35 Results for "

uterus

" in MedChemExpress (MCE) Product Catalog:
Products (35)

35 Results for "uterus" in MCE Product Catalog:

21
21 Publications Verification
Cat. No.: HY-13738
CAS No.: 84449-90-1
Purity:  99.62%
Synonyms: Keoxifene; LY156758 free base; LY139481
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Raloxifene (Keoxifene) is a benzothiophene-derived selective estrogen receptor modulator (SERM). Raloxifene has estrogen-agonistic effects on bone and lipids and estrogen-antagonistic effects on the breast and uterus. Raloxifene is used for breast cancer and osteoporosis research .
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9
9 Cited Publications
Cat. No.: HY-108677
CAS No.: 160312-62-9
Purity:  99.36%
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

L-368,899 hydrochloride is a potent, selective, orally bioavailable, non-peptide oxytocin receptor antagonist, with IC50s of 8.9 nM and 26 nM for rat uterus and human uterus oxytocin receptor, respectively. L-368,899 hydrochloride used as a tocolytic agent .
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2
2 Cited Publications
Cat. No.: HY-119437
CAS No.: 1481401-71-1
Purity:  99.75%
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

FLTX1 is a fluorescent Tamoxifen derivative that can specifically label intracellular Tamoxifen-binding sites (estrogen receptors) under permeabilized and non-permeabilized conditions. FLTX1 exhibits the potent antiestrogenic properties of Tamoxifen in breast cancer cells. FLTX1 is devoid of the estrogenic agonistic effect on the uterus .
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2
2 Cited Publications
Cat. No.: HY-16023
CAS No.: 252555-01-4
Synonyms: EM-652 hydrochloride; SCH 57068 hydrochloride
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

Acolbifene (EM-652) hydrochloride, an active metabolite of EM800, is an orally active, cancer-preventing selective estrogen receptor modulator (SERM). Acolbifene (EM-652) hydrochloride inhibits estradiol (E2)-induced transcriptional activity of ERα (IC50=2 nM) and ERβ (IC50=0.4 nM). Acolbifene (EM-652) hydrochloride exerts a potent and pure antiestrogenic action in the mammary gland and uterus. Anticarcinogenic properties .
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Cat. No.: HY-A0195
CAS No.: 58551-69-2
Research Areas:  

Endocrinology

Carboprost tromethamine is the synthetic 15-methyl analogue of prostaglandin F2α. Carboprost tromethamine can effectively promote law contraction of the uterus and significantly reduce the amount of bleeding during and after delivery .
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Cat. No.: HY-113735
CAS No.: 97468-37-6
Purity:  ≥98.0%
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Cephapirin hemibenzathine is an intrauterine-administered, long-acting cephalosporin antibiotic suitable for the anaerobic environment of the postpartum uterus. Cephapirin hemibenzathine effectively improves the recovery of postpartum buffaloes with subclinical endometritis (SCE) and enhances their reproductive performance. Cephapirin hemibenzathine can be used for the study of subclinical endometritis in postpartum buffaloes .
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Cat. No.: HY-B1403
CAS No.: 84-17-3
Target:  

Estrogen Receptor/ERR

Research Areas:  

Endocrinology

Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge .
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Cat. No.: HY-103283
CAS No.: 81608-30-2
Purity:  98.29%
Synonyms: GRP(18-27) (porcine)
Research Areas:  

Neurological Disease

Neuromedin C porcine (GRP, 18-27, porcine) is a bombesin-like neuropeptide that can be obtained from porcine spinal cord. Neuromedin C porcine exhibits a potent contractile activity on rat uterus in the characteristic manner of bombesin. Neuromedin C porcine has research potential for neurological-related diseases .
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Cat. No.: HY-15008
CAS No.: 148927-60-0
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

L-368,899 is an orally active and selective OT (oxytocin ) receptor antagonist, with IC50s of 8.9 and 26 nM for uterus of rat and human, respectively. L-368,899 can cross the blood-brain barrier (BBB). L-368,899 inhibits oxytocin-stimulated uterine contractions in rats and can be used in study of preterm labor .
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Cat. No.: HY-124114
CAS No.: 110503-62-3
Synonyms: 4-OH-TOR
Target:  

Estrogen Receptor/ERR

Research Areas:  

Endocrinology

4-Hydroxytoremifene (4-OH-TOR) is an estrogen receptor antagonist that blocks the uterus's ability to absorb estradiol .
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Cat. No.: HY-106751
CAS No.: 56470-64-5
Target:  

Progesterone Receptor

Research Areas:  

Endocrinology

Anordrin is a contraceptive agent. Anordrin exhibits estrogenicites and can induce decrease in serum progesterone levels in rat models. Anordrin inhibits endometrial epithelial cell mitosis and NAFLD induced by Tamoxifen (HY-13757A) in mouse uterus and liver as an anti-estrogenic and estrogenic agent .
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Cat. No.: HY-P1767
CAS No.: 111366-38-2
Target:  

PACAP Receptor

Research Areas:  

Cardiovascular Disease

Prepro VIP (81-122), human is a prepro-vasoactive intestinal polypeptide (VIP) derived peptide, corresponding to residues 81-122. Peptide histidine valine 42 (PHV-42) has been designated to correspond exactly to Prepro VIP (81-122), which reduces both the force and frequency of spontaneous contractions of isolated rat uterus .
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Cat. No.: HY-129278
CAS No.: 24185-51-1
Lunarine is an alkaloid, which can be isolated from the seeds of kale (Lunaria annua). Lunarine lowers the blood pressure, stimulates small intestinal motility, inhibits spontaneous contractions of uterus and nervous system, and exhibits an acute toxicity with LD50 of 62.3 mg/kg in dogs and rabbits. Lunarine exhibits antiparasitic activity through a competitive inhibition of protozoan oxidoreductase trypanothione reductase (TryR) with Ki of 304 μM .
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Cat. No.: HY-B1403S
CAS No.: 1346606-45-8
Dienestrol-d2 is a deuterium labeled Dienestrol (HY-B1403). Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge .
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Cat. No.: HY-B1403R
CAS No.: 84-17-3
Dienestrol (Standard) is the analytical standard of Dienestrol (HY-B1403). This product is intended for research and analytical applications. Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge .
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Cat. No.: HY-13738S2
CAS No.: 1188263-47-9
Raloxifene-d4 (hydrochloride) is the deuterium labeled Raloxifene. Raloxifene (Keoxifene) is a benzothiophene-derived selective estrogen receptor modulator (SERM). Raloxifene has estrogen-agonistic effects on bone and lipids and estrogen-antagonistic effects on the breast and uterus. Raloxifene is used for breast cancer and osteoporosis research .
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Cat. No.: HY-13738S
CAS No.: 1185076-44-1
Raloxifene-d4 is the deuterium labeled Raloxifene. Raloxifene (Keoxifene) is a benzothiophene-derived selective estrogen receptor modulator (SERM). Raloxifene has estrogen-agonistic effects on bone and lipids and estrogen-antagonistic effects on the breast and uterus. Raloxifene is used for breast cancer and osteoporosis research .
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Cat. No.: HY-13738S3
CAS No.: 2512224-37-0
Raloxifene-d10 is the deuterium labeled Raloxifene. Raloxifene (Keoxifene) is a benzothiophene-derived selective estrogen receptor modulator (SERM). Raloxifene has estrogen-agonistic effects on bone and lipids and estrogen-antagonistic effects on the breast and uterus. Raloxifene is used for breast cancer and osteoporosis research .
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Cat. No.: HY-13738R
CAS No.: 84449-90-1
Synonyms: Keoxifene (Standard); LY156758 free base (Standard); LY139481 (Standard)
Research Areas:  

Cancer

Raloxifene (Standard) is the analytical standard of Raloxifene. This product is intended for research and analytical applications. Raloxifene (Keoxifene) is a benzothiophene-derived selective estrogen receptor modulator (SERM). Raloxifene has estrogen-agonistic effects on bone and lipids and estrogen-antagonistic effects on the breast and uterus. Raloxifene is used for breast cancer and osteoporosis research .
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Cat. No.: HY-A0195R
CAS No.: 58551-69-2
Research Areas:  

Endocrinology

Carboprost (tromethamine) (Standard) is the analytical standard of Carboprost (tromethamine). This product is intended for research and analytical applications. Carboprost tromethamine is the synthetic 15-methyl analogue of prostaglandin F2α. Carboprost tromethamine can effectively promote law contraction of the uterus and significantly reduce the amount of bleeding during and after delivery .
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