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| Product | Description | |
|---|---|---|
| Penehyclidine Impurity 5 | Penehyclidine Impurity 5. Uses: For analytical and research use. CAS No. 63624-23-7. Molecular formula: C21H25NO2. Mole weight: 323.44. Catalog: APB63624237. |  |
| Penehyclidine Impurity B | Penehyclidine Impurity B. Uses: For analytical and research use. Molecular formula: C14H20O2. Mole weight: 220.31. Catalog: APB09497. | |
| Penehyclidine Impurity C | Penehyclidine Impurity C. Uses: For analytical and research use. Molecular formula: C33H45NO3. Mole weight: 503.73. Catalog: APB09496. | |
| Penethamate | Penethamate. Alternative Names: Penethamate;penethamate hydroiodide;Penethacillin;PENICILLINGDIETHYLAMINOETHYLESTER;(2S,5β)-3,3-Dimethyl-7-oxo-6α-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2β-carboxylic acid 2-(diethylamino)ethyl ester;(6α-[(Phenylacetyl)amino]penicillanic acid 2-(diethylamino)ethyl) ester. CAS No. 3689-73-4. Purity: 96%. Product ID: ACM3689734. Molecular formula: C22H31N3O4S. Mole weight: 433.57. IUPAC Name: 2-(diethylamino)ethyl(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. Canonical SMILES: CCN(CC)CCOC(=O)C1C(SC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)(C)C. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Penetran Cl | Synthetic, an inhibitor of high-affinity choline uptake (HAChU) in synaptosomes. Grade: ≥ 98%.(TLC). Molecular formula: C14H14NOCl.HCl. Mole weight: 284.18. |  |
| Penetratin | The first 16 amino acids of Penetratin are derived from the third helix of the Antennapedia protein homeodomain, known as the protein transduction domain (PTD). Penetratin linked to phosphodiester oligonucleotides can penetrate neuronal cell membranes and down-regulate genes. It contains a nuclear localization sequence that facilitates internalization of cargo into living cells. Uses: Penetratin, also known as antennapedia homeodomain or penetratin-1, is a cell-penetrating peptide derived from the drosophila antennapedia protein. this short peptide sequence, consisting of 16 amino acids (rqikiwfqnrrmkwkk), has attracted great attention in the biotechnology and medical fields due to its outstanding ability to penetrate cell membranes and deliver a variety of cargo molecules into. Synonyms: H-Arg-Gln-Ile-Lys-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Lys-Trp-Lys-Lys-NH2. Grade: >98%. CAS No. 214556-79-3. Molecular formula: C104H169N35O19S. Mole weight: 2245.78. | |
| Penetratin | Penetratin is a cell-penetrating peptides derived from a nonviral protein. Penetratin can powerfully enhance drug absorption. Penetratin can be used for drug delivery research in the treatment of various diseases[1][2]. Uses: Scientific research. Category: Peptides. CAS No. 940866-75-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2529. |  |
| Penetratin-Arg | Penetratin-Arg, a cell-penetrating peptide (CPP) derived from the 3rd helix of Drosophila Antennapedia homeodomain protein, can permeate cell membrane at low micromolar concentration without significantly affecting membrane. It contains a nuclear localization sequence that facilitates internalization of cargo into living cells. Synonyms: PenArg; H-Arg-Gln-Ile-Arg-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Arg-Trp-Arg-Arg-NH2; L-arginyl-L-glutaminyl-L-isoleucyl-L-arginyl-L-isoleucyl-L-tryptophyl-L-phenylalanyl-L-glutaminyl-L-asparagyl-L-arginyl-L-arginyl-L-methionyl-L-arginyl-L-tryptophyl-L-arginyl-L-argininamide. Grade: >98%. Molecular formula: C104H169N43O19S. Mole weight: 2357.80. | |
| Penetratin-eiF4E | Penetratin-eiF4E. Synonyms: (D-Arg)-(D-Gln)-(D-Ile)-(D-Lys)-(D-Ile)-(D-Trp)-(D-Phe)-(D-Gln)-(D-Asn)-(D-Arg)-(D-Arg)-(D-Met)-(D-Lys)-(D-Trp)-(D-Lys)-(D-Lys)-Ile-Gly-Tyr-Gln-Ser-His-Ala-Asp-Thr-Ala-Thr-Lys-Ser-Gly-Ser-Thr-Thr-Lys-Asn-Arg-Phe-Val-Val. Molecular formula: C215H344N66O57S. Mole weight: 4797.78. | |
| Penetratin Trifluoroacetate | Penetratin, a cell-penetrating peptide (CPP), is renowned for its ability to facilitate the intracellular delivery of various bioactive molecules, including proteins, peptides, nucleic acids, and nanoparticles, across the cell membrane. It shows antimicrobial and antifungal activity. Grade: 98%. Molecular formula: C106H170F3N35O21S. Mole weight: 2359.80. | |
| Penflufen | Penflufen is a highly efficient, broad-spectrum succinate dehydrogenase inhibitor (SDHI). Penflufen can be used as a fungicide and has broad bioactivity against many fungal diseases, including potato black scurf, wheat sharp eyespot, rice sheath blight, and root rot in peanut and other similar fungal diseases[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 494793-67-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139161. | |
| Penfluridol | Penfluridol. Group: Biochemicals. Grades: Highly Purified. CAS No. 26864-56-2. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. |  Worldwide |
| Penfluridol | Penfluridol (TLP-607) is a highly potent antipsychotic. Category: Active pharmaceutical ingredients. CAS No. 26864-56-2. Product ID: API26864562. Molecular formula: C28H27ClF5NO. Mole weight: 523.97. |  |
| Penfluridol | Penfluridol (R-16341) is a potent, long-acting, first-generation, oral diphenylbutylpiperidine antipsychotic agent by targeting D2-like dopamine receptor. Penfluridol effectively inhibits TNFα-induced NF-κB activation and alleviates the severity of arthritis and colitis in vivo. Penfluridol is a Ca2+-calmodulin inhibitor. Penfluridol induces apoptosis and autophagy. Penfluridol is used for chronic schizophrenia, acute psychosis, Tourette syndrome and autoimmune diseases. Penfluridol inhibites the growth of E. faecalis planktonic cells with the MIC of 7.81 μg/ml[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: R-16341. CAS No. 26864-56-2. Pack Sizes: 10 mM * 1 mL in DMSO; 25 mg; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-B1077. | |
| Penguin AvBD103a | Penguin AvBD103a is an antimicrobial peptide found in King Penguin stomach, Aptenodytes patagonicus, and has anti-gram-positive bacteria, gram-negative bacteria and fungal activity. Synonyms: Spheniscin 1; Penguin avian β-defensin 103a; Sphe-1; defensin pBD-1 (King penguin); L-Tryptophan, L-seryl-L-phenylalanylglycyl-L-leucyl-L-cysteinyl-L-arginyl-L-leucyl-L-arginyl-L-arginylglycyl-L-phenylalanyl-L-cysteinyl-L-alanyl-L-histidylglycyl-L-arginyl-L-cysteinyl-L-arginyl-L-phenylalanyl-L-prolyl-L-seryl-L-isoleucyl-L-prolyl-L-isoleucylglycyl-L-arginyl-L-cysteinyl-L-seryl-L-arginyl-L-phenylalanyl-L-valyl-L-glutaminyl-L-cysteinyl-L-cysteinyl-L-arginyl-L-arginyl-L-valyl-, cyclic(5→33),(12→27),(17→34)-tris(disulfide). Grade: >85%. CAS No. 641144-91-4. | |
| Penguin AvBD103b | Penguin AvBD103b is an antimicrobial peptide found in King Penguin stomach, Aptenodytes patagonicus, and has antibacterial activity. Synonyms: Spheniscin 2; Penguin avian β-defensin 103b; Sphe-1; defensin pBD-2 (King penguin); L-Tryptophan, L-seryl-L-phenylalanylglycyl-L-leucyl-L-cysteinyl-L-arginyl-L-leucyl-L-arginyl-L-arginylglycyl-L-phenylalanyl-L-cysteinyl-L-alanyl-L-arginylglycyl-L-arginyl-L-cysteinyl-L-arginyl-L-phenylalanyl-L-prolyl-L-seryl-L-isoleucyl-L-prolyl-L-isoleucylglycyl-L-arginyl-L-cysteinyl-L-seryl-L-arginyl-L-phenylalanyl-L-valyl-L-glutaminyl-L-cysteinyl-L-cysteinyl-L-arginyl-L-arginyl-L-valyl-, cyclic(5→33),(12→27),(17→34)-tris(disulfide). Grade: >85%. CAS No. 641144-92-5. | |
| PEN (human) | PEN (human), one of the most abundant hypothalamic neuropeptide and derived from the proprotein ProSAAS, is an endogenous ligand of GPR83[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 597578-70-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2278. | |
| Penicillamine | Penicillamine is used as an antirheumatic and as a chelating agent in Wilson's disease. Synonyms: Dimethyl Cysteine. Grade: >98%. CAS No. 52-67-5. Molecular formula: C5H11NO2S. Mole weight: 149.21. | |
| Penicillamine Impurity 1 | Penicillamine Impurity 1. Uses: For analytical and research use. CAS No. 22801-32-7. Molecular formula: C10H20N2O4S3. Mole weight: 328.46. Catalog: APB22801327. | |
| Penicillic acid | It is produced by the strain of Pen. puberulum. It is an antibiotic with activity against gram-positive bacteria, negative bacteria and mycobacterium. It is also used as a raw material for various semisynthetic penicillins. Penicillic acid, a kind of polyketide mycotoxin, has been found to restrain GDP-mannose dehydrogenase and sorts of other dehydrogenases. It causes DNA to break. Synonyms: 3-Methoxy-5-methyl-4-oxohexa-2,5-dienoic acid; Penicillinsaure; NSC 402844; γ-Keto-β-methoxy-δ-methylene-Δα-hexenoic Acid; HSDB 3523. Grade: 98%. CAS No. 90-65-3. Molecular formula: C8H10O4. Mole weight: 170.16. | |
| Penicillic acid | Penicillic acid is a polyketide mycotoxin produced by several species of Aspergillus and Penicillium. Penicillic acid exhibits cytotoxicity in rat alveolar macrophages (AM) in vitro. Penicillic acid inhibits Fas ligand-induced apoptosis by blocking self-processing of caspase-8[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 90-65-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-N6777. | |
| Penicillide | Penicillide is an acyl-CoA: cholesterol acyltransferase (ACAT) inhibitor produced by Penicillum asperosporum KY1635. The IC50 for inhibiting ACAT was 22.9 μmol/L. Synonyms: Vermixocin A; AS-186a; 11-hydroxy-3-[(1s)-1-hydroxy-3-methylbutyl]-4-methoxy-9-methyl-5h,7h-dibenzo[b,g][1,5]dioxocin-5-one. Grade: ≥95%. CAS No. 55303-92-9. Molecular formula: C21H24O6. Mole weight: 372.41. | |
| Penicillin | It is produced by the strain of Cephalosporium aceemonium, C. salmosynnematum, Emericellopsis salmosynnemata. It has weak anti-gram-positive bacteria (activity against Staphylococcus aureus is only 1% of penicillin G) and anti-gram-negative bacteria activity, and can be broken down by penicillinase and cross-resistant to penicillin G. Synonyms: Penicillin N; Synnematin B; Cephalosporin N; Adicillin; Salmotin; SYNNEMATINB; Adicillinum; Synnematin N; (2S,5R,6R)-6-(5-Amino-5-carboxyvaleramido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptan-2-carbonsaeure; Cephalosphorin R; 6-N-((5-Amino-5-carboxy)pentanoyl)aminopenicillansaeure; (4-Amino-4-carboxybutyl)penicillin; NSC 113137; (D-4-Amino-4-carboxybutyl) penicillinic acid. Grade: 95%. CAS No. 525-94-0. Molecular formula: C14H21N3O6S. Mole weight: 359.40. | |
| penicillin amidase | This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. The systematic name of this enzyme class is penicillin amidohydrolase. Other names in common use include penicillin acylase, benzylpenicillin acylase, novozym 217, semacylase, alpha-acylamino-beta-lactam acylhydrolase, and ampicillin acylase. This enzyme participates in penicillin and cephalosporin biosynthesis. Group: Enzymes. Synonyms: penicillin acylase; benzylpenicillin acylase; novozym 217; semacylase; α-acylamino-β-lactam acylhydrolase; ampicillin acylase. Enzyme Commission Number: EC 3.5.1.11. CAS No. 9014-6-6. Penicillin Amidase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4389; penicillin amidase; EC 3.5.1.11; 9014-06-6; penicillin acylase; benzylpenicillin acylase; novozym 217; semacylase; α-acylamino-β-lactam acylhydrolase; ampicillin acylase. Cat No: EXWM-4389. |  |
| Penicillin amidase, E. coli (Immobilized) | Penicillin amidase, E. coli (Immobilized) (PGA) is an amidohydrolase commonly used in industrial biocatalysis. Penicillin amidase, E. coli (Immobilized) serves as a starting material in the synthesis of semi-synthetic penicillins. Penicillin amidase, E. coli (Immobilized) promotes the production of semi-synthetic β-lactam antibiotics, participates in peptide synthesis, and catalyzes the formation of chiral compounds. Penicillin amidase, E. coli (Immobilized) is regulated by temperature and phenylacetic acid in E. coli. In free E. coli, it participates in the assimilation of aromatic compounds as a carbon source. Penicillin amidase, E. coli (Immobilized) is hypothesized to act as a scavenging enzyme for phenylacetyl-containing compounds in microbial metabolism and is associated with bacterial quorum sensing[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PGA. CAS No. 9014-6-6. Pack Sizes: 100 mg; 250 mg. Product ID: HY-P2834. | |
| Penicillin DF | Penicillin DF is used to characterize phenylacetate-CoA ligase from Penicillium chrysogenum. Group: Biochemicals. Grades: Highly Purified. CAS No. 4493-18-9. Pack Sizes: 10mg, 50mg. Molecular Formula: C14H22N2O4S, Molecular Weight: 314.399999999999. US Biological Life Sciences. | Worldwide |
| Penicillin F Sodium | It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It is an antibiotic. Synonyms: Sodium penicillin F; 2-Pentenylpenicillin sodium; Sodium 2-pentenylpenicillinate; Penicillin F sodium salt; 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((1-oxo-3-hexenyl)amino)-, monosodium salt, (2S-(2alpha,5alpha,6beta))-. CAS No. 525-86-0. Molecular formula: C14H19N2O4SNa. Mole weight: 334.37. | |
| Penicillin g | Penicillin g. Alternative Names: PENICILLIN G K-SALT;PENICILLIN G POTASSIUM;PENICILLIN G POTASSIUM SALT;(5r,6r)-benzylpenicillin;(phenylmethyl)-penicilli;(phenylmethyl)penicillin;(phenylmethyl)-penicillinicaci;(phenylmethyl)penicillinicacid. CAS No. 61-33-6. Purity: 95%+. Product ID: ACM61336. Molecular formula: C16H18N2O4S. Mole weight: 334.39. IUPAC Name: (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid. Canonical SMILES: CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C. ECNumber: 200-506-3. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Penicillin G | Penicillin G is a β-lactam antibiotic produced by penicillin. Synonyms: Benzylpenicillin; Benzylpenicillinic Acid; Free Penicillin II. CAS No. 61-33-6. Molecular formula: C16H18N2O4S. Mole weight: 334.39. | |
| Penicillin g benzathine | Penicillin g benzathine. Alternative Names: Penicillin G Benzathine Tetrahydrate; Penicillin G benzathine tetrahydrate. CAS No. 41372-02-5. Purity: 96%. Product ID: ACM41372025. Molecular formula: C48H64N6O12S2. Mole weight: 981.18. IUPAC Name: N,N-dibenzylethane-1,2-diamine; (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; tetra. Canonical SMILES: CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C.CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C.C1=CC=C(C=C1)CNCCNCC2=CC=CC=C2.O.O.O.O. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Penicillin G Benzathine | Penicillin G benzathine is the benzathine salt form of natural penicillin G, formulated as a sterile aqueous suspension for deep intramuscular injection only. Due to its extremely low solubility and slow absorption, it is classified as a prescription antibiotic against intravenous administration. Applications: Penicillin g benzathine is indicated for treatment of group a streptococcal upper respiratory infections and for syphilis of all stages including primary, secondary, and latent disease. it serves as the gold standard for rheumatic fever prophylaxis with monthly intramuscular injections and is also used for yaws, bejel, and pinta. Category: Antibacterial apis. Synonyms: Benzathine Penicillin; Benzathine Benzylpenicillin. CAS No. 41372-02-5. Product ID: API0232893. Molecular formula: C48H64N6O12S2. Mole weight: 981.2. EINECS: 804-898-2. InChIKey: WIDKTXGNSOORHA-CJHXQPGBSA-N. Appearance: White crystalline powder. | |
| Penicillin G benzathine anhydrous | Penicillin G benzathine anhydrous. Group: Biochemicals. Alternative Names: Benzathine benzylpenicillin; Benzylpenicillin benzathine. Grades: Highly Purified. CAS No. 1538-09-6. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C16H20N2·2 (C16H18N2O4S). US Biological Life Sciences. | Worldwide |
| Penicillin G-[d7] N-ethylpiperidinium salt | Penicillin G-[d7] N-ethylpiperidinium salt is the labelled salt of Penicillin G, which is an impurity of penicilline. Synonyms: (2S-(2α,5α,6β))-3,3-Dimethyl-7-oxo-6-phenylacetyl-D7-amino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate 1-ethyl-piperidinium; Benzylpenicilline-D7 N-ethylpiperidinium salt; Penicillin G-D7 N-ethylpiperidinium salt. Grade: 95% by HPLC; 98% atom D. CAS No. 1217445-37-8. Molecular formula: C23H26D7N3O4S. Mole weight: 454.63. | |
| Penicillin G-d7 potassium salt | Penicillin G-d7 (potassium) is the deuterium labeled Penicillin G potassium salt[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Benzylpenicillin-d7 potassium salt. CAS No. 352323-25-2. Pack Sizes: 2.5 mg. Product ID: HY-N7139S1. | |
| Penicillin G potassium | Penicillin G potassium is a fast-acting penicillin family antibiotic. Penicillin G potassium can be used for the research of bacterial infections that affect the blood, heart, lungs, joints, and genital areas[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Benzylpenicillin potassium. CAS No. 113-98-4. Pack Sizes: 5 g; 10 g; 25 g; 50 g; 100 g. Product ID: HY-17591. | |
| Penicillin G Potassium | Penicillin G potassium is the potassium salt of natural penicillin G (benzylpenicillin), formulated as a white crystalline powder for parenteral administration. It is supplied as a sterile powder for reconstitution and is intended for intramuscular or intravenous use due to its poor oral absorption and acid lability. Each million units contains approximately 1.7 mEq of potassium, requiring consideration in patients with electrolyte imbalances or renal impairment. Applications: Penicillin g potassium is indicated for serious infections caused by susceptible organisms including streptococci, pneumococci, meningococci, and treponema pallidum. specific indications include streptococcal endocarditis, pneumococcal pneumonia, meningococcal meningitis, anthrax, diphtheria, tetanus, gas gangrene, and neurosyphilis. dosing ranges from 2 to 30 million units daily divided every 4 to 6 hours depending on infection severity, with dosage adjustment required in renal impairment. Category: Antibacterial apis. Synonyms: Pfizerpen, Benzylpenicillin potassium, Potassium benzylpenicillin, Penicillin G potassium salt. CAS No. 113-98-4. Product ID: API0232172. Molecular formula: C16H17KN2O4S. Mole weight: 372.48. EINECS: 204-038-0. InChIKey: IYNDLOXRXUOGIU-LQDWTQKMSA-M. Appearance: Colorless or white crystal, or white crystalline powder. | |
| Penicillin G Potassium Salt | Penicillin G is a narrow spectrum antibiotic derived from Streptococcus pneumoniae. It is the drug of choice for groups A, B, C and G streptococci, nonenterococcal group D streptococci, viridians group streptococci, and non-penicillinase producing staphylococcus. The potassium salt has been used to study murosomes of staphylococci and the penicillin-induced lysis of Streptococcus mutans. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Potassium Salt; Penicillin G Potassium Salt; Benzylpenicillin Potassium; Cosmopen; Cristapen; Crytapen; Eskacillin; Falapen; Forpen; Hipercilina; Hyasorb; Hylenta; M-Cillin; Monopen; NSC 131815; Notaral; Pentid; Pentids; Potassium 6- (Phenylacetamido) penicillanate; Potassium Benzylpenicillin; Potassium Benzylpenicillinate; Potassium Penicillin G; Scotcil; Tabilin. Grades: Cell Culture Grade. CAS No. 113-98-4. Pack Sizes: 100g, 500g, 1Kg. US Biological Life Sciences. | Worldwide |
| Penicillin G potassium salt (Benzylpenicillin potassium salt) | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O4S. CAS No. 113-98-4. Prepack ID 23531529-25g. Molecular Weight 372.48. See USA prepack pricing. |  |
| Penicillin G Sodium | Penicillin G sodium is a natural, parenteral beta-lactam antibiotic derived from Penicillium chrysogenum and represents the original member of the penicillin family. It is available as a crystalline powder for reconstitution and intravenous or intramuscular administration. The drug is acid-labile and therefore ineffective orally, necessitating injectable delivery for systemic effect. Applications: This antibiotic remains the drug of choice for infections caused by non-resistant streptococci, treponema pallidum (syphilis), clostridium perfringens, and neisseria meningitidis. it is also used for pneumococcal pneumonia and endocarditis due to penicillin-susceptible strains. high doses are required for central nervous system infections due to limited penetration, and resistance mediated by beta-lactamase is increasingly encountered. Category: Active pharmaceutical ingredients. Synonyms: Crystapen; Benzylpenicillin sodium; BENZYLPENICILLIN SODIUM SALT; American penicillin; Sodium penicillin G. CAS No. 69-57-8. Product ID: API0231579. Molecular formula: C16H17N2NaO4S. Mole weight: 356.4. EINECS: 200-710-2. InChIKey: FCPVYOBCFFNJFS-LQDWTQKMSA-M. Appearance: White to slightly yellow crystalline powder. | |
| Penicillin G sodium salt | Penicillin G sodium salt is a typical β-lactam antibiotic. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Benzylpenicillin sodium salt. CAS No. 69-57-8. Pack Sizes: 100 mg; 250 mg; 500 mg. Product ID: HY-B1463. | |
| Penicillin G sodium salt | It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It has strong activity of anti-gram-positive bacteria and spirochetes, and has weak anti-gram-negative bacteria activity. It is widely used in clinical practice. Uses: Anti-bacterial agents. Synonyms: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt; 3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium Salt; American Penicillin; Benzylpenicillin Sodium; Benzylpenicillin Sodium Salt; Benzylpenicillinic Acid Sodium Salt; Crystapen; Ethacillin; Monocillin; Monosodium Benzylpenicillin; Mycofarm; Nalpen G; Nobak; Novocillin; Pen-A-Brasive; Penicillin G Sodium; Penilaryn; Sodium 6-(Phenylacetamido)penicillanate; Sodium Benzylpenicillin; Sodium Benzylpenicillin G; Sodium Penicillin; Sodium Penicillin G; NSC 69877; NSC-69877; NSC69877; 7-NO2-ICA. Grade: 98%. CAS No. 69-57-8. Molecular formula: C16H17N2NaO4S. Mole weight: 356.37. | |
| Penicillin G sodium salt (Benzylpenicillin sodium salt) | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N2NaSO4. CAS No. 69-57-8. Prepack ID 47080913-25g. Molecular Weight 356.37. See USA prepack pricing. | |
| Penicillin G sodium salt (Benzylpenicillin sodium salt) | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N2NaSO4. CAS No. 69-57-8. Prepack ID 47080913-5g. Molecular Weight 356.37. See USA prepack pricing. | |
| Penicillin G, Sodium Salt USP | Penicillin G is a broad based antibiotic used in mammalian cell culture. Penicillin G blocks the formation of bacterial cell walls, rendering bacteria unable to multiply and spread. The spectrum of activity of Penicillin G includes many aerobic and anaerobic gram-positive organisms. Aerobes susceptible to Penicillin G include most beta-hemolytic streptococci, beta-lactamase-negative staphylococci, Actinomyces species, some Bacillus anthracis, Corynebacterium species, and Erysipelothrix rhusiopathiae. Most species of anaerobes, including Clostridium species, but excluding beta-lactamase-producing Bacteroides species, are also susceptible to Penicillin G. Penicillin G is easily.id Monosodium Salt; (2S, 5R, 6R)-3, 3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Monosodium Salt; American Penicillin; Benzylpenicillin Sodium; Benzylpenicillin Sodium Salt; Benzylpenicillinic Acid Sodium Salt; Crystapen; Ethacillin; Monocillin; Monosodium Benzylpenicillin; Mycofarm; Nalpen G; Nobak; Novocillin; Pen-A-Brasive; Penicillin G Sodium; Penilaryn; Sodium 6- (Phenylacetamido) penicillanate; Sodium Benzylpenicillin; Sodium Benzylpenicillin G; Sodium Benzylpenicillinate. Grades: USP. CAS No. 69-57-8. Pack Sizes: 50g, 100g, 500g, 1Kg. Molecular Formula: C16H17N2O4NaS, Molecular Weight: 356.37. US Biological Life Sciences. | Worldwide |
| Penicillin g sulfoxide p-methoxybenzyl ester | Penicillin g sulfoxide p-methoxybenzyl ester. Group: Biochemicals. Grades: Highly Purified. CAS No. 30034-13-0. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| penicillin impurity 10 | penicillin impurity 10. Uses: For analytical and research use. CAS No. 817553-80-3. Molecular formula: C11H11NO4. Mole weight: 221.21. Catalog: APB817553803. | |
| penicillin impurity 11 | penicillin impurity 11. Uses: For analytical and research use. Molecular formula: C32H38N4O9S2. Mole weight: 686.8. Catalog: APB10858. | |
| penicillin impurity 3 | penicillin impurity 3. Uses: For analytical and research use. Molecular formula: C32H36N4O8S2. Mole weight: 668.78. Catalog: APB10854. | |
| penicillin impurity 4 | penicillin impurity 4. Uses: For analytical and research use. Molecular formula: C16H18N2O4S. Mole weight: 334.39. Catalog: APB10855. | |
| penicillin impurity 5 | penicillin impurity 5. Uses: For analytical and research use. Molecular formula: C15H21ClN2O3S. Mole weight: 344.85. Catalog: APB10856. | |
| penicillin impurity 6 | penicillin impurity 6. Uses: For analytical and research use. CAS No. 118-53-6. Molecular formula: C14H20N2O4S. Mole weight: 312.38. Catalog: APB118536. | |
| penicillin impurity 7 | penicillin impurity 7. Uses: For analytical and research use. CAS No. 4493-18-9. Molecular formula: C14H22N2O4S. Mole weight: 314.4. Catalog: APB4493189. | |
| penicillin impurity 8 | penicillin impurity 8. Uses: For analytical and research use. CAS No. 3264-88-8. Molecular formula: C16H18N2O4S. Mole weight: 334.39. Catalog: APB3264888. | |
| penicillin impurity 9 | penicillin impurity 9. Uses: For analytical and research use. Molecular formula: C16H18N2O4S. Mole weight: 334.39. Catalog: APB10857. | |
| Penicillin sodium EPimpurity D | Penicillin sodium EPimpurity D. Uses: For analytical and research use. Molecular formula: C17H19NO4S. Mole weight: 333.4. Catalog: APB10853. | |
| Penicillin sodium EPimpurity F | Penicillin sodium EPimpurity F. Uses: For analytical and research use. CAS No. 2714749-47-8. Molecular formula: C15H20N2O3S. Mole weight: 308.4. Catalog: APB2714749478. | |
| Penicillin-Streptomycin Solution (100X) | An antibacterial solution comprised of penicillin (10,000 units/ml), a beta-lactam, and streptomycin (10,000 ug/ml), an aminoglycoside in 0.9% NaCl. Synonyms: D-Streptamine, O-2-deoxy-2-(methylamino)-alpha-L-glucopyranosyl-(1-2)-O-5-deoxy-3-C-formyl-alph-L-lyxofuranosyl-(1-4)-N,N'-bis(aminoiminomethyl)-, mixt. with (2S-(2alpha,5alpha,6beta))-3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid; Penicillin G mixture with Streptomycin (1:1). CAS No. 8025-6-7. Molecular formula: C16H18N2O4S.C21H39N7O12. Mole weight: 915.96. | |
| Penicillin V | Penicillin V (Phenoxymethylpenicillin) is a potent and orally active antibiotic. Penicillin V shows antibacterial activity for Streptococci, Clostridium difficile and staphylococcus aureus. Penicillin V has the potential for the research of otitis, sinusitis, pharyngitis and tonsillitis[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Phenoxymethylpenicillin. CAS No. 87-08-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0975A. | |
| Penicillin V β-Sulfoxide-d3 | Isotope labelled Penicillin V β-Sulfoxide, an intermediate in the synthesis of Penicillin V (P223500), an antibacterial agent. Group: Biochemicals. Alternative Names: 6-Phenoxyacetamidopenici llinic Acid-d3 1 β-Oxide; Penicillin-d3 V S-Oxide; [2S-(2α,4 β,5α,6 β )]-3, 3-Dimethyl-7-oxo-6-[(phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid-d3 4-Oxide; (2S, 4S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid-d3 4-Oxide. Grades: Highly Purified. CAS No. 148680-07-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Penicillin V-d5 | Antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxy-d5-acetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid; 6-(Phenoxy-d5-acetamido)penicillanic Acid; Phenoxy methyl penicillin-d5; Phenospen-d5; Oracilline-d5; V-Cillin-d5. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Penicillin V-[d5] | A deuterated labelled Penicillin which was the first antibiotic to be used medically. Synonyms: Oracilline-d5; Phenospen-d5; V-Cillin-d5; Phenoxymethylpenicillin-d5. Grade: > 95%. CAS No. 1356837-87-0. Molecular formula: C16H13N2O5SD5. Mole weight: 355.43. | |
| Penicillin V potassium salt | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O5S. CAS No. 132-98-9. Prepack ID 55440700-25g. Molecular Weight 388.48. See USA prepack pricing. | |
| Penicillin V potassium salt | 100g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O5S. CAS No. 132-98-9. Prepack ID 55440700-100g. Molecular Weight 388.48. See USA prepack pricing. | |
| Penicillin V Potassium Salt | The Potassium Salt form of Penicillin V is an orally active penicillin that has been found to be an effective antibiotic against sorts of bacteria. Uses: Penicillins. Synonyms: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Potassium; 6-(Phenoxyacetamido)penicillanic Acid Potassium; Antibiocin; Calciopen K; Cilacil; Fenoxypen; Vepicombin; 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenoxyacetamido)-, (2S,5R,6R)-, Potassium salt. Grade: 96%. CAS No. 132-98-9. Molecular formula: C16H17KN2O5S. Mole weight: 388.48. | |
| Penicillin V Potassium Salt | Antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Potassium; 6- (Phenoxyacetamido) penicillanic Acid Potassium; Antibiocin. Grades: Highly Purified. CAS No. 132-98-9. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Penicillin x (penicillin impurity 1) | Penicillin x (penicillin impurity 1). Uses: For analytical and research use. CAS No. 525-91-7. Molecular formula: C16H18N2O5S. Mole weight: 350.39. Catalog: APB525917. | |
| Penicillin X Sodium | It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It is an antibiotic. Synonyms: (2S,5β)-6α-[[(4-Hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2β-carboxylic acid sodium salt; 6α-[(4-Hydroxyphenylacetyl)amino]penicillani cacid sodium salt; Penicillin III sodium; p-Hydroxybenzylpenicillin sodium; Benzylpenicillin Impurity C. Grade: > 95%. CAS No. 5985-13-7. Molecular formula: C16H17N2O5SNa. Mole weight: 372.37. | |
| Penicilloic V acid | Penicilloic V acid. Group: Biochemicals. Alternative Names: 4-Carboxy-5,5-dimethyl-a-[(2-phenoxyacetyl)amino]-2-thiazolidineacetic acid; (Phenoxymethyl) penicilloic acid; (Phenoxymethyl) penicilloic acid. Grades: Highly Purified. CAS No. 1049-84-9. Pack Sizes: 250mg. Molecular Formula: C16H20N2O6S. US Biological Life Sciences. | Worldwide |
| penicillopepsin | From the imperfect fungus Penicillium janthinellum. In peptidase family A1 (pepsin A family). Closely related enzymes have been isolated from P. roqueforti and P. duponti. Group: Enzymes. Synonyms: peptidase A; Penicillium janthinellum aspartic proteinase; acid protease A; Penicillium citrinum acid proteinase; Penicillium cyclopium acid proteinase; Penicillium expansum acid proteinase; Penicillium janthinellum acid proteinase; Penicillium expansum aspartic proteinase; Penicillium aspartic proteinase; Penicillium caseicolum aspartic proteinase; Penicillium roqueforti acid proteinase; Penicillium duponti aspartic proteinase; Penicillium citrinu. Enzyme Commission Number: EC 3.4.23.20. CAS No. 9074-8-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4258; penicillopepsin; EC 3.4.23.20; 9074-08-2; peptidase A; Penicillium janthinellum aspartic proteinase; acid protease A; Penicillium citrinum acid proteinase; Penicillium cyclopium acid proteinase; Penicillium expansum acid proteinase; Penicillium janthinellum acid proteinase; Penicillium expansum aspartic proteinase; Penicillium aspartic proteinase; Penicillium caseicolum aspartic proteinase; Penicillium roqueforti acid proteinase; Penicillium duponti aspartic proteinase; Penicillium citrinum aspartic proteinase. Cat No: EXWM-4258. | |
| Penicinoline | Penicinoline, an unusual quinolinone alkaloid isolated from Penicillium, has anti-malarial, insecticidal and anticancer activities. It inhibits proliferation of 95-D and HepG2 cancer cells but not HeLa, KB, KBv200 or Hep-2 cells. Synonyms: 3-carboxylic acid-2-pyrrole-4-quinolinone; 1,4-dihydro-4-oxo-2-(1H-pyrrol-2-yl)-3-quinolinecarboxylic acid; 2-(1H-Pyrrole-2-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid; marinamide; 4-oxo-2-(1H-pyrrol-2-yl)-1,4-dihydroquinoline-3-carboxylic acid. Grade: >95% by HPLC. CAS No. 1214268-60-6. Molecular formula: C14H10N2O3. Mole weight: 254.24. | |
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