Molecules

Name	Type	Specific against	Appl.	Item no.	Amount	Price
4SC-202	Inhibitors	Other		DCC-DC7592-250mg DCChemicals	250 mg	Login Compare	4SC-202
VE-822 (Berzosertib)	Inhibitors	Other		DCC-DC7527-1g DCChemicals	1 g	Login Compare	VE-822 (Berzosertib)
4SC-202	Inhibitors	Other		DCC-DC7592-1g DCChemicals	1 g	Login Compare	4SC-202
LIPID A6	Chemicals	Other	ELISA, other, IV	DCC-DC80050-25mg DCChemicals	25 mg	Login Compare	LIPID A6
Zinc protoporphyrin	Chemicals	Other	Zinc Protoporphyrin (Zn(II)-protoporphyrin IX) is an orally active and competitive heme oxygenase-1 (HO-1) inhibitor and markedly attenuates the protective effects of Phloroglucinol (PG) against H2O2[1]. Zinc Protoporphyrin is used as a screening marker o, but also to assess population iron status in combination with haemoglobin concentration[2]. Zinc Protoporphyrin has anti-cancer activity[3].	DCC-DC80075-25mg DCChemicals	25 mg	Login Compare	Zinc protoporphyrin
113-O12B	Chemicals	Other	other	DCC-DC80065-25mg DCChemicals	25 mg	Login Compare	113-O12B
OF-C4-Deg-Lin	Chemicals	Other	ELISA, other	DCC-DC80080-25mg DCChemicals	25 mg	Login Compare	OF-C4-Deg-Lin
Azido-PEG4-EV-Cit-PAB-MMAE	Chemicals	Other	Azido-PEG4-EV-Cit-PAB-MMAE is a precursor of antibody drug conjugate.	DCC-DC80073-10mg DCChemicals	10 mg	Login Compare	Azido-PEG4-EV-Cit-PAB-MMAE
A18-ISO5-2DC18 (Pimidol)	Chemicals	Other		DCC-DC80071-25mg DCChemicals	25 mg	Login Compare	A18-ISO5-2DC18 (Pimidol)
p-Tolyl-β-D-glucuronide	Chemicals	Other	p-Cresol glucuronide is a metabolite of p-cresol, a uremic toxin formed by bacterial fermentation of proteins in the large intestine. It is formed from p-cresol primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT1A6, but also by UGT1A9, in human liver and kidney microsomes. p-Cresol glucuronide accumulates in feces, blood, and urine of patients with chronic kidney disease (CKD).	DCC-DC80060-100mg DCChemicals	100 mg	Login Compare	p-Tolyl-β-D-glucuronide
p-Tolyl-β-D-glucuronide	Chemicals	Other	p-Cresol glucuronide is a metabolite of p-cresol, a uremic toxin formed by bacterial fermentation of proteins in the large intestine. It is formed from p-cresol primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT1A6, but also by UGT1A9, in human liver and kidney microsomes. p-Cresol glucuronide accumulates in feces, blood, and urine of patients with chronic kidney disease (CKD).	DCC-DC80060-250mg DCChemicals	250 mg	Login Compare	p-Tolyl-β-D-glucuronide
p-Tolyl-β-D-glucuronide	Chemicals	Other	p-Cresol glucuronide is a metabolite of p-cresol, a uremic toxin formed by bacterial fermentation of proteins in the large intestine. It is formed from p-cresol primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT1A6, but also by UGT1A9, in human liver and kidney microsomes. p-Cresol glucuronide accumulates in feces, blood, and urine of patients with chronic kidney disease (CKD).	DCC-DC80060-1g DCChemicals	1 g	Login Compare	p-Tolyl-β-D-glucuronide
306Oi10	Chemicals	Other	306Oi10 is a branched-chain ionizable lipidoid and may be useful in the generation of lipid nanoparticles (LNPs).	DCC-DC80066-100mg DCChemicals	100 mg	Login Compare	306Oi10
H-D-Pro-Phe-Arg-pNA·2 HCl	Chemicals	Other	S-2302 is a Chromogenic substrate for plasma kallikrein, factor XIa and factor XIIa.	DCC-DC80052-100mg DCChemicals	100 mg	Login Compare	H-D-Pro-Phe-Arg-pNA·2 HCl
H-D-Pro-Phe-Arg-pNA·2 HCl	Chemicals	Other	S-2302 is a Chromogenic substrate for plasma kallikrein, factor XIa and factor XIIa.	DCC-DC80052-250mg DCChemicals	250 mg	Login Compare	H-D-Pro-Phe-Arg-pNA·2 HCl
H-D-Pro-Phe-Arg-pNA·2 HCl	Chemicals	Other	S-2302 is a Chromogenic substrate for plasma kallikrein, factor XIa and factor XIIa.	DCC-DC80052-1g DCChemicals	1 g	Login Compare	H-D-Pro-Phe-Arg-pNA·2 HCl
ZINC36395841(compound 25)	Chemicals	Other		DCC-DC80036-10mg DCChemicals	10 mg	Login Compare	ZINC36395841(compound 25)
WAY-647802	Chemicals	Other	WAY-647802 is a CDK inhibitor.	DCC-DC80035-100mg DCChemicals	100 mg	Login Compare	WAY-647802
WAY-647802	Chemicals	Other	WAY-647802 is a CDK inhibitor.	DCC-DC80035-250mg DCChemicals	250 mg	Login Compare	WAY-647802
WAY-647802	Chemicals	Other	WAY-647802 is a CDK inhibitor.	DCC-DC80035-1g DCChemicals	1 g	Login Compare	WAY-647802
DSPE-PEG2000-DBCO	Chemicals	Other	Cu-free click chemistry with readily synthesized biarylazacyclooctynones. The reaction of azides with strained alkynes, such as cyclooctynes, readily forms a triazole product without the need for a toxic catalyst.	DCC-DC80023-100mg DCChemicals	100 mg	Login Compare	DSPE-PEG2000-DBCO
VV116	Chemicals	Other	VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SARS-CoV-2. VV116 is a deuterated, tri-isobutyrate ester prodrug of the RDV parent nucleoside, and is rapidly metabolized into the parent nucleoside (116-N1) in the body. 116-N1 is intracellularly converted to the nucleoside triphosphate active form, which would interfere with the function of RNA-dependent RNA polymerase of SARS-CoV-2, thus exerting antiviral effects (Fig. 1). VV116 showed potent activity against a panel of SARS-CoV-2 variants (alpha, beta, delta, and omicron) and excellent therapeutic efficacy in the mice model.	DCC-DC80018-10mg DCChemicals	10 mg	Login Compare	VV116
VV116	Chemicals	Other	VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SARS-CoV-2. VV116 is a deuterated, tri-isobutyrate ester prodrug of the RDV parent nucleoside, and is rapidly metabolized into the parent nucleoside (116-N1) in the body. 116-N1 is intracellularly converted to the nucleoside triphosphate active form, which would interfere with the function of RNA-dependent RNA polymerase of SARS-CoV-2, thus exerting antiviral effects (Fig. 1). VV116 showed potent activity against a panel of SARS-CoV-2 variants (alpha, beta, delta, and omicron) and excellent therapeutic efficacy in the mice model.	DCC-DC80018-25mg DCChemicals	25 mg	Login Compare	VV116
VV116	Chemicals	Other	VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SARS-CoV-2. VV116 is a deuterated, tri-isobutyrate ester prodrug of the RDV parent nucleoside, and is rapidly metabolized into the parent nucleoside (116-N1) in the body. 116-N1 is intracellularly converted to the nucleoside triphosphate active form, which would interfere with the function of RNA-dependent RNA polymerase of SARS-CoV-2, thus exerting antiviral effects (Fig. 1). VV116 showed potent activity against a panel of SARS-CoV-2 variants (alpha, beta, delta, and omicron) and excellent therapeutic efficacy in the mice model.	DCC-DC80018-100mg DCChemicals	100 mg	Login Compare	VV116
Aminopurvalanol A	Chemicals	Other	selective, Aminopurvalanol A is a potent, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of ph	DCC-DC80011-100mg DCChemicals	100 mg	Login Compare	Aminopurvalanol A

Name Price

4SC-202

Type	Inhibitors
Clone
Specific against	Other
Appl.
Host
Item no.	DCC-DC7592-250mg
Amount	250 mg
Available

VE-822 (Berzosertib)

Type	Inhibitors
Clone
Specific against	Other
Appl.
Host
Item no.	DCC-DC7527-1g
Amount	1 g
Available

4SC-202

Type	Inhibitors
Clone
Specific against	Other
Appl.
Host
Item no.	DCC-DC7592-1g
Amount	1 g
Available

LIPID A6

Type	Chemicals
Clone
Specific against	Other
Appl.	ELISA, other, IV
Host
Item no.	DCC-DC80050-25mg
Amount	25 mg
Available

Zinc protoporphyrin

Type	Chemicals
Clone
Specific against	Other
Appl.	Zinc Protoporphyrin (Zn(II)-protoporphyrin IX) is an orally active and competitive heme oxygenase-1 (HO-1) inhibitor and markedly attenuates the protective effects of Phloroglucinol (PG) against H2O2[1]. Zinc Protoporphyrin is used as a screening marker o, but also to assess population iron status in combination with haemoglobin concentration[2]. Zinc Protoporphyrin has anti-cancer activity[3].
Host
Item no.	DCC-DC80075-25mg
Amount	25 mg
Available

113-O12B

Type	Chemicals
Clone
Specific against	Other
Appl.	other
Host
Item no.	DCC-DC80065-25mg
Amount	25 mg
Available

OF-C4-Deg-Lin

Type	Chemicals
Clone
Specific against	Other
Appl.	ELISA, other
Host
Item no.	DCC-DC80080-25mg
Amount	25 mg
Available

Azido-PEG4-EV-Cit-PAB-MMAE

Type	Chemicals
Clone
Specific against	Other
Appl.	Azido-PEG4-EV-Cit-PAB-MMAE is a precursor of antibody drug conjugate.
Host
Item no.	DCC-DC80073-10mg
Amount	10 mg
Available

A18-ISO5-2DC18 (Pimidol)

Type	Chemicals
Clone
Specific against	Other
Appl.
Host
Item no.	DCC-DC80071-25mg
Amount	25 mg
Available

p-Tolyl-β-D-glucuronide

Type	Chemicals
Clone
Specific against	Other
Appl.	p-Cresol glucuronide is a metabolite of p-cresol, a uremic toxin formed by bacterial fermentation of proteins in the large intestine. It is formed from p-cresol primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT1A6, but also by UGT1A9, in human liver and kidney microsomes. p-Cresol glucuronide accumulates in feces, blood, and urine of patients with chronic kidney disease (CKD).
Host
Item no.	DCC-DC80060-100mg
Amount	100 mg
Available

p-Tolyl-β-D-glucuronide

Type	Chemicals
Clone
Specific against	Other
Appl.	p-Cresol glucuronide is a metabolite of p-cresol, a uremic toxin formed by bacterial fermentation of proteins in the large intestine. It is formed from p-cresol primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT1A6, but also by UGT1A9, in human liver and kidney microsomes. p-Cresol glucuronide accumulates in feces, blood, and urine of patients with chronic kidney disease (CKD).
Host
Item no.	DCC-DC80060-250mg
Amount	250 mg
Available

p-Tolyl-β-D-glucuronide

Type	Chemicals
Clone
Specific against	Other
Appl.	p-Cresol glucuronide is a metabolite of p-cresol, a uremic toxin formed by bacterial fermentation of proteins in the large intestine. It is formed from p-cresol primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT1A6, but also by UGT1A9, in human liver and kidney microsomes. p-Cresol glucuronide accumulates in feces, blood, and urine of patients with chronic kidney disease (CKD).
Host
Item no.	DCC-DC80060-1g
Amount	1 g
Available

306Oi10

Type	Chemicals
Clone
Specific against	Other
Appl.	306Oi10 is a branched-chain ionizable lipidoid and may be useful in the generation of lipid nanoparticles (LNPs).
Host
Item no.	DCC-DC80066-100mg
Amount	100 mg
Available

H-D-Pro-Phe-Arg-pNA·2 HCl

Type	Chemicals
Clone
Specific against	Other
Appl.	S-2302 is a Chromogenic substrate for plasma kallikrein, factor XIa and factor XIIa.
Host
Item no.	DCC-DC80052-100mg
Amount	100 mg
Available

H-D-Pro-Phe-Arg-pNA·2 HCl

Type	Chemicals
Clone
Specific against	Other
Appl.	S-2302 is a Chromogenic substrate for plasma kallikrein, factor XIa and factor XIIa.
Host
Item no.	DCC-DC80052-250mg
Amount	250 mg
Available

H-D-Pro-Phe-Arg-pNA·2 HCl

Type	Chemicals
Clone
Specific against	Other
Appl.	S-2302 is a Chromogenic substrate for plasma kallikrein, factor XIa and factor XIIa.
Host
Item no.	DCC-DC80052-1g
Amount	1 g
Available

ZINC36395841(compound 25)

Type	Chemicals
Clone
Specific against	Other
Appl.
Host
Item no.	DCC-DC80036-10mg
Amount	10 mg
Available

WAY-647802

Type	Chemicals
Clone
Specific against	Other
Appl.	WAY-647802 is a CDK inhibitor.
Host
Item no.	DCC-DC80035-100mg
Amount	100 mg
Available

WAY-647802

Type	Chemicals
Clone
Specific against	Other
Appl.	WAY-647802 is a CDK inhibitor.
Host
Item no.	DCC-DC80035-250mg
Amount	250 mg
Available

WAY-647802

Type	Chemicals
Clone
Specific against	Other
Appl.	WAY-647802 is a CDK inhibitor.
Host
Item no.	DCC-DC80035-1g
Amount	1 g
Available

DSPE-PEG2000-DBCO

Type	Chemicals
Clone
Specific against	Other
Appl.	Cu-free click chemistry with readily synthesized biarylazacyclooctynones. The reaction of azides with strained alkynes, such as cyclooctynes, readily forms a triazole product without the need for a toxic catalyst.
Host
Item no.	DCC-DC80023-100mg
Amount	100 mg
Available

VV116

Type	Chemicals
Clone
Specific against	Other
Appl.	VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SARS-CoV-2. VV116 is a deuterated, tri-isobutyrate ester prodrug of the RDV parent nucleoside, and is rapidly metabolized into the parent nucleoside (116-N1) in the body. 116-N1 is intracellularly converted to the nucleoside triphosphate active form, which would interfere with the function of RNA-dependent RNA polymerase of SARS-CoV-2, thus exerting antiviral effects (Fig. 1). VV116 showed potent activity against a panel of SARS-CoV-2 variants (alpha, beta, delta, and omicron) and excellent therapeutic efficacy in the mice model.
Host
Item no.	DCC-DC80018-10mg
Amount	10 mg
Available

VV116

Type	Chemicals
Clone
Specific against	Other
Appl.	VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SARS-CoV-2. VV116 is a deuterated, tri-isobutyrate ester prodrug of the RDV parent nucleoside, and is rapidly metabolized into the parent nucleoside (116-N1) in the body. 116-N1 is intracellularly converted to the nucleoside triphosphate active form, which would interfere with the function of RNA-dependent RNA polymerase of SARS-CoV-2, thus exerting antiviral effects (Fig. 1). VV116 showed potent activity against a panel of SARS-CoV-2 variants (alpha, beta, delta, and omicron) and excellent therapeutic efficacy in the mice model.
Host
Item no.	DCC-DC80018-25mg
Amount	25 mg
Available

VV116

Type	Chemicals
Clone
Specific against	Other
Appl.	VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SARS-CoV-2. VV116 is a deuterated, tri-isobutyrate ester prodrug of the RDV parent nucleoside, and is rapidly metabolized into the parent nucleoside (116-N1) in the body. 116-N1 is intracellularly converted to the nucleoside triphosphate active form, which would interfere with the function of RNA-dependent RNA polymerase of SARS-CoV-2, thus exerting antiviral effects (Fig. 1). VV116 showed potent activity against a panel of SARS-CoV-2 variants (alpha, beta, delta, and omicron) and excellent therapeutic efficacy in the mice model.
Host
Item no.	DCC-DC80018-100mg
Amount	100 mg
Available

Aminopurvalanol A

Type	Chemicals
Clone
Specific against	Other
Appl.	selective, Aminopurvalanol A is a potent, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of ph
Host
Item no.	DCC-DC80011-100mg
Amount	100 mg
Available

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