compound 11b Search Results


il 17a ko apc  (Valiant Co Ltd)
93
Valiant Co Ltd il 17a ko apc
Il 17a Ko Apc, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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compound 11b  (Synaptics Inc)
90
Synaptics Inc compound 11b
Compound 11b, supplied by Synaptics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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compound 11b  (DiscoverX corporation)
90
DiscoverX corporation compound 11b
Compound 11b, supplied by DiscoverX corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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compounds 11a , 11b , 11d , 11e , and 11f  (Muegge GmbH)
90
Muegge GmbH compounds 11a , 11b , 11d , 11e , and 11f
Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / <t>11f</t> : R 1 = C 5 H 11 , R 2 = H).
Compounds 11a , 11b , 11d , 11e , And 11f, supplied by Muegge GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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compound 11b  (CEREP Inc)
90
CEREP Inc compound 11b
Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / <t>11f</t> : R 1 = C 5 H 11 , R 2 = H).
Compound 11b, supplied by CEREP Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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compounds 11b, 11c, 11e, 11h and 11i  (Verlag GmbH)
90
Verlag GmbH compounds 11b, 11c, 11e, 11h and 11i
Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / <t>11f</t> : R 1 = C 5 H 11 , R 2 = H).
Compounds 11b, 11c, 11e, 11h And 11i, supplied by Verlag GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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compounds 11a and 11b  (Janssen)
90
Janssen compounds 11a and 11b
Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / <t>11f</t> : R 1 = C 5 H 11 , R 2 = H).
Compounds 11a And 11b, supplied by Janssen, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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j compounds asoprisnil [benzaldehyde4- [(11b,17b)-17-methoxy-17-(methoxymethyl)-3oxoestra-4,9-dien-11-yl]-1-oxime  (Jenapharm GmbH Co KG)
90
Jenapharm GmbH Co KG j compounds asoprisnil [benzaldehyde4- [(11b,17b)-17-methoxy-17-(methoxymethyl)-3oxoestra-4,9-dien-11-yl]-1-oxime
Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / <t>11f</t> : R 1 = C 5 H 11 , R 2 = H).
J Compounds Asoprisnil [Benzaldehyde4 [(11b,17b) 17 Methoxy 17 (Methoxymethyl) 3oxoestra 4,9 Dien 11 Yl] 1 Oxime, supplied by Jenapharm GmbH Co KG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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atomic coordinates, bond lengths and angles, thermal parameters, and structure factors for compound 11b  (Cambridge Crystallographic)
90
Cambridge Crystallographic atomic coordinates, bond lengths and angles, thermal parameters, and structure factors for compound 11b
Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / <t>11f</t> : R 1 = C 5 H 11 , R 2 = H).
Atomic Coordinates, Bond Lengths And Angles, Thermal Parameters, And Structure Factors For Compound 11b, supplied by Cambridge Crystallographic, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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authentic standards of model compounds 11a and 11b  (Tokyo Chemical Industry)
90
Tokyo Chemical Industry authentic standards of model compounds 11a and 11b
Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / <t>11f</t> : R 1 = C 5 H 11 , R 2 = H).
Authentic Standards Of Model Compounds 11a And 11b, supplied by Tokyo Chemical Industry, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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compounds 8b–11 b  (Verlag GmbH)
90
Verlag GmbH compounds 8b–11 b
Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / <t>11f</t> : R 1 = C 5 H 11 , R 2 = H).
Compounds 8b–11 B, supplied by Verlag GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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x-ray structure of humanised murine 11b-hsd1 in complex with compound 22  (Proteros Biostructures)
90
Proteros Biostructures x-ray structure of humanised murine 11b-hsd1 in complex with compound 22
Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / <t>11f</t> : R 1 = C 5 H 11 , R 2 = H).
X Ray Structure Of Humanised Murine 11b Hsd1 In Complex With Compound 22, supplied by Proteros Biostructures, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / 11f : R 1 = C 5 H 11 , R 2 = H).

Journal: International Journal of Molecular Sciences

Article Title: Naphthoquinone-Quinolone Hybrids with Antitumor Effects on Breast Cancer Cell Lines—From the Synthesis to 3D-Cell Culture Effects

doi: 10.3390/ijms25126490

Figure Lengend Snippet: Synthetic route towards 1,4-naphthoquinone/4-quinolone conjugates. a: (1) EMME, EtOH; (2) Diphenylether, 250 °C; b: (1) K 2 CO 3 , DMF, r. t., 15 min. (2) R1-X, DMF, 80 °C, 24 h.; c: H 2 (20 bar), Pd/C (10%), EtOH, 50 °C, 3 h. (for R1 = ethyl and pentyl); d: NH 4 Cl 0,05 M, Fe, reflux (for R1 = benzyl); e: (1) NaOH, EtOH, r. t. (2) H 2 O, HCl; f: t-butyl nitrite, DMSO, H 2 O, 1,4-naphthoquinone, ultrasound, 25 °C. ( 15a/11a : R 1 = Et, R 2 = Et; 15b/11b : R 1 = Bn, R 2 = Et; 15c / 11c : R 1 = Pentyl, R 2 = Et; 16a / 11d : R 1 = Et, R 2 = H; 16b / 11e : R 1 = CH 2 C 6 H 5 , R 2 = H; 16c / 11f : R 1 = C 5 H 11 , R 2 = H).

Article Snippet: Additionally, compounds 11a , 11b , 11d , 11e , and 11f exhibited zero violations of the drug-likeness rules of Lipinski, Ghose, Veber, Egan, and Muegge.

Techniques: Reflux

IC 50 values and selectivity indices (SI) of 1,4-naphthoquinone, compounds 11a–f , and doxorubicin.

Journal: International Journal of Molecular Sciences

Article Title: Naphthoquinone-Quinolone Hybrids with Antitumor Effects on Breast Cancer Cell Lines—From the Synthesis to 3D-Cell Culture Effects

doi: 10.3390/ijms25126490

Figure Lengend Snippet: IC 50 values and selectivity indices (SI) of 1,4-naphthoquinone, compounds 11a–f , and doxorubicin.

Article Snippet: Additionally, compounds 11a , 11b , 11d , 11e , and 11f exhibited zero violations of the drug-likeness rules of Lipinski, Ghose, Veber, Egan, and Muegge.

Techniques:

Physicochemical parameter values for compounds 11a–f using Swiss ADME server.

Journal: International Journal of Molecular Sciences

Article Title: Naphthoquinone-Quinolone Hybrids with Antitumor Effects on Breast Cancer Cell Lines—From the Synthesis to 3D-Cell Culture Effects

doi: 10.3390/ijms25126490

Figure Lengend Snippet: Physicochemical parameter values for compounds 11a–f using Swiss ADME server.

Article Snippet: Additionally, compounds 11a , 11b , 11d , 11e , and 11f exhibited zero violations of the drug-likeness rules of Lipinski, Ghose, Veber, Egan, and Muegge.

Techniques: