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Intraperitoneal Administration Equipment & Supplies

81 equipment items found

MedChemExpress - Model LP44 hydrochloride - 824958-12-5

MedChemExpress - Model LP44 hydrochloride - 824958-12-5

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
LP44 (hydrochloride) induces hypothermic effect in a dose-dependent manner by intracerebroventricular injection. LP44 (hydrochloride) not causes considerable hypothermic response by intraperitoneal ...
CONTACT SUPPLIER

MedChemExpress - Model VPC-70619 - 2361742-30-3

MedChemExpress - Model VPC-70619 - 2361742-30-3

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
VPC-70619 blocks the N-Myc-Max heterocomplex from binding to DNA E-boxes and demonstrated strong inhibition activity against N-Myc-dependent cell lines as well as high bioavailability in both oral and intraperitoneal ...
CONTACT SUPPLIER

MedChemExpress - Model A924 - 65132-74-3

MedChemExpress - Model A924 - 65132-74-3

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
A 924 is an amino acid derivative-based, orally active antitumor agent. A 924 is effective in inhibiting ascites tumors in rat models by intraperitoneal injection or oral administration. The LD50 of A 924 in mice is >1.5 g/kg and >4.5 g/kg by intraperitoneal injection or oral administration, respectively. A 924 does not cause ...
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MedChemExpress - Model (-)-JM-1232 - 1013427-48-9

MedChemExpress - Model (-)-JM-1232 - 1013427-48-9

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
(-)-JM-1232 (MR04A3) targets GABA A receptors and exerts its analgesic effects by binding to the benzodiazepine binding site of GABA A receptors. (-)-JM-1232 demonstrates potent analgesic effects in mice against acute thermal stimuli, mechanically induced pain, and visceral pain, with CI50 values of 2.96, 3.06, and 2.27 mg/kg, respectively. (-)-JM-1232 can be used in research related to pain and ...
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MedChemExpress - Model Alniditan dihydrochloride - 155428-00-5

MedChemExpress - Model Alniditan dihydrochloride - 155428-00-5

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Alniditan (Alnitidan) dihydrochloride is a potent 5-HT1B and 5-HT1D receptors agonist, with IC50s of 1.7 nM and 1.3 nM for h5-HT1B and h5-HT1D receptors in HEK?293 cells, respectively. Alniditan dihydrochloride has migraine-preventive ...
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MedChemExpress - Model (R)-Baclofen - 69308-37-8

MedChemExpress - Model (R)-Baclofen - 69308-37-8

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
(R)-Baclofen (Arbaclofen) is a selective GABAB receptor ...
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MedChemExpress - Model ACHN-975 TFA - 1410809-37-8

MedChemExpress - Model ACHN-975 TFA - 1410809-37-8

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
ACHN-975 TFA is a selective LpxC inhibitor and exhibits a subnanomolar LpxC inhibitory activity. ACHN-975 TFA is against a wide range of gram-negative bacterias with low MIC values (≤1 ...
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MedChemExpress - Model Poncirin - 14941-08-3

MedChemExpress - Model Poncirin - 14941-08-3

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Poncirin is isolated from?Poncirus trifoliata with anti-inflammory activites. Poncirin significantly reduces mechanical hyperalgesia and allodynia in Complete Freund’s Adjuvant (CFA)-induced inflammatory pain ...
CONTACT SUPPLIER

MedChemExpress - Model 7ACC2 - 1472624-85-3

MedChemExpress - Model 7ACC2 - 1472624-85-3

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
7ACC2 is a potent monocarboxylate transporter (MCT) inhibitor with an IC50 of 11 nM for inhibition of [14C]-lactate influx. 7ACC2 is also a potent inhibitor of mitochondrial pyruvate transport. 7ACC2 is an anticancer agent through inhibition of lactate ...
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MedChemExpress - Model URB-597 - 546141-08-6

MedChemExpress - Model URB-597 - 546141-08-6

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
URB-597 (KDS-4103) is an orally bioavailable and selective FAAH inhibitor. URB-597 inhibits FAAH activity with an IC50s of approximately 5 nM in rat brain membranes, 0.5 nM in intact rat neurons, 3 nM in human liver microsomes. Antidepressant-like effects. Analgesic ...
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MedChemExpress - Model EMD534085 - 858668-07-2

MedChemExpress - Model EMD534085 - 858668-07-2

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
EMD534085 is a potent and selective inhibitor of the mitotic kinesin-5 with an IC50 of 8 nM. ...
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MedChemExpress - Model Metoprine - 7761-45-7

MedChemExpress - Model Metoprine - 7761-45-7

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Metoprine (BW 197U) is a potent histamine N-methyltransferase (HMT) inhibitor. Metoprine, a diaminopyrimidine derivative, can cross the blood-brain barrier and increase brain histamine levels by inhibiting HMT[1][2]. Metoprine is an antifolate and antitumor ...
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MedChemExpress - Model 1-Naphthohydroxamic acid - 6953-61-3

MedChemExpress - Model 1-Naphthohydroxamic acid - 6953-61-3

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
1-Naphthohydroxamic acid (Compound 2) is a potent and selective HDAC8 inhibitor with an IC50 of 14 μM. 1-Naphthohydroxamic acid is more selectively for HDAC8 than class I HDAC1 and class II HDAC6 (IC50 >100 μM). 1-Naphthohydroxamic acid does not increase global histone H4 acetylation and also does not reduce total intracellular HDAC activity[1][2].1-Naphthohydroxamic acid can induce tubulin ...
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MedChemExpress - Model (R)-Baclofen hydrochloride - 63701-55-3

MedChemExpress - Model (R)-Baclofen hydrochloride - 63701-55-3

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
(R)-Baclofen hydrochloride (Arbaclofen hydrochloride) is a selective GABAB receptor ...
CONTACT SUPPLIER

MedChemExpress - Model Mal-amido-PEG2-C2-amido-Ph-C2-CO-AZD - 1037589-69-7

MedChemExpress - Model Mal-amido-PEG2-C2-amido-Ph-C2-CO-AZD - 1037589-69-7

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Mal-amido-PEG2-C2-amido-Ph-C2-CO-AZD (Mal-PEG2-AZD) is a PEG-based PROTAC linker that can be used in the synthesis of ...
CONTACT SUPPLIER

MedChemExpress - Model Dimethocaine - 94-15-5

MedChemExpress - Model Dimethocaine - 94-15-5

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Dimethocaine (Larocaine) can alleviate pain and sensation by blocking the sodium ion channels inside ...
CONTACT SUPPLIER

MedChemExpress - Model DJ-V-159 - 2253744-53-3

MedChemExpress - Model DJ-V-159 - 2253744-53-3

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
DJ-V-159 is an agonist for G protein-coupled receptor family C group 6 member A ...
CONTACT SUPPLIER

MedChemExpress - Model Mepazine hydrochloride - 2975-36-2

MedChemExpress - Model Mepazine hydrochloride - 2975-36-2

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Mepazine hydrochloride (Pecazine hydrochloride) is a potent and selective MALT1 protease inhibitor with IC50s of 0.83 and 0.42 μM for GSTMALT1 full length and GSTMALT1 325-760, respectively. Mepazine hydrochloride affects viability of ABC-DLBCL cells by enhancing ...
CONTACT SUPPLIER

MedChemExpress - Model Mepazine - 60-89-9

MedChemExpress - Model Mepazine - 60-89-9

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Mepazine (Pecazine) is a potent and selective MALT1 protease inhibitor with IC50s of 0.83 and 0.42 μM for GSTMALT1 full length and GSTMALT1 325-760, respectively. Mepazine affects viability of ABC-DLBCL cells by enhancing ...
CONTACT SUPPLIER

MedChemExpress - Model Aplaviroc hydrochloride - 461023-63-2

MedChemExpress - Model Aplaviroc hydrochloride - 461023-63-2

Manufactured by:MedChemExpress LLC (MCE)   based inMonmouth Junction, NEW JERSEY (USA)
Aplaviroc (AK 602) hydrochloride, a SDP derivative, is a CCR5 antagonist, with IC50s of 0.1-0.4 nM for HIV-1Ba-L, HIV-1JRFL and ...
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