15596
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease Endocrinology

Ibodutant (MEN 15596) is a potent and selective tachykinin NK2 receptor antagonist with a pKi of 10.1.
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Cat. No.: HY-P2439
CAS No.: 129781-07-3
Target:  

Neurokinin Receptor

Research Areas:  

Others

MEN 10208 is a neurokinin A antagonist prepared by solid phase synthesis. The Fmoc strategy has more advantages than the Boc strategy in its preparation, and can obtain products with higher yield and purity.
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