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Penicillin G is an effective penicillin antibiotic Penicillin G can be used for bacterial infection
- Penicillin G
- PENICILLIN G K-SALT
- PENICILLIN G POTASSIUM
- PENICILLIN G POTASSIUM SALT
- (5r,6r)-benzylpenicillin
- (phenylmethyl)-penicilli
- (phenylmethyl)penicillin
- (phenylmethyl)-penicillinicaci
- (phenylmethyl)penicillinicacid
- PENICILLIN
- abbocillin
- benzyl penicillin
- cilloral
- cilopen
- cosmopen
- dropcillin
- galofak
- gelacillin
- pencilling
- pradupen
- Ursopen
- (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- C16H18N2O4S.K
- KBio3_001683
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]- (2S,5R,6R)-
- Free benzylpenicillin
- NCGC00159348-02
- BRD-K55191674-236-03-7
- 61-33-6
- (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid
- CHEBI:18208
- Benzylpenicillin [INN:BAN]
- Bencilpenicilina
- UNII-Q42T66VG0C
- 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-, (2S-(2alpha,5alpha,6beta))-
- NSC-193396
- DB01053
- PHENOXYMETHYLPENICILLIN POTASSIUM IMPURITY A [EP IMPURITY]
- 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6- (2-phenylacetamido)-
- BRD-K55191674-237-12-6
- BSPBio_001096
- KBio2_001413
- (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid
- Phenylacetamidopenicillanic acid
- Pfizerpen
- (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- SBI-0051476.P003
- Benzylpenicillinum (Latin)
- Penicillin-G potassium
- HY-N7139
- (2S,5R,6R)-3,3-dimethyl-7-oxo-6-
- GTPL4796
- DRG-0128
- Benzylpenicillin 1000 microg/mL in Acetonitrile:Water
- Benzylpenicillinum
- 4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-, (2S,5R,6R)-
- 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)- (2S-(2alpha,5alpha,6beta))-
- Pharmacillin
- (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid
- PHENOXYMETHYLPENICILLIN IMPURITY A [EP IMPURITY]
- Benzylpenicillinic acid
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- [2S-(2alpha,5alpha,6beta)]-
- Prestwick3_001078
- KBio2_006549
- EINECS 204-038-0
- Benzylpenicillin [BAN:INN]
- Benzylpenicillinum [Latin]
- Prestwick2_001078
- Penicillin G Potassium in Plastic Container
- (2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]
- EINECS 200-506-3
- SMR000538912
- LS-149836
- CHEMBL29
- IDI1_000316
- BENZYLPENICILLIN (MART.)
- C16H18N2O4S
- NSC193396
- KBio1_000316
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-
- Penicillin,(S)
- GLXC-25718
- benzyl benicillin
- C05551
- Free penicillin G
- 3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid anion (Penicillin G)
- PENICILLIN G [HSDB]
- PENTIDS '250'
- 4-27-00-05861 (Beilstein Handbook Reference)
- BENZYLPENICILLIN [INN]
- JGSARLDLIJGVTE-MBNYWOFBSA-N
- SCHEMBL3783
- bensylpenicillin
- Free penicillin II
- Benzylpenicilline potassique [DCF]
- Q258450
- PENTIDS '400'
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- (2S,5R,6R)-
- MLS001032123
- Benzylpenicillinic acid potassium salt
- BRD-K55191674-237-02-7
- KBioSS_001413
- Penicillinic acid, benzyl-
- CS-0013727
- Benzylpenicillin
- Cillora
- PENICILLIN G [VANDF]
- BDBM50022787
- AKOS005203091
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- [2S-(2.alpha.,5.alpha.,6.beta.)]-, monopotassium salt
- Benzylpenicilline [French]
- MLS000766897
- Q42T66VG0C
- PENICILLIN-2
- NCGC00159348-03
- PHENOXYMETHYLPENICILLIN (BENZATHINE) TETRAHYDRATE IMPURITY A [EP IMPURITY]
- DTXCID3026934
- Cosmopen potassium salt
- Potassium 3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azbicyclo[3.2.0]heptane-2-carboxylate
- PenicillinG
- Phenylacetyl-6-aminopenicillanic acid
- Spectrum4_000471
- Pencillin G
- Penicillinic acid, (phenylmethyl)-
- BENZYLPENICILLIN [MART.]
- PENICILLIN-G
- DTXSID5046934
- NINDS_000316
- 6-(2-phenylacetamido)penicillansyre
- D02336
- Prestwick0_001078
- Benzylpenicillin G
- KBioGR_000942
- Bencilpenicilina [Spanish]
- PENICILLIN G [MI]
- 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-
- 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)- (2S-(2alpha,5alpha,6beta))-, monopotassium salt
- Spectrum_000933
- EN300-19631164
- 3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid
- Benzylpenicillin (INN)
- DivK1c_000316
- Epitope ID:114070
- HMS2875L09
- 3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid(penicillin G)
- potassium [2S-(2alpha,5alpha,6beta)]-3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
- Prestwick1_001078
- Spectrum2_000518
- SPBio_002998
- NSC 193396
- W-109262
- Spectrum3_000542
- HSDB 3166
- Spectrum5_001108
- KBio2_003981
- SPBio_000475
- Compocillin G
- Benzyl-6-aminopenicillinic acid
- BRN 0044740
- A833169
- Bicillin (*Benzathine Salt, Tetrahydrate*)
- MLS001173382
- Benzopenicillin
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- [2S-(2.alpha.,5.alpha.,6.beta.)]-
- (Phenylmethyl)penicillinic acid
- BENZYLPENICILLIN [WHO-DD]
- D00QAR
- BSPBio_002183
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- (2S,5R,6R)-, monopotassium salt
- (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid
- J01CE01
- NSC 131815
- PENTIDS '800'
- Cilloral potassium salt
- Liquacillin
- 2,2-dimethyl-6beta-(phenylacetamido)penam-3alpha-carboxylic acid
- (+)-3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid(penicillin G)
- BPBio1_001206
- (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid
- C16-H18-N2-O4-S.K
- 6-(2-Phenylacetamido)penicillanic acid
- Benzylpenicilline
- (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- PHENOXYMETHYLPENICILLIN IMPURITY A (EP IMPURITY)
- Penicillin, (phenylmethyl)-
- Specilline G
- (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- Benzylpenicillin, Antibiotic for Culture Media Use Only
- NS00068016
- (2S,6R)-3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid
- NSC131815
- NCI60_000703
- FT-0631271
- SB74416
- FT-0770573
- WLN: T45 ANV ESTJ CMV1R& F F GVQ
- CHEMBL300052
- (5S)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- NS00001514
- 3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- SCHEMBL2109546
- 3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- [2S-(2.alpha.,5.alpha.,6.beta.)]-
- DTXSID30859048
- Oprea1_861345
- Cillin
- NSC11964
- 7005-30-3
- AKOS030242685
- 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
- 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,3-dimethyl-7-oxo-6-(2-phenylacetamido)-
- DTXSID20274362
- NSC-11964
- Oprea1_713794
- Galofak
- BRD-K55191674-236-07-8
- Gelacillin
- Cilloral
- (5R,6R)-Benzylpenicillin
- Cilopen
- Benzyl penicillin
- 4,1-Thiaazabicyclo[3.2.0]heptane-2-carboxylic acid, 6-benzylcarbonylamino-3,3-dimethyl-7-oxo-
- BRD-K55191674-237-18-3
- BRD-K55191674-236-06-0
- Pradupen
- (2S,5R,6R)-3,3-DIMETHYL-7-OXO-6-[(PHENYLACETYL)AMINO]-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID
- Dropcillin
- (Phenylmethyl)penicillin
- Cosmopen
- penicillin g
- Penicillin
- MDL：MFCD00069665
- InChIKey：JGSARLDLIJGVTE-MBNYWOFBSA-N
- Inchi：1S/C16H18N2O4S/c1-16(2)12(15(21)22)18-13(20)11(14(18)23-16)17-10(19)8-9-6-4-3-5-7-9/h3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22)/t11-,12+,14-/m1/s1
- SMILES：CC1([C@@H](N2C([C@@H](NC(CC3=CC=CC=C3)=O)[C@H]2S1)=O)C(O)=O)C
Computed Properties
- Exact Mass: 334.09900
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 6
- Rotatable Bond Count: 5
- Monoisotopic Mass: 334.098728
- Heavy Atom Count: 23
- Complexity: 530
- Isotope Atom Count: 0
- Defined Atom Stereocenter Count: 3
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Covalently-Bonded Unit Count: 1
- XLogP3: nothing
- Tautomer Count: 4
- Surface Charge: 0
- Topological Polar Surface Area: 112
Experimental Properties
- LogP: 1.18960
- PSA: 112.01000
- Refractive Index: 1.6930 (estimate)
- Boiling Point: 663.3°C at 760 mmHg
- Melting Point: 214-217 °C
- Flash Point: 355°C
- Solubility: H2O: 100 mg/mL
- Specific Rotation: D +282° (ethanol)
- Density: 1.2729 (rough estimate)
- RTECS：XH9700000
- WGK Germany：2
- Safety Instruction：S36/37
- Risk Phrases：R42/43
- Dangerous goods sign： Xn
- Storage Condition：Ventilation and low temperature drying
- Hazard Category Code：42/43
- FLUKA BRAND F CODES：10-23
- HS CODE：32041900
- Customs Data：
China Customs Code:
32041900
- 1. A kinetic analysis of the acidic degradation of penicillin G and confirmation of penicillamine as a degradation product David P. Kessler,Isaac Ghebre-Sellassie,Adelbert M. Knevel,Stanley L. Hem J. Chem. Soc. Perkin Trans. 2 1981 1247
- 2. A rapid, simple, high-performance liquid chromatography method for the clinical measurement of beta-lactam antibiotics in serum and interstitial fluid Alaa Riezk,Richard C. Wilson,Timothy M. Rawson,Vasin Vasikasin,Paul Arkel,Trevor J. Ferris,Lisa D. Haigh,Anthony E. G. Cass,Alison H. Holmes Anal. Methods 2023 15 829
- 3. A rapid, simple, high-performance liquid chromatography method for the clinical measurement of beta-lactam antibiotics in serum and interstitial fluid Alaa Riezk,Richard C. Wilson,Timothy M. Rawson,Vasin Vasikasin,Paul Arkel,Trevor J. Ferris,Lisa D. Haigh,Anthony E. G. Cass,Alison H. Holmes Anal. Methods 2023 15 829
- 4. The Effect of Cooking on Veterinary Drug Residues in Food.Part 8. Benzylpenicillin? Martin D. Rose,John Bygrave,William H. H. Farrington Analyst 1997 122 1095
- 5. A nuclear magnetic resonance study of the degradation of penicillin G in acidic solution Jaques P. Degelaen,Spiros L. Loukas,James Feeney,Gordon C. K. Roberts,Arnold S. V. Burgen J. Chem. Soc. Perkin Trans. 2 1979 86
- 6. Emerging nanotechnologies for targeting antimicrobial resistance Paul J. Weldick,Anheng Wang,Ahmed F. Halbus,Vesselin N. Paunov Nanoscale 2022 14 4018
- 7. Self-immolative linkers in polymeric delivery systems Christopher A. Blencowe,Andrew T. Russell,Francesca Greco,Wayne Hayes,David W. Thornthwaite Polym. Chem. 2011 2 773
- 8. β-Lactam antibiotic targets and resistance mechanisms: from covalent inhibitors to substrates Montserrat Mora-Ochomogo,Christopher T. Lohans RSC Med. Chem. 2021 12 1623
- 9. Derivatives of 6-aminopenicillanic acid. Part X. A non-enzymic conversion of benzylpenicillin into semi-synthetic penicillins G. R. Fosker,K. D. Hardy,J. H. C. Nayler,P. Seggery,E. R. Stove J. Chem. Soc. C 1971 1917
- 10. Prescribed drugs containing nitrogen heterocycles: an overview Majid M. Heravi,Vahideh Zadsirjan RSC Adv. 2020 10 44247
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(E)-Dimethyl fumarate CAS No.: 624-49-7 -
Methyl sulfoxide CAS No.: 67-68-5 -
Ampicillin sodium CAS No.: 69-52-3 -
Ampicillin Trihydrate CAS No.: 69-53-4 -
penicillin CAS No.: 69-57-8 -
Benzylpenicillin potassium CAS No.: 113-98-4 -
Ampicillin Trihydrate CAS No.: 7177-48-2 -
Amoxycillin CAS No.: 26787-78-0 -
Amoxicillin Sodium CAS No.: 34642-77-8 -
azlocillin sodium CAS No.: 37091-65-9
| Brand:a2bchem | Supplier:A2B Chem LLC | ||||||
|---|---|---|---|---|---|---|---|
| No. | Purity | Stock | Specification | Price | update time | operate | |
| AX46090-1g | 1 week | 1g | $639.00 | 19 Apr. 2024 | |||
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