Exact Mass: 299.0495214

1-[2-(3-Bromophenoxy)ethyl]-4-piperidinol

1-(8-methyl-6-oxo-[1,3]dioxolo[4,5-g]chromen-7-yl)pyrrole-2,5-dione

C15H9NO6 (299.0429854)

2,6-Diamino-4-(4-nitrophenyl)-4H-thiopyran-3,5-dicarbonitrile

C13H9N5O2S (299.0476934)

N-[3-(1-IMidazolyl)propyl]-4-chlorobenzenesulfonamide

C12H14ClN3O2S (299.0495214)

3-METHYL-2-PERFLOROPROPYL-1H-INDOLE

C12H8F7N (299.0544932)

Diclofenac D4

C14H7Cl2D4NO2 (299.041789312)

gemcitabine hydrochloride

C9H12ClF2N3O4 (299.0484366)

C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite C471 - Enzyme Inhibitor > C2150 - Ribonucleotide Reductase Inhibitor D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents Gemcitabine Hydrochloride (LY 188011 Hydrochloride) is a pyrimidine nucleoside analog antimetabolite and an antineoplastic agent. Gemcitabine Hydrochloride inhibits DNA synthesis and repair, resulting in autophagyand apoptosis[1][2].

4-BROMO-N-(TERT-BUTYL)-2-ETHOXYBENZAMIDE

2,6-diamino-4-(2-nitrophenyl)-4H-thiopyran-3,5-dicarbonitrile

C13H9N5O2S (299.0476934)

N-BOC-2-(4-BROMOPHENYL)ETHYLAMINE

N-Methyl-N-trimethylsilylheptafluorobutyramide

C8H12F7NOSi (299.0576346)

tert-Butyl 3-(bromomethyl)benzylcarbamate

3-chloro-6-piperazin-1-ylsulfonyl-1H-indole

C12H14ClN3O2S (299.0495214)

(R)-tert-butyl 1-(3-bromophenyl)ethylcarbamate

4,6-diamino-1-(4-chlorophenyl)-2-oxo-3H-pyrrolo[2,3-b]pyridine-5-carbonitrile

C14H10ClN5O (299.057384)

4-bromo-N-butyl-2-ethoxybenzamide

(R)-tert-Butyl (1-(4-bromophenyl)ethyl)carbamate

(4-BROMO-BENZYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER

gemcitabine hydrochloride

C9H11F2N3O4.ClH (299.0484366)

Methyl 2-(3-bromophenyl)norleucinate

2,6-diamino-4-(3-nitrophenyl)-4H-thiopyran-3,5-dicarbonitrile

C13H9N5O2S (299.0476934)

tert-Butyl 4-(bromomethyl)benzylcarbamate

TERT-BUTYL (2-BROMO-4,5-DIMETHYLPHENYL)CARBAMATE

[1-(4-BROMO-PHENYL)-ETHYL]-CARBAMIC ACID TERT-BUTYL ESTER

Leptazoline A

Kaempferide(1-)

Conjugate base of kaempferide arising from selective deprotonation of the 3-hydroxy group.

Pratensein(1-)

4,5-Dihydroxy-3-methoxyflavon-7-olate(1-)

A flavonoid oxoanion that is the conjugate base of 4,5,7-trihydroxy-3-methoxyflavone arising from selective deprotonation of the 7-hydroxy group; major species at pH 7.3.

N-acetyl-D-glucosamine 6-phosphate(2-)

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N-acetyl-mannosamine 6-phosphate

N-acetyl-alpha-D-glucosamine 1-phosphate(2-)

N-acetyl-alpha-D-galactosamine 1-phosphate(2-)

N-acetyl-D-galactosamine 6-phosphate(2-)

Peonidin(1-)

An organic anion obtained by selective deprotonation of the 3- and 5-hydroxy groups of peonidin; major species at pH 7.3.

N-acetyl-beta-D-glucosamine 6-phosphate(2-)

an N-acetyl-alpha-D-hexosamine 1-phosphate

Laccaic acid anthrone

N-acetyl-D-mannosamine 1-phosphate

N-acetyl-alpha-D-glucosamine 6-phosphate

2-Deoxy-2,2-difluorocytidine monohydrochloride

C9H12ClF2N3O4 (299.0484366)

D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents

N-acetyl-D-mannosamine 6-phosphate(2-)

C15H13N3S2 (299.05508580000003)

COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

5-(4-chlorophenyl)-3-(4-nitrophenyl)-1H-pyrazole

C15H10ClN3O2 (299.046151)

Tazobactam(1-)

C10H11N4O5S- (299.0450136)

A penicillinate anion that is the conjugate base of tazobactam, obtained by deprotonation of the carboxy group.

5-methyl-4-phenyl-2-[(2E)-2-(thiophen-2-ylmethylidene)hydrazinyl]-1,3-thiazole

4-phenyl-N-[(E)-1-thiophen-2-ylethylideneamino]-1,3-thiazol-2-amine

C15H13N3S2 (299.05508580000003)

KAEMPFEROL 7-METHYL ETHER

N-acetyl-D-hexosamine 1-phosphate(2-)

Diosmetin-7-olate

A flavonoid oxoanion obtained by deprotonation of the 7-hydroxy group of diosmetin; major microspecies at pH 7.3.

3-O-methylkaempferol 7-olate

Luteolin-5-olate 7-methyl ether

Scutellarein-7-olate 4-methyl ether

4,8-Dihydroxy-3-methoxyflavone-7-olate

3,4,7-Trihydroxy-8-methoxyflavone

N-acetyl-D-glucosamine 6-phosphate(2-)

Dianion of N-acetyl-D-glucosamine 6-phosphate arising from deprotonation of both OH groups of the phosphate.

N-acetyl-alpha-D-glucosamine 1-phosphate(2-)

Dianion of N-acetyl-alpha-D-glucosamine 1-phosphate arising from deprotonation of the phosphate OH groups; major species at pH 7.3.

N-acetyl-D-mannosamine 6-phosphate(2-)

An organophosphate oxoanion resulting from the removal of both protons from the phosphate group of N-acetyl-D-mannosamine 6-phosphate.

N-acetyl-alpha-D-galactosamine 1-phosphate(2-)

An organophosphate oxoanion obtained by deprotonation of the phosphate OH groups of N-acetyl-alpha-D-galactosamine 1-phosphate; major species at pH 7.3.

N-acetyl-beta-D-glucosamine 6-phosphate(2-)

Dianion of N-acetyl-beta-D-glucosamine 6-phosphate.

(3s)-3-[(4r,5r)-2-(5-chloro-2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]-3-hydroxypropanoic acid

[(2r,3s,4s)-4-chloro-5-hydroxy-3-(4-hydroxyphenoxy)-3,4-dihydro-2h-pyrrol-2-yl]methyl acetate

C14H9N3O5 (299.05421839999997)

8-amino-9-(c-hydroxycarbonimidoyl)-7-oxophenoxazine-2-carboxylic acid

[4-chloro-5-hydroxy-3-(4-hydroxyphenoxy)-3,4-dihydro-2h-pyrrol-2-yl]methyl acetate