Doxorubicin hydrochloride

Background: Many a long time of analysis demonstrates that the presence of and perceived high quality of the parent-child bond can impression a toddler’s well being, psychological well being, and interpersonal trajectory for a lifetime (Weinfield, Sroufe, Egeland, & Carlson, 1999 Handbook of attachment: Idea, analysis, and medical functions.

Doxorubicin hydrochloride

New York: Guilford Press, 68; Lieberman, Toddler Psychological Well being Journal, 25, 336, 2004). Nevertheless, investigations relating to the utility of strategies to guage the standard and nature of caregiver-child interactions are restricted. Utilizing medical information from 151 caregiver-child dyads, this examine examines the psychometric properties of the Crowell Downside Fixing Process Score Scale utilizing exploratory issue evaluation. Moreover, the predictive validity of the coding system was examined by way of comparisons with the Guardian-Toddler Relationship International Evaluation Scale (PIRGAS).
Findings: The kid and grownup scales had been every psychometrically outlined by a single issue that was internally constant and well-defined conceptually by the consultant gadgets. Excessive inner consistency for every scale supplies help for the reliability of the ranking scale, and means that the Crowell scores might be helpful as two separate scales measuring a toddler’s affective presentation and caregiver responsiveness, but additionally collectively as a complete rating assessing general relational functioning. Facets of the caregiver-child relationship had been considerably associated to PIRGAS scores on the kid and grownup domains.
Conclusions: The outcomes of this examine recommend the Crowell Downside Fixing Process Score Scale is a quick instrument, with good inner consistency, that may assess a variety of younger youngsters, in a medical setting.
Key phrases: Attachment; caregiver; youngster improvement; relationships.

Rising Prevalence of Multidrug-Resistant Candida haemulonii Species Advanced amongst All Yeast Cultures Collected by a Reference Laboratory over the Previous 11 Years

  • There may be worldwide concern with the growing charges of infections attributable to multiresistant Candida isolates reported in tertiary medical facilities. We checked for historic traits when it comes to prevalence charges and antifungal susceptibility of the Candida haemulonii species complicated in our yeast inventory tradition collected over the last 11 years.
  • The isolates had been recognized by sequencing the rDNA inner transcribed spacer (ITS) area, and antifungal susceptibility checks for amphotericin B, voriconazole, fluconazole, anidulafungin, and 5-fluorocytosine had been carried out by the Medical and Laboratory Requirements Institute (CLSI) microbroth methodology. A complete of 49 isolates had been recognized as Candida haemulonii sensu stricto (n = 21), adopted by C.
  • haemulonii var. vulnera (n = 15) and C. duobushaemulonii (n = 13), together with 38 isolates cultured from sufferers with deep-seated Candida infections. The prevalence of the C.

Doxorubicin hydrochloride

GA4969-100MG 100 mg
EUR 181

Doxorubicin hydrochloride

GA4969-10MG 10 mg
EUR 78

Doxorubicin hydrochloride

GA4969-25MG 25 mg
EUR 98

Doxorubicin hydrochloride

GA4969-50MG 50 mg
EUR 126

Doxorubicin hydrochloride USP

D005-10MG 10 mg
EUR 166

Doxorubicin hydrochloride USP

D005-25MG 25 mg
EUR 301

Doxorubicin Hydrochloride (Autophagy inducer)

SIH-390-10MG 10 mg
EUR 193
Description: The substance Doxorubicin Hydrochloride is a autophagy inducer. It is synthetically produced and has a purity of >98%. The pure substance is red solid which is soluble in water (50 mM)..

Doxorubicin Hydrochloride (Autophagy inducer)

SIH-390-50MG 50 mg
EUR 529
Description: The substance Doxorubicin Hydrochloride is a autophagy inducer. It is synthetically produced and has a purity of >98%. The pure substance is red solid which is soluble in water (50 mM)..

Erlotinib, Hydrochloride Salt

1588-100
EUR 169

Erlotinib, Hydrochloride Salt

1588-1000
EUR 398

Doxorubicin

D063-100MG 100 mg
EUR 1051

Doxorubicin

D063-25MG 25 mg
EUR 322

Doxorubicin

HY-15142A 100mg
EUR 215

Doxorubicin

ADC-P-013 unit Ask for price

Doxorubicin

abx188695-1g 1 g
EUR 467

Doxorubicin

A3966-10 10 mg
EUR 108
Description: Doxorubicin is a semi-synthesized anticancer agent derived from bacterial culture. [1] It is an anthracycline antibiotic. It is been widely used in blood cancers, solid tumors and sarcomas.

Doxorubicin

A3966-100 100 mg
EUR 235
Description: Doxorubicin is a semi-synthesized anticancer agent derived from bacterial culture. [1] It is an anthracycline antibiotic. It is been widely used in blood cancers, solid tumors and sarcomas.

Doxorubicin

A3966-25 25 mg
EUR 131
Description: Doxorubicin is a semi-synthesized anticancer agent derived from bacterial culture. [1] It is an anthracycline antibiotic. It is been widely used in blood cancers, solid tumors and sarcomas.

Doxorubicin

A3966-5.1 10 mM (in 1mL DMSO)
EUR 131
Description: Doxorubicin is a semi-synthesized anticancer agent derived from bacterial culture. [1] It is an anthracycline antibiotic. It is been widely used in blood cancers, solid tumors and sarcomas.

Doxorubicin

A3966-S Evaluation Sample
EUR 81
Description: Doxorubicin is a semi-synthesized anticancer agent derived from bacterial culture. [1] It is an anthracycline antibiotic. It is been widely used in blood cancers, solid tumors and sarcomas.

Erlotinib, Hydrochloride Salt, >99%

BC026-101 1g
EUR 273

Erlotinib, Hydrochloride Salt, >99%

BC026-102 2g
EUR 388

Erlotinib, Hydrochloride Salt, >99%

BC026-105 5g
EUR 570

Adriamycin (Doxorubicin)

E1KS1208 10mg
EUR 409

Doxorubicin HCl

20-abx184016
  • EUR 746.00
  • EUR 1483.00
  • 1 g
  • 5 g

Doxorubicin 10mM

TG4120 0.25ml
EUR 156

17-DMAG, Hydrochloride Salt, >98%

BC024-001 1mg
EUR 178

17-DMAG, Hydrochloride Salt, >98%

BC024-005 5mg
EUR 286

17-DMAG, Hydrochloride Salt, >98%

BC024-010 10mg
EUR 408

17-DMAG, Hydrochloride Salt, >98%

BC024-025 25mg Ask for price

17-DMAG, Hydrochloride Salt, >99%

BC024-100 100mg Ask for price

17-DMAG, Hydrochloride Salt, >99%

BC024-101 1g Ask for price

17-DMAG, Hydrochloride Salt, >99%

BC024-250 250mg Ask for price

OSU-03012, Hydrochloride Salt, >98%

BC061-005 5mg
EUR 313

OSU-03012, Hydrochloride Salt, >98%

BC061-025 25mg
EUR 529

Doxorubicin HCl, 100mg

R2531-100mg
EUR 1300

Doxorubicin HCl, 10mg

R2531-10mg
EUR 197

Doxorubicin (Adriamycin) HCl

A1832-10 10 mg
EUR 125
Description: Doxorubicin is a semi-synthesized anticancer agent derived from bacterial culture. [1] It is an anthracycline antibiotic. It is been widely used in blood cancers, solid tumors and sarcomas.

Doxorubicin (Adriamycin) HCl

A1832-100 100 mg
EUR 467
Description: Doxorubicin is a semi-synthesized anticancer agent derived from bacterial culture. [1] It is an anthracycline antibiotic. It is been widely used in blood cancers, solid tumors and sarcomas.

Doxorubicin (Adriamycin) HCl

A1832-25 25 mg
EUR 189
Description: Doxorubicin is a semi-synthesized anticancer agent derived from bacterial culture. [1] It is an anthracycline antibiotic. It is been widely used in blood cancers, solid tumors and sarcomas.

Doxorubicin (Adriamycin) HCl

A1832-5.1 10 mM (in 1mL DMSO)
EUR 113
Description: Doxorubicin is a semi-synthesized anticancer agent derived from bacterial culture. [1] It is an anthracycline antibiotic. It is been widely used in blood cancers, solid tumors and sarcomas.

Anti-EGFR-doxorubicin ADC

ADC-W-600 1mg Ask for price
Description: This ADC product is comprised of an anti-EGFR monoclonal antibody conjugated via a linker to a doxorubicin

Anti-CD22-DIBO-doxorubicin ADC

ADC-W-339 1mg Ask for price
Description: This ADC product is comprised of an anti-CD22 monoclonal antibody conjugated via a DIBO linker to a doxorubicin

Anti-TNFRSF8 (cAC10)-DIBO-doxorubicin ADC

ADC-W-406 1mg Ask for price
Description: This ADC product is comprised of an anti-TNFRSF8 monoclonal antibody (cAC10) conjugated via a DIBO linker to a doxorubicin

Anti-ERBB2 (Trastuzumab)-NGM-doxorubicin ADC

ADC-W-412 1mg Ask for price
Description: This ADC product is comprised of an anti-ERBB2 monoclonal antibody conjugated via a NGM linker to adoxorubicin

Anti-EGFR (cetuximab)-SMCC-Doxorubicin ADC

ADC-W-504 1mg Ask for price
Description: This ADC product is comprised of an anti-EGFR monoclonal antibody (cetuximab) conjugated via a SMCC linker to Doxorubicin

Anti-EpCAM (MOC31)-hydrazone-Doxorubicin ADC

ADC-W-581 1mg Ask for price
Description: This ADC product is comprised of an anti-EPCAM monoclonal antibody (MOC31) conjugated via a hydrazone linker to Doxorubicin

Anti-FUT3 (clone cBR96)-hydrazone-doxorubicin ADC

ADC-W-423 1mg Ask for price
Description: This ADC product is comprised of an anti-FUT3 monoclonal antibody (clone cBR96) conjugated via a hydrazone linker to adoxorubicin

Anti-CD70 (clone h1F6)-β-glucuronide-doxorubicin ADC

ADC-W-376 1mg Ask for price
Description: This ADC product is comprised of an anti-CD70 monoclonal antibody (clone h1F6) conjugated via a β-glucuronide linker to a doxorubicin

Bile salt

BB0225 25g
EUR 79.58

Anti-TNFRSF8 (cCA10)-β-glucuronide-doxorubicin propyloxazoline (DPO) ADC

ADC-W-353 1mg Ask for price
Description: This ADC product is comprised of an anti-TNFRSF8 monoclonal antibody (cCA10) conjugated via a β-glucuronide linker to a doxorubicin propyloxazoline (DPO)

Human HeLa (Cervix Adenocarcinoma) Cell Nuclear Extract - Doxorubicin Stimulated

HCL-2004 100ug
EUR 225

Human HeLa (Cervix Adenocarcinoma) Whole Cell Lysate - Doxorubicin Stimulated

HCL-2010 100ug
EUR 213

THZ1 hydrochloride

9544-25
EUR 1023

THZ1 hydrochloride

9544-5
EUR 305

Bestatin hydrochloride

9630-25
EUR 457

Bestatin hydrochloride

9630-5
EUR 153

Ambroxol hydrochloride

9688-100
EUR 142

Ambroxol hydrochloride

9688-500
EUR 262

Tetracycline, Hydrochloride

CH054 25 g
EUR 119

Tetracycline, Hydrochloride

CH055 100 g
EUR 170

Palmatine hydrochloride

TB0031 10X20mg
EUR 274

Triacetonamine hydrochloride

TB01047 unit Ask for price

Berberine hydrochloride

TB0119-1000 8XX20mg
EUR 274

Betaine hydrochloride

TB0136 8XX20mg
EUR 274

Sinomenine Hydrochloride

TB0150 6X20mg
EUR 257

Ligustrazine Hydrochloride

TB0189 10X20mg
EUR 274

Jatrorrhizine Hydrochloride

TB0285 3X20mg
EUR 291

Leonurine Hydrochloride

TB0408-0020 20mg
EUR 228

Leonurine hydrochloride

TB0539 3X20mg
EUR 291

Berbamine hydrochloride

TB0619 8XX20mg
EUR 274

Harmine hydrochloride

TB0656 5X20mg
EUR 274

Trigonelline hydrochloride

TB0720-0500 8XX20mg
EUR 274

Tomatidine hydrochloride

TB0825-0025 20mg
EUR 291

Norglaucine hydrochloride

TBP03165 5mg
EUR 1144

Dehydroevodiamine hydrochloride

TBP03315 unit Ask for price
  • haemulonii species complicated elevated from 0.9% (18 isolates amongst 1931) within the first interval (December 2008 to June 2013) to 1.7% (31 isolates amongst 1868) within the second interval (July 2014 to December 2019) of research (p = 0.047).
  • All isolates examined exhibited excessive minimal inhibition concentrations for amphotericin B and fluconazole, however they remained inclined to 5-fluorocytosine and anidulafungin. We had been capable of display the elevated isolation of the multiresistant Candida haemulonii species complicated in our tradition assortment, the place most isolates had been cultured from sufferers with deep-seated infections.

Key phrases: Candida haemulonii species complicated; antifungal resistance; candidemia; cryptic Candida species; nosocomial fungal infections.

Erlotinib, Hydrochloride Salt

We report on a thermally steady monolithic Doppler uneven spatial heterodyne (DASH) interferometer with field-widening prisms for thermospheric wind measurements by observing the Doppler shift of the airglow emission.

gel casting base for evs3100

EVS3100-BASE ea
EUR 301

gel casting base for evs3200

EVS3200-BASE ea
EUR 301

gel casting base for evs3300

EVS3300-BASE ea
EUR 301

THZ1 (Free base)

9664-25
EUR 1023

THZ1 (Free base)

9664-5
EUR 294

PLX5622 (free base)

B2965-25 25 mg
EUR 753

PLX5622 (free base)

B2965-5 5 mg
EUR 227

Vatalanib, Free Base

2026-25
EUR 305

Vatalanib, Free Base

2026-5
EUR 126

Erlotinib, Free Base

2048-100
EUR 158

Erlotinib, Free Base

2048-1000
EUR 387

Linsitinib, Free base

2294-25
EUR 566

Linsitinib, Free base

2294-5
EUR 185

Tipifarnib, Free base

2296-1
EUR 142

Tipifarnib, Free base

2296-5
EUR 414

Sunitinib, Free base

2097-100
EUR 191

Sunitinib, Free base

2097-1000
EUR 501

Sunitinib, Free base

2097-25
EUR 115

Lapatinib, Free base

2138-100
EUR 387

Lapatinib, Free base

2138-25
EUR 191

Ruxolitinib, Free base

2139-100 Ask for price

Ruxolitinib, Free base

2139-25
EUR 533

Ruxolitinib, Free base

2139-5
EUR 207

Imatinib, Free base

2141-100
EUR 147

Imatinib, Free base

2141-1000
EUR 419

Apatinib (Free base)

B1613-25
EUR 414

Apatinib (Free base)

B1613-5
EUR 142

Carubicin (Free base)

B1853-1
EUR 153

Carubicin (Free base)

B1853-5
EUR 457

FIPI (free base)

B2372-25
EUR 631

FIPI (free base)

B2372-5
EUR 196

Terbinafine (Free base)

B2423-250
EUR 207

Terbinafine (Free base)

B2423-50
EUR 120

MCC950 (Free base)

B1031-1
EUR 153

MCC950 (Free base)

B1031-5
EUR 457

YM158 (free base)

HY-U00355 1mg
EUR 2309

RPR107393 free base

HY-100299 1mg
EUR 481

FR167344 free base

HY-100301 1mg
EUR 2637

FR183998 free base

HY-100302 1mg
EUR 1127

FR194738 free base

HY-100303 1mg
EUR 1990

Vatalanib (free base)

HY-10203 5mg
EUR 119

Masupirdine (free base)

HY-109118 1mg
EUR 223

R406 (free base)

HY-11108 10mM/1mL
EUR 231

ITI214 (free base)

HY-12501 100mg
EUR 2943

AS2863619 (free base)

HY-126675 5mg
EUR 1175

AZD3839 (free base)

HY-13438 50mg
EUR 1014

Ripasudil free base

HY-15685A 10mg
EUR 408

AZD4547, Free Base

ADC-P-063 unit Ask for price

AZD8055, Free Base

ADC-P-064 unit Ask for price

Cyclopamine, Free Base

ADC-P-079 unit Ask for price

Ixabepilone, Free Base

ADC-P-104 unit Ask for price

R406(free base)

E1KS1533 2mg
EUR 521

TMB free base

TB0954 1g
EUR 70.88

LY2835219 free base

A3575-100 100 mg
EUR 572
Description: LY2835219 is an orally available cyclin-dependent kinase (CDK) inhibitor that targets the CDK4 (cyclin D1) and CDK6 (cyclin D3) cell cycle pathway, with potential antineoplastic activity.

LY2835219 free base

A3575-25 25 mg
EUR 258
Description: LY2835219 is an orally available cyclin-dependent kinase (CDK) inhibitor that targets the CDK4 (cyclin D1) and CDK6 (cyclin D3) cell cycle pathway, with potential antineoplastic activity.

LY2835219 free base

A3575-5 5 mg
EUR 142
Description: LY2835219 is an orally available cyclin-dependent kinase (CDK) inhibitor that targets the CDK4 (cyclin D1) and CDK6 (cyclin D3) cell cycle pathway, with potential antineoplastic activity.

R406 (free base)

A5880-100 100 mg
EUR 1210
Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins.

R406 (free base)

A5880-25 25 mg
EUR 514
Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins.

R406 (free base)

A5880-5 5 mg
EUR 166
Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins.

R406 (free base)

A5880-5.1 10 mM (in 1mL DMSO)
EUR 264
Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins.

R406 (free base)

A5880-S Evaluation Sample
EUR 81
Description: R406 is a potent SYK inhibitorSpleen tyrosine kinase (SYK) is a non-receptor tyrosine kinase mainly expressed in hematopoietic cells. It transmits signals from a variety of cell surface receptors including CD74, Fc receptor and integrins.

Rucaparib (free base)

A8893-10 10 mg
EUR 200
Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway.

Rucaparib (free base)

A8893-200 200 mg
EUR 1036
Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway.

Rucaparib (free base)

A8893-5 5 mg
EUR 137
Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway.

Rucaparib (free base)

A8893-5.1 10 mM (in 1mL DMSO)
EUR 142
Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway.

Rucaparib (free base)

A8893-50 50 mg
EUR 456
Description: Rucaparib, also named as AG-014699 or PF-01367338, is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway.

Xylazine (free base)

Q-1445.0025 25.0g
EUR 321
Description: Sum Formula: C12H16N2S; CAS# [7361-61-7]

RGB-286638,  free base

2886-25
EUR 756

RGB-286638,  free base

2886-5
EUR 229

StemRegenin 1, Free base

2642-1
EUR 131

StemRegenin 1, Free base

2642-5
EUR 332

GSK-J4 (Free base)

2762-1
EUR 120

GSK-J4 (Free base)

2762-5
EUR 262

BMS-345541 (Free base)

B1907-1
EUR 142

BMS-345541 (Free base)

B1907-5
EUR 414

UNC-926, free base

B2158-25
EUR 631

UNC-926, free base

B2158-5
EUR 196

Analytical deduction and numerical simulation are utilized to find out the central optical path distinction, the thermal compensation situation and the field-widening design. A monolithic interferometer with optimized configuration was constructed and examined within the laboratory.

Laboratory checks present that the very best visibility of 0.94 was realized with the 9 ° field-of-view illumination, whereas the thermal responses of the spatial frequency and the optical section offset are 0.0154 cm-1/°C and 0.469 rad/°C, respectively.