Indole Building Blocks

An article A Thieno[2,3-d]pyrimidine Scaffold Is a Novel Negative Allosteric Modulator of the Dopamine D-2 Receptor WOS:000455561400011 published article about LIGAND DISCOVERY; D-3; PHARMACOLOGY; SELECTIVITY; INHIBITORS; SB269652; D2 in [Fyfe, Tim J.; Scammells, Peter J.; Capuano, Ben] Monash Univ, Med Chem, Monash Inst Pharmaceut Sci, Parkville, Vic 3052, Australia; [Fyfe, Tim J.; Lim, Herman D.; Lane, J. Robert] Monash Univ, Monash Inst Pharmaceut Sci, Drug Discovery Biol, Parkville, Vic 3052, Australia; [Fyfe, Tim J.; Kellam, Barrie; Mistry, Shailesh N.] Univ Nottingham, Ctr Biomol Sci, Sch Pharm, Nottingham NG7 2RD, England; [Zarzycka, Barbara; Katrich, Vsevolod] Univ Southern Calif, Bridge Inst, Dept Biol Sci, Los Angeles, CA 90089 USA; [Katrich, Vsevolod] Univ Southern Calif, Bridge Inst, Dept Chem, Los Angeles, CA 90089 USA in 2019, Cited 41. Category: indole-building-block. The Name is 3-(Trifluoromethyl)phenol. Through research, I have a further understanding and discovery of 98-17-9

Recently, a novel negative allosteric modulator (NAM) of the D-2-like dopamine receptors 1 was identified through virtual ligand screening. This ligand comprises a thieno[2,3-d]pyrimidine scaffold that does not feature in known dopaminergic ligands. Herein, we provide pharmacological validation of an allosteric mode of action for 1, revealing that it is a NAM of dopamine efficacy and identify the structural determinants of this allostery. We find that key structural moieties are important for functional affinity and negative cooperativity, while functionalization of the thienopyrimidine at the 5- and 6-positions results in analogues with divergent cooperativity profiles. Successive compound iterations have yielded analogues exhibiting a 10-fold improvement in functional affinity, as well as enhanced negative cooperativity with dopamine affinity and efficacy. Furthermore, our study reveals a fragment-like core that maintains low mu M affinity and robust negative cooperativity with markedly improved ligand efficiency.

About 3-(Trifluoromethyl)phenol, If you have any questions, you can contact Fyfe, TJ; Zarzycka, B; Lim, HD; Kellam, B; Mistry, SN; Katrich, V; Scammells, PJ; Lane, JR; Capuano, B or concate me.. Category: indole-building-block

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Reddy, VG; Jampaiah, D; Chalkidis, A; Sabri, YM; Mayes, ELH; Bhargava, SK in [Reddy, Velma Ganga; Jampaiah, Deshetti; Chalkidis, Anastasios; Sabri, Ylias M.; Bhargava, Suresh K.] RMIT Univ, Sch Sci, CAMIC, GPO Box 2476, Melbourne, Vic 3001, Australia; [Mayes, Edwin L. H.] RMIT Univ, RMMF, GPO Box 2476, Melbourne, Vic 3001, Australia published Highly dispersed cobalt oxide nanoparticles on manganese oxide nanotubes for aerobic oxidation of benzyl alcohol in 2019.0, Cited 34.0. Formula: C7H8O. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6.

Hybrid Co3O4/MnO2 nanotube-based catalysts were prepared by a simple hydrothermal synthesis method. The physico-chemical properties of Co3O4/MnO2 catalyst were then studied by different characterization techniques, namely, SEM, TEM and HR-TEM, XRD, BET surface area, XPS and H-2-TPR. The hybrid catalyst showed superior catalytic performance toward benzyl alcohol oxidation than pure MnO2 nanotubes and Co3O4 nanoparticles. The uniform dispersion of Co3O4 nanoparticles, good redox behaviour, the variable oxidation states of manganese and cobalt (Mn3+/4+ or Co3+/2+) as well as the abundance of active surface oxygen species were responsible for such a high catalytic activity.

About Benzyl Alcohol, If you have any questions, you can contact Reddy, VG; Jampaiah, D; Chalkidis, A; Sabri, YM; Mayes, ELH; Bhargava, SK or concate me.. Formula: C7H8O

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Recently I am researching about PHARMACOKINETICS; ANESTHESIA; SAFETY, Saw an article supported by the Key Research AMP; Development Projects of the Department of Science AMP; Technology of Sichuan Province [2019YFS0093]. HPLC of Formula: C7H8O. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Liu, LQ; Hong, PX; Song, XH; Zhou, CC; Ling, R; Kang, Y; Qi, QR; Yang, J. The CAS is 100-51-6. Through research, I have a further understanding and discovery of Benzyl Alcohol

In this work, a series of water-soluble propofol prodrugs were synthesized, and their propofol release rate and pharmacodynamic characteristics were measured. We found that inserting glycolic acid as a linker between propofol and the cyclic amino acid accelerated the release of propofol from prodrugs into the plasma while preserving its safety. In animal experiments, prodrugs (3e, 3g, and 3j) were significantly better than fospropofol (the only water-soluble propofol prodrug that has been used clinically) in terms of safety, onset, and duration time of anesthesia. Their molar dose, onset time, and anesthesia duration time were comparable to those of propofol, helping to maintain the clinical benefits of propofol. The experimental results showed the potential of such compounds as water-soluble prodrugs of propofol.

HPLC of Formula: C7H8O. About Benzyl Alcohol, If you have any questions, you can contact Liu, LQ; Hong, PX; Song, XH; Zhou, CC; Ling, R; Kang, Y; Qi, QR; Yang, J or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Authors Gein, VL; Pastukhova, EV in MAIK NAUKA/INTERPERIODICA/SPRINGER published article about in [Gein, V. L.; Pastukhova, E. V.] Perm State Pharmaceut Acad, Perm 614990, Russia in 2021, Cited 5. HPLC of Formula: C8H8O2. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

A series of new 1-aminocarbonylmethyl-5-aryl-4-aroyl-3-hydroxy-3-pyrrolin-2-ones has been synthesized through a three-component reaction of aroylpyruvic acid methyl ester with a mixture of aromatic aldehyde and glycinamide hydrochloride in glacial acetic acid in the presence of anhydrous sodium bicarbonate.

HPLC of Formula: C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Gein, VL; Pastukhova, EV or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Thermal Coursed Effect of Comprehensive Changes in the Flavor/Taste of Cynanchi wilfordii WOS:000488796100001 published article about TONGUE; NOSE in [Kim, Da-som; Lee, Jookyeong Tracy; Hong, Seong Jun; Cho, Jin-Ju; Shin, Eui-Cheol] Gyeongnam Natl Univ Sci & Technol, Dept Food Sci, Jinju 52725, South Korea in 2019.0, Cited 32.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. Quality Control of 4′-Hydroxyacetophenone

This study aims to investigate alterations in volatile compounds and chemical components that may affect the sensory properties of Cynanchi wilfordii roasted at 120 degrees C and 180 degrees C for various durations of time (0 to 4 min). For volatile compound profiles, tridecane, tetradecane, and ethyl hexyl ether were detected as major compounds of the sample without roasting. As the roasting temperature increased, the types of volatile compounds increased, whereas the content decreased with an increase in heterocyclic compound generation. The sample roasted at 120 degrees C for 1 min showed a notably different profile pattern from the other roasted samples. For the sniffing test performed by trained panelists using gas chromatography olfactometry, naphthalene and nonanal, which induce spicy and raw C. wilfordii, respectively, were perceived most intensely throughout all the samples. In the electronic tongue analysis, the sample roasting at 180 degrees C showed an increased and decreased pattern in umami taste and saltiness, respectively, with increased roasting time. Electronic tongue analysis results showed that the sample roasted at 180 degrees C for 4 min would have the best sensory preference. Along with the volatile compound profiles, the sample roasted at 120 degrees C for 1 min had more sourness than the other samples, and would potentially have distinctive sensory characteristics. This study should provide baseline data on variations in the sensory properties and industrial applications of C. wilfordii upon roasting. Practical Application Various applications of food ingredients through changes in sensory characteristics by roasting will provide consumers more options for food selections. Accordingly, this study will be utilized by (1) individuals and food companies who are interested in functional foods, (2) individuals and food industries that seek optimum roasting conditions for proper sensory characteristics of foods, and (3) farmers and crop producers who seek for utilization the applications of Cynanchi wilfordii as a food ingredient.

About 4′-Hydroxyacetophenone, If you have any questions, you can contact Kim, DS; Lee, JT; Hong, SJ; Cho, JJ; Shin, EC or concate me.. Quality Control of 4′-Hydroxyacetophenone

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article A new antifungal aminobenzamide derivative from the endophytic fungus Fusarium sp. WOS:000468924000005 published article about TETRACYCLIC TRITERPENOIDS; FUSARITHIOAMIDE; BUTYROLACTONES in [Ibrahim, Sabrin R. M.; Al Haidari, Rwaida A.; Zayed, Mohamed F.] Taibah Univ, Coll Pharm, Dept Pharmacognosy & Pharmaceut Chem, Al Madinah Al Munawwarah, Saudi Arabia; [Ibrahim, Sabrin R. M.] Assiut Univ, Fac Pharm, Dept Pharmacognosy, Assiut, Egypt; [Mohamed, Gamal A.] King Abdulaziz Univ, Fac Pharm, Dept Nat Prod & Alternat Med, Jeddah, Saudi Arabia; [Mohamed, Gamal A.] Al Azhar Univ, Assiut Branch, Fac Pharm, Dept Pharmacognosy, Assiut, Egypt; [Khayat, Maan T.] King Abdulaziz Univ, Fac Pharm, Dept Pharmaceut Chem, Jeddah, Saudi Arabia; [El-Kholy, Amal A.] Taibah Univ, Coll Pharm, Dept Clin & Hosp Pharm, Al Madinah Al Munawwarah, Saudi Arabia; [El-Kholy, Amal A.] Ain Shams Univ, Dept Clin Pharm, Fac Pharm, Cairo, Egypt; [Zayed, Mohamed F.] Al Azhar Univ, Dept Pharmaceut Chem, Fac Pharm, Cairo, Egypt in 2019.0, Cited 17.0. Quality Control of 4′-Hydroxyacetophenone. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4

Background: Endophytic fungi attracted attention as a prolific source of bioactive natural products with a potent pharmaceutical activity and unique structure. Objective: The main goal of the study is to separate and identify the bioactive constituents from the endophytic fungus Fusarium sp. as well as to evaluate the antimicrobial of the new metabolites. Materials and Methods: The fungus was cultured on a rice medium, and then, the cultures were extracted with ethyl acetate (EtOAc). The EtOAc extract was chromatographed utilizing different chromatographic methods to give five metabolites. The structural determination of these metabolites was carried out by the analyses of various spectroscopic data, in addition to comparison with the formerly reported data. The antifungal and antibacterial potentials were evaluated toward various microbial strains using disc diffusion assay. Results: A new aminobenzamide derivative, namely fusaribenzamide A (2), and four known metabolites: (22E,24R)-stigmasta-5,7,22-trien-3–ol (1), adenosine (3), p-hydroxyacetophenone (4), and tyrosol (5) were isolated. Fusaribenzamide A (2) possessed significant antifungal activity toward Candida albicans with minimum inhibitory concentration (MIC) value 11.9 mg/disc compared to nystatin (MIC 4.9 mg/disc). Conclusion: The endophytic fungus Fusarium sp. could be considered as a wealthy pool for the isolation of aminobenzamide derivatives. Fusaribenzamide A may be a candidate for the discovery of a promising antifungal agent.

Quality Control of 4′-Hydroxyacetophenone. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Ibrahim, SRM; Mohamed, GA; Khayat, MT; Al Haidari, RA; El-Kholy, AA; Zayed, MF or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Computed Properties of C7H8O2. Authors Shen, J; Li, QW; Zhang, XY; Wang, X; Li, GZ; Li, WZ; Yang, SD; Yang, B in AMER CHEMICAL SOC published article about in [Shen, Jian; Li, Qi-Wei; Zhang, Xin-Yue; Wang, Xue; Li, Gui-Zhi; Li, Wen-Zuo; Yang, Bin] Yantai Univ, Coll Chem & Chem Engn, Yantai 264005, Peoples R China; [Yang, Shang-Dong] Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China in 2021, Cited 112. The Name is Mequinol. Through research, I have a further understanding and discovery of 150-76-5

A Tf2O/DMSO-based system for the dehydrogenative coupling of a wide range of alcohols, phenols, thiols, and thiophenols with diverse phosphorus reagents has been developed. This metal- and strong-oxidant-free strategy provides a facile approach to a great variety of organophosphinates and thiophosphates. The simple reaction system, good functional-group tolerance, and broad substrate scope enable the application of this method to the modification of natural products and the direct synthesis of bioactive molecules and flame retardants.

Computed Properties of C7H8O2. About Mequinol, If you have any questions, you can contact Shen, J; Li, QW; Zhang, XY; Wang, X; Li, GZ; Li, WZ; Yang, SD; Yang, B or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Formula: C7H8O. I found the field of Chemistry; Materials Science very interesting. Saw the article Facile synthesis of hydrothermally stable mesoporous ZSM-5 zeolite from Al- SBA-16 via steam assisted crystallization published in 2020, Reprint Addresses Cheralathan, KK (corresponding author), VIT, Sch Adv Sci, Dept Chem, Vellore 632014, Tamil Nadu, India.. The CAS is 100-51-6. Through research, I have a further understanding and discovery of Benzyl Alcohol.

In this work, Al grafted SBA-16 (Al-SBA-16) is converted into a fully crystalline hierarchical mesoporous ZSM-5 zeolite with hydrothermal stability by steam assisted crystallization under controlled conditions. The secondary mesoporosity is due to reorganization and recrystallization events happening upon steaming the precursor. Two mesoporous aluminosilicates (Al-SBA-16s) are used as the precursors of zeolites. The precursors are obtained by post-synthetic Al grafting on the silica walls of SBA-16 with aluminium isopropoxide and sodium aluminate. Mesoporous ZSM-5 zeolites obtained from the Al-SBA-16 precursors and commercial ZSM-5 are characterized using XRD, XRF, FT-IR, TEM, N-2 adsorption, Al-27 and Si-29 MAS NMR, and TPD of NH3. The results indicated the presence of intraparticle mesoporosity in the prepared mesoporous zeolites and they have comparable crystallinity with commercial ZSM-5. Catalytic activity of the synthesized mesoporous zeolites in benzylation of mesitylene is found to be comparatively more than commercial ZSM-5, which shows existence of micro/meso hierarchical structure in the mesoporous ZSM-5 zeolites. The aluminium sources, aluminium isopropoxide and sodium aluminate have a remarkable influence on the textural, acidity, and hydrothermal stability characteristics of the synthesized mesoporous ZSM-5 zeolites.

About Benzyl Alcohol, If you have any questions, you can contact Kamil, MSM; Cheralathan, KK or concate me.. Formula: C7H8O

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Synthesis, in vitro evaluation and molecular docking of new pyrazole derivatives bearing 1,5,10,10a-tetrahydrobenzo[g]quinoline-3-carbonitrile moiety as potent antibacterial agents WOS:000580977100002 published article about ANTIMICROBIAL ACTIVITY; ANALGESIC ACTIVITY; HETEROCYCLES in [Elkanzi, Nadia A. A.; Alruwaili, May M.; Alruwaili, Enas D.; Almamtrfi, Rahaf W.; Alsharary, Hadeel Kh.] Jouf Univ, Coll Sci, Chem Dept, POB 2014, Sakaka, Saudi Arabia; [Elkanzi, Nadia A. A.] Aswan Univ, Fac Sci, Chem Dept, POB 81528, Aswan, Egypt; [Hrichi, Hajer] Carthage Univ, Ctr Urbain Nord, Natl Inst Appl Sci & Technol, BPN 676, Tunis 1080, Tunisia; [Bakr, Rania B.; Hendawy, O.] Jouf Univ, Coll Pharm, Dept Pharmacol, Sakaka 2014, Aljouf, Saudi Arabia; [Bakr, Rania B.] Beni Suef Univ, Fac Pharm, Dept Pharmaceut Organ Chem, Bani Suwayf 62514, Egypt; [Hendawy, O.] Beni Suef Univ, Fac Med, Dept Clin Pharmacol, Bani Suwayf, Egypt in 2021, Cited 34. Product Details of 123-11-5. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

In the current study, a new series of pyrazole derivatives4a-d,5a-dand6a-dpossessing 1,5,10,10a-tetrahydrobenzo[g]quinoline-3-carbonitrile moiety were synthesized by treating chalcones (3a-d) with hydrazine monohydrate/acetic anhydride, hydrazine monohydrate/formic acid and 4-chlorophenylhydrazine in ethanol, respectively. These reactions proceeded smoothly with satisfactory yields, and the obtained compounds were characterized using FTIR,H-1-NMR,C-13-NMR and elemental analyses. All the synthesized compounds were subjected to antibacterial activity againstBacillus subtilis,Staphylococcus aureus,Escherichia coli, andPseudomonas aeruginosabacteria and molecular docking studies. The antibacterial studies showed that all compounds exhibited good to excellent antibacterial activity against the tested bacterial strains. The structure-activity relationship studies revealed that the compounds3b,4b,5band6bbearing a chlorine atom at the para position of the phenyl group attached to pyrazole moiety in displayed the highest antibacterial activity against all the tested bacteria exceeding the standard drug ampicillin. Moreover, the molecular docking results showed that the highest scores docking have been obtained from the most active antibacterial compounds3b,3d,4b,4d,4c,5band6bwith good energy binding score within the active site of topoisomerase II DNA gyrase enzymes (PDB ID: 2XCS), suggesting that they can act by the inhibition of DNA replication. These compounds are auspicious candidates as antibacterial agents that would deserve further investigations.

Product Details of 123-11-5. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Elkanzi, NAA; Hrichi, H; Bakr, RB; Hendawy, O; Alruwaili, MM; Alruwaili, ED; Almamtrfi, RW; Alsharary, HK or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Pictet-Spengler condensations using 4-(2-aminoethyl)coumarins WOS:000558066500020 published article about RESISTANT PROSTATE-CANCER; ANDROGEN RECEPTOR; DIHYDROTESTOSTERONE; TARGET; INHIBITORS; ANDROSTANEDIOL; DEHYDROGENASES; IDENTIFICATION; TESTOSTERONE; BIOCHEMISTRY in [Sviripa, Vitaliy M.; Williams, Alexander H.; Zhan, Chang-Guo] Univ Kentucky, Coll Pharm, Dept Pharmaceut Sci, Lexington, KY 40536 USA; [Sviripa, Vitaliy M.; Begley, Kristin L.; Wyrebek, Przemyslaw; Kril, Liliia M.; Balia, Andrii G.; Zhan, Chang-Guo; Watt, David S.] Univ Kentucky, Coll Pharm, Ctr Pharmaceut Res & Innovat, Lexington, KY 40536 USA; [Sviripa, Vitaliy M.; Liu, Chunming; Watt, David S.] Univ Kentucky, Lucille Parker Markey Canc Ctr, Lexington, KY 40536 USA; [Fiandalo, Michael, V; Mohler, James L.] Roswell Pk Comprehens Canc Ctr, Dept Expt Therapeut, Buffalo, NY 14263 USA; [Begley, Kristin L.; Wyrebek, Przemyslaw; Kril, Liliia M.; Balia, Andrii G.; Liu, Chunming; Watt, David S.] Univ Kentucky, Coll Med, Dept Mol & Cellular Biochem, Lexington, KY 40536 USA; [Parkin, Sean R.] Univ Kentucky, Coll Arts & Sci, Dept Chem, Lexington, KY 40506 USA; [Subramanian, Vivekanandan] Univ Kentucky, Coll Pharm, NMR Ctr, Lexington, KY 40536 USA; [Chen, Xi] South Cent Univ Nationalities, Coll Chem & Mat Sci, Wuhan 430074, Peoples R China; [Mohler, James L.] Roswell Pk Comprehens Canc Ctr, Dept Urol, Buffalo, NY 14263 USA in 2020.0, Cited 57.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6. Product Details of 150-19-6

Androgen-deprivation therapy (ADT) is only a palliative measure, and prostate cancer invariably recurs in a lethal, castration-resistant form (CRPC). Prostate cancer resists ADT by metabolizing weak, adrenal androgens to growth-promoting 5 alpha-dihydrotestosterone (DHT), the preferred ligand for the androgen receptor (AR). Developing small-molecule inhibitors for the final steps in androgen metabolic pathways that utilize 17-oxidoreductases required probes that possess fluorescent groups at C-3 and intact, naturally occurring functionality at C-17. Application of the Pictet-Spengler condensation to substituted 4-(2-aminoethyl)coumarins and 5 alpha-androstane-3-ones furnished spirocyclic, fluorescent androgens at the desired C-3 position. Condensations required the presence of activating C-7 amino orN,N-dialkylamino groups in the 4-(2-aminoethyl)coumarin component of these condensation reactions. Successful Pictet-Spengler condensation, for example, of DHT with 9-(2-aminoethyl)-2,3,6,7-tetrahydro-1H,5H,11H-pyrano[2,3-f]pyrido[3,2,1-ij]quinolin-11-one led to a spirocyclic androgen, (3R,5S,10S,13S,17S)-17-hydroxy-10,13-dimethyl-1,2,2 ‘,3 ‘,4,5,6,7,8,8 ‘,9,9 ‘,10,11,12,12 ‘,13,13 ‘,14,15,16,17-docosahydro-7 ‘ H,11 ‘ H-spiro-[cyclopenta[a]phenanthrene-3,4 ‘-pyrido[3,2,1-ij]pyrido[4 ‘,3 ‘:4,5]pyrano[2,3-f]quinolin]-5 ‘(1 ‘ H)-one. Computational modeling supported the surrogacy of the C-3 fluorescent DHT analog as a tool to study 17-oxidoreductases for intracrine, androgen metabolism.

Product Details of 150-19-6. About m-Methoxyphenol, If you have any questions, you can contact Sviripa, VM; Fiandalo, MV; Begley, KL; Wyrebek, P; Kril, LM; Balia, AG; Parkin, SR; Subramanian, V; Chen, X; Williams, AH; Zhan, CG; Liu, CM; Mohler, JL; Watt, DS or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles