Thermo Scientific Chemicals Mitomycin C, enthält 2 mg Mitomycin C und 48 mg NaCl
Mitomycin C (CAS-Nr. 50-07-7) ist ein Methylazirinopyrroloindoledion-Komplex, der aus dem Bakterium Streptomyces caespitosus und anderen Streptomyces-Bakterienarten isoliert wird.Es ist eine vielseitige und potente Verbindung mit antibiotischer Wirkung und kann einen potenziellen therapeutischen Wert bei der Behandlung von Krebs haben.
Thermo Scientific Chemicals Ciprofloxacin, 98 %
CAS: 85721-33-1 Summenformel: C17H18FN3O3 Molekulargewicht (g/mol): 331.34 InChI-Schlüssel: MYSWGUAQZAJSOK-UHFFFAOYSA-N Synonym: ciprofloxacin,ciprofloxacine,ciprobay,ciproxan,ciprofloxacina,cipro,ciprofloxacino,ciprofloxacinum,cipro iv,bacquinor PubChem CID: 2764 ChEBI: CHEBI:100241 IUPAC-Name: 1-cyclopropyl-6-fluor-4-oxo-7-piperazin-1-ylchinolin-3-Carbonsäure SMILES: C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=O)O
Thermo Scientific Chemicals Anhydrotetracyclin Hydrochlorid, 'kann als sekundärer Standard verwendet werden'
CAS: 13803-65-1 Summenformel: C22H23ClN2O6 Molekulargewicht (g/mol): 446.88 MDL-Nummer: MFCD00151453 InChI-Schlüssel: FFZXKJVSZDKEMY-XGRJIHFXNA-N Synonym: anhydrotetracycline hydrochloride,unii-ovg14h105r,anhydrotetracycline hcl,c22h22n2o7.hcl,2-naphthacenecarboxamide, 4-dimethylamino-1,4,4a,5,12,12a-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-, monohydrochloride, 4s-4alpha,4aalpha,12aalpha,4-dimethylamino-1,4,4a,5,12,12a-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-2-naphthacenecarboxamide monohydrochloride, 4s-4alpha,4aalpha,12aalpha,anhydrotetracycline hydrochloride, vetranal tm , analytical standard,anhydrotetracycline hydrochloride, certified reference material, tracecert r,anhydrotetracycline hydrochloride, european pharmacopoeia ep reference standard,anhydrotetracycline hydrochloride, united states pharmacopeia usp reference standard PubChem CID: 54710409 IUPAC-Name: hydrogen (2Z)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-11,12a-dihydroxy-6-methyl-1,2,3,4,4a,5,12,12a-octahydrotetracene-1,3,12-trione chloride SMILES: [H+].[Cl-].CN(C)C1C2CC3=C(C(O)=C4C=CC=CC4=C3C)C(=O)C2(O)C(=O)\C(=C(\N)O)C1=O
Sonderaktionen verfügbar
Benzalkoniumchlorid, Alkyl-Verteilung von C8H17 nach C16H33, Thermo Scientific Chemicals
CAS: 8001-54-5 Summenformel: C9H13ClN Molekulargewicht (g/mol): 170.66 MDL-Nummer: MFCD00145757 Synonym: Alkyl-benzyl-dimethylammonium chloride
Thermo Scientific Chemicals Chloramphenicol, 98 %
CAS: 56-75-7 Summenformel: C11H12Cl2N2O5 Molekulargewicht (g/mol): 323.126 MDL-Nummer: MFCD00078159 InChI-Schlüssel: WIIZWVCIJKGZOK-RKDXNWHRSA-N Synonym: Chloromycetin,D(-)-threo-2, 2-Dichloro-N-[β-hydroxy-α-(hydroxy-methyl)-p-nitrophenylethyl]acetamide PubChem CID: 5959 ChEBI: CHEBI:17698 IUPAC-Name: 2,2-Dichlor-N-[(1R,2R)-1,3-Dihydroxy-1-(4-Nitrophenyl)propan-2-yl]acetamid SMILES: C1=CC(=CC=C1C(C(CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]
Sulfanilamid, 98 %, Thermo Scientific Chemicals
CAS: 63-74-1 Summenformel: C6H8N2O2S Molekulargewicht (g/mol): 172.202 MDL-Nummer: MFCD00007939 InChI-Schlüssel: FDDDEECHVMSUSB-UHFFFAOYSA-N Synonym: Sulfanilamid,Sulfamin,Sulfonamid,P-aminobensulfonamid,Sulfonylamid,P-Aminobenzensulfonamid,Bakteriamid,p-aminobenzenesulfamide,bacteramid,streptasol PubChem CID: 5333 ChEBI: CHEBI:45373 IUPAC-Name: 4-aminobenzolsulfonamid SMILES: C1=CC(=CC=C1N)S(=O)(=O)N
Thermo Scientific Chemicals Vancomycin-Hydrochlorid, molekularbiologische Qualität
CAS: 1404-93-9 Summenformel: C66H76Cl3N9O24 Molekulargewicht (g/mol): 1485.72 MDL-Nummer: MFCD03613611,MFCD03613611 InChI-Schlüssel: LCTORFDMHNKUSG-UHFFFAOYNA-N PubChem CID: 124080918 IUPAC-Name: 48-({3-[(4-amino-5-hydroxy-4,6-dimethyloxan-2-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl}oxy)-22-(carbamoylmethyl)-5,15-dichloro-2,18,35,37-pentahydroxy-19-[4-methyl-2-(methylamino)pentanamido]-20,23,26,42,44-pentaoxo-7,13-dioxa-21,24,27,41,43-pentaazaoctacyclo[26.14.2.2³,⁶.2¹⁴,¹⁷.1⁸,¹².1²⁹,³³.0¹⁰,²⁵.0³⁴,³⁹]pentaconta-3,5,8(48),9,11,14,16,29(45),30,32,34,36,38,46,49-pentadecaen-40-carbonsäure Hydrochlorid SMILES: Cl.CNC(CC(C)C)C(=O)NC1C(O)C2=CC(Cl)=C(OC3=CC4=CC(OC5=C(Cl)C=C(C=C5)C(O)C5NC(=O)C(NC(=O)C4NC(=O)C(CC(N)=O)NC1=O)C1=CC(=C(O)C=C1)C1=C(O)C=C(O)C=C1C(NC5=O)C(O)=O)=C3OC1OC(CO)C(O)C(O)C1OC1CC(C)(N)C(O)C(C)O1)C=C2
Amphotericin B, Streptomyces nodosus, Thermo Scientific Chemicals
CAS: 1397-89-3 Summenformel: C47H73NO17 Molekulargewicht (g/mol): 924.09 MDL-Nummer: MFCD00877763 InChI-Schlüssel: APKFDSVGJQXUKY-ZNVUZQDLSA-N PubChem CID: 134129663 IUPAC-Name: (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19Z,21Z,23Z,25Z,27Z,29Z,31Z,33R,35S,36R,37S)-33-{[(2R,3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy}-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaen-36-Carbonsäure SMILES: C[C@H]1O[C@@H](O[C@@H]2C[C@@H]3O[C@@](O)(C[C@H](O)[C@H]3C(O)=O)C[C@@H](O)C[C@@H](O)[C@H](O)CC[C@@H](O)C[C@@H](O)CC(=O)O[C@@H](C)[C@H](C)[C@H](O)[C@@H](C)\C=C/C=C\C=C/C=C\C=C/C=C\C=C/2)[C@@H](O)[C@@H](N)[C@@H]1O
Thermo Scientific Chemicals Gentamicin Sulfat
CAS: 1405-41-0 Synonym: Garamycin,Gentamicin Sulfate
Thermo Scientific Chemicals Sulfanilamid 98 %
CAS: 63-74-1 Summenformel: C6H8N2O2S Molekulargewicht (g/mol): 172.202 MDL-Nummer: MFCD00007939 InChI-Schlüssel: FDDDEECHVMSUSB-UHFFFAOYSA-N Synonym: 4-Aminobenzenesulfonamide PubChem CID: 5333 ChEBI: CHEBI:45373 IUPAC-Name: 4-Aminobenzensulfonamid SMILES: C1=CC(=CC=C1N)S(=O)(=O)N
Thermo Scientific Chemicals Rifampin, 95 %
CAS: 13292-46-1 Summenformel: C43H58N4O12 Molekulargewicht (g/mol): 822.953 InChI-Schlüssel: FZYOVNIOYYPUPY-HRJPTAQKSA-N PubChem CID: 131839595 SMILES: CC1C=CC=C(C(=O)NC2=C(C3=C(C(=C4C(=C3C(=O)C2=CNN5CCN(CC5)C)C(=O)C(O4)(OC=CC(C(C(C(C(C(C1O)C)O)C)OC(=O)C)C)OC)C)C)O)O)C
Puromycin, 10 mg/ml in destilliertem Wasser, steril filtriert, Thermo Scientific Chemicals
CAS: 58-58-2 Summenformel: C22H31Cl2N7O5 Molekulargewicht (g/mol): 544.43 MDL-Nummer: MFCD00150080 InChI-Schlüssel: MKSVFGKWZLUTTO-MLYJQVMKNA-N PubChem CID: 439530 ChEBI: CHEBI:17939 SMILES: Cl.Cl.COC1=CC=C(C[C@H](N)C(=O)N[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O)N2C=NC3=C(N=CN=C23)N(C)C)C=C1
Streptomycin-Sulfat, Zellkulturreagenz, Thermo Scientific Chemicals
CAS: 3810-74-0 Summenformel: C42H84N14O36S3 Molekulargewicht (g/mol): 1457.376 MDL-Nummer: MFCD00037023 InChI-Schlüssel: QTENRWWVYAAPBI-FFCQDDOVSA-N PubChem CID: 124080941 IUPAC-Name: 2-[(1R,2S,3S,4S,5R,6S)-3-(diaminomethylideneamino)-4-[(2R,3S,4S,5S)-3-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy-4-formyl-4-hydroxy-5-methyloxolan-2-yl]oxy-2,5,6-trihydroxycyclohexyl]guanidin;2-[(1R,2S,3S,4R,5R,6R)-3-( SMILES: CC1C(C(C(O1)OC2C(C(C(C(C2O)O)N=C(N)N)O)N=C(N)N)OC3C(C(C(C(O3)CO)O)O)NC)(C=O)O.CC1C(C(C(O1)OC2C(C(C(C(C2O)O)N=C(N)N)O)N=C(N)N)OC3C(C(C(C(O3)CO)O)O)NC)(C=O)O.OS(=O)(=O)O.OS(=O)(=O)O.OS(=O)(=O)O
Hygromycin B, Thermo Scientific Chemicals
CAS: 31282-04-9 Summenformel: C20H37N3O13 Molekulargewicht (g/mol): 527.524 MDL-Nummer: MFCD06795479 InChI-Schlüssel: GRRNUXAQVGOGFE-BBMONYMYSA-N PubChem CID: 134129613 IUPAC-Name: (3'S,3aS,4S,4'S,5'R,6R,6'R,7R,7aS)-4-[(1R,2S,3R,5S,6S)-3-Amino-2,6-Dihydroxy-5-(methylamino)cyclohexyl]oxy-6'-[(1S)-1-Amino-2-Hydroxyethyl]-6-(hydroxymethyl)spiro[4,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-2,2'-oxan]-3',4',5',7-tetrol SMILES: CNC1CC(C(C(C1O)OC2C3C(C(C(O2)CO)O)OC4(O3)C(C(C(C(O4)C(CO)N)O)O)O)O)N
Thermo Scientific Chemicals 4-Epitetracyclin Hydrochlorid, 'als sek. Standard verwendbar'
CAS: 23313-80-6 Summenformel: C22H24N2O8·HCl Molekulargewicht (g/mol): 480.89 MDL-Nummer: MFCD00865028 InChI-Schlüssel: YCIHPQHVWDULOY-DXDJYCPMSA-N Synonym: 4-epitetracycline hydrochloride,epitetracycline hydrochloride,4-epi-tetracycline hydrochloride,quatrimycin hydrochloride,epitetracycline hcl,unii-i7c3edl2yg,i7c3edl2yg,epitetracycline hydrochloride usp,4r,4as,5as,6s,12as-4-dimethylamino-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide monohydrochloride PubChem CID: 54686189 IUPAC-Name: (4R,4aS,5aS,6S,12aR)-4-(Dimethylamino)-1,6,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracen-2-carboxamid;hydrochlorid SMILES: CC1(C2CC3C(C(=O)C(=C(C3(C(=O)C2=C(C4=C1C=CC=C4O)O)O)O)C(=O)N)N(C)C)O.Cl