Assay ID | Title | Year | Journal | Article |
AID40215 | Antimicrobial activity on Bacillus cereus | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID247972 | In vitro antiproliferative activity against murine leukemia L1210 cells | 2005 | Journal of medicinal chemistry, Mar-10, Volume: 48, Issue:5
| Synthesis and biological evaluation of novel naphthocarbazoles as potential anticancer agents. |
AID164640 | Inhibition of Protein Kinase A (PKA). | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID135924 | Antitumor activity against mice with B16 melanoma was assessed from the ratio of median survival time of treated animals (T) to controls animals, at 64 mg/Kg | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID40213 | Antimicrobial activity against Bacillus cereus | 1997 | Journal of medicinal chemistry, Oct-10, Volume: 40, Issue:21
| Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. |
AID210944 | Inhibition of calf thymus Topoisomerase-I | 1997 | Journal of medicinal chemistry, Oct-10, Volume: 40, Issue:21
| Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. |
AID361673 | Anticancer activity against human K562 cells | 2008 | Bioorganic & medicinal chemistry, Aug-15, Volume: 16, Issue:16
| A concise approach to 1,11-didechloro-6-methyl-4'-O-demethyl rebeccamycin and its binding to human serum albumin: fluorescence spectroscopy and molecular modeling method. |
AID163166 | Inhibition of Protein kinase C alpha | 1997 | Journal of medicinal chemistry, Oct-10, Volume: 40, Issue:21
| Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. |
AID139421 | In vivo efficacy study on mice with P388 Leukemia Cells determined after administration of 2 mg/kg/day dosage | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID155030 | Compound was tested for drug bound to cell pellet (P388 leukemia) after centrifugation at 320 nm. | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID152986 | Ratio of IC50 of p388 and p388CPT5 cell lines | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID209054 | Antimicrobial activity against gram-positive Streptococcus chartreusis NRRL 11407 was determined by antibiogram test.++ means growth inhibition zone was 8-9 mm. | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID139418 | In vivo efficacy study on mice with B16 Melanoma cells determined after administration of 2 mg/kg/day dosage | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID57052 | Inhibitory activity towards Topoisomerase 2 from calf thymus | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID56700 | Inhibitory activity towards Topoisomerase 1 from calf thymus. | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID235711 | Selectivity was measured [Selectivity = (CC50/IC50) against HIV-1 infected CEM-SS cells] | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID154139 | In vitro inhibitory concentration against murine P388CPT5 leukemia cell proliferation | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID247635 | Inhibitory concentration against K5662 leukemia cell line in MTS assay | 2005 | Journal of medicinal chemistry, Apr-07, Volume: 48, Issue:7
| Syntheses and biological activities of rebeccamycin analogues with uncommon sugars. |
AID39123 | Inhibition of murine B16 Melanoma cell proliferation | 1997 | Journal of medicinal chemistry, Oct-10, Volume: 40, Issue:21
| Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. |
AID8281 | Antiproliferative activity in vitro against A549 (human non-small lung carcinoma) cell line. | 2002 | Journal of medicinal chemistry, Mar-14, Volume: 45, Issue:6
| Syntheses and antiproliferative activities of new rebeccamycin derivatives with the sugar unit linked to both indole nitrogens. |
AID235560 | Selectivity Index (SI) refers to the ratio of the anti HIV activities CC50/IC50 in HIV-1 Lai infected CEM-SS cells. | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID45186 | The cytotoxicity was evaluated in in HIV -I Lai infected CEM-SS cells. | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID45177 | Cytotoxicity against HIV-1 Lai infected CEM-SS cells | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID39106 | Antiproliferative activity against B16 mouse melanoma cells | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID208030 | In Vitro growth inhibitory effect of compounds against Gram-Positive Bacteria Streptomyces chartreusis NRRL11407 | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID46218 | Cytotoxic concentration is tested against CEM-SS cells | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID40214 | Antimicrobial activity is tested against Bacillus cereus | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID165270 | Inhibition of protein kinase C (PKC) | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID139417 | In vivo efficacy study on mice with B16 Melanoma cells determined after administration of 16 mg/kg/day dosage | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID38066 | Antiproliferative activity measured against murine B16 melanoma cells | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID150379 | Antiproliferative activity against P388 Murine Leukemia cells | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID494538 | Cytotoxicity activity against human DU145 cells by MTT assay | 2010 | Bioorganic & medicinal chemistry letters, Aug-01, Volume: 20, Issue:15
| Synthesis and biological evaluation of novel benzodioxinocarbazoles (BDCZs) as potential anticancer agents. |
AID152507 | Compound was tested for drug bound to whole cells (P388 leukemia) before centrifugation at 320 nm. | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID96457 | Antiproliferative activity tested in vitro against L1210 (murine leukemia) cell line. | 2002 | Journal of medicinal chemistry, Mar-14, Volume: 45, Issue:6
| Syntheses and antiproliferative activities of new rebeccamycin derivatives with the sugar unit linked to both indole nitrogens. |
AID95647 | Antiproliferative activity in vitro against K-562 (human leukemia) cell line. | 2002 | Journal of medicinal chemistry, Mar-14, Volume: 45, Issue:6
| Syntheses and antiproliferative activities of new rebeccamycin derivatives with the sugar unit linked to both indole nitrogens. |
AID211126 | Inhibition of calf thymus Topoisomerase-2 | 1997 | Journal of medicinal chemistry, Oct-10, Volume: 40, Issue:21
| Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. |
AID135923 | Antitumor activity against mice with B16 melanoma was assessed from the ratio of median survival time of treated animals (T) to controls animals, at 2 mg/Kg | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID150511 | Cytotoxicity against P388 leukemia cells | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID135925 | Antitumor activity against mice with P388 leukemia cell was assessed from the ratio of median survival time of treated animals (T) to controls animals, at 16 mg/Kg | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID135926 | Antitumor activity against mice with P388 leukemia cell was assessed from the ratio of median survival time of treated animals (T) to controls animals, at 2 mg/Kg | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID40204 | Antimicrobial activity against gram-positive Bacillus cereusATCC 14579 was determined by antibiogram test.++ means growth inhibition zone was 8-9 mm. | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID211110 | Compound was tested for anti microbial activity against topoisomerase I. | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID153542 | Cytotoxicity against P388/CPT5 leukemia cells. | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID165134 | Inhibition of Protein Kinase C(PKC) | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID46072 | Selective Index of against HIV -I Lai infected CEM-SS cells. | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID135922 | Antitumor activity against mice with B16 melanoma was assessed from the ratio of median survival time of treated animals (T) to controls animals, at 16 mg/Kg | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID154138 | Antiproliferative activity measured against P388CPT5 cells resistant to Topoisomerase I inhibitor Camptothecin | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID55322 | Variation in melting temperature (delta Tm) of helix-to-coil transition of DNA was reported. | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID155031 | Fraction change in percent is observed. | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID361672 | Anticancer activity against human SW620 cells | 2008 | Bioorganic & medicinal chemistry, Aug-15, Volume: 16, Issue:16
| A concise approach to 1,11-didechloro-6-methyl-4'-O-demethyl rebeccamycin and its binding to human serum albumin: fluorescence spectroscopy and molecular modeling method. |
AID135927 | Antitumor activity against mice with P388 leukemia cell was assessed from the ratio of median survival time of treated animals (T) to controls animals, at 64 mg/Kg | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID247867 | Inhibitory concentration against SW620 colorectal carcinoma cell line in MTS assay | 2005 | Journal of medicinal chemistry, Apr-07, Volume: 48, Issue:7
| Syntheses and biological activities of rebeccamycin analogues with uncommon sugars. |
AID494537 | Cytotoxicity activity against mouse L1210 cells by MTT assay | 2010 | Bioorganic & medicinal chemistry letters, Aug-01, Volume: 20, Issue:15
| Synthesis and biological evaluation of novel benzodioxinocarbazoles (BDCZs) as potential anticancer agents. |
AID151244 | Antiproliferative activity measured against P388 Leukemia cells | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID40327 | Minimum inhibitory concentration against gram-positive Bacillus cereus | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID56701 | Minimum inhibitory concentration against DNA topoisomerase I | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID235100 | Resistance Index (RI) refers to the ratio of the [IC50 (P388/CPT5)] / IC50 P388. | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID139420 | In vivo efficacy study on mice with P388 Leukemia Cells determined after administration of 16 mg/kg/day dosage | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID211093 | Inhibition of human Topoisomerase I | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID150657 | In vitro inhibitory concentration against murine P388 leukemia cell proliferation | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID40208 | In Vitro growth inhibitory effect of compounds against Gram-Positive Bacteria Bacillus cereus ATCC 14579 | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID40318 | Compound was tested for antimicrobial activity against a gram-positive bacterium Bacillus cereus | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID150519 | Inhibition of P388 murine leukemia cell proliferation | 1997 | Journal of medicinal chemistry, Oct-10, Volume: 40, Issue:21
| Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. |
AID84287 | Antiproliferative activity in vitro against HT-29 (human colon carcinoma) cell line. | 2002 | Journal of medicinal chemistry, Mar-14, Volume: 45, Issue:6
| Syntheses and antiproliferative activities of new rebeccamycin derivatives with the sugar unit linked to both indole nitrogens. |
AID248432 | In vitro antiproliferative activity against human prostate cancer DU145 cells; not determined | 2005 | Journal of medicinal chemistry, Mar-10, Volume: 48, Issue:5
| Synthesis and biological evaluation of novel naphthocarbazoles as potential anticancer agents. |
AID248062 | In vitro antiproliferative activity against human colon carcinoma HT-29 cells | 2005 | Journal of medicinal chemistry, Mar-10, Volume: 48, Issue:5
| Synthesis and biological evaluation of novel naphthocarbazoles as potential anticancer agents. |
AID45880 | Anti-HIV-1 activity in CEM-SS cells was measured by the quantification of the reverse transcriptase activity, associated with the virus particles released from HIV-1 infected cells in the culture medium. | 1999 | Journal of medicinal chemistry, Feb-25, Volume: 42, Issue:4
| Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. |
AID46452 | Inhibitory concentration is tested in HIV-1 Lai-infected CEM-SS cells | 1998 | Journal of medicinal chemistry, May-07, Volume: 41, Issue:10
| Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. |
AID45899 | Compound was tested for anti-HIV activity in HIV -I Lai infected CEM-SS cells. | 1999 | Journal of medicinal chemistry, May-20, Volume: 42, Issue:10
| Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. |
AID139422 | In vivo efficacy study on mice with P388 Leukemia Cells determined after administration of 64 mg/kg/day dosage | 1996 | Journal of medicinal chemistry, Oct-25, Volume: 39, Issue:22
| Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. |
AID96451 | Effect on the cell cycle of L1210 cells and expressed as percent of L1210 cells in G2+M phases at 1 uM concentration | 2002 | Journal of medicinal chemistry, Mar-14, Volume: 45, Issue:6
| Syntheses and antiproliferative activities of new rebeccamycin derivatives with the sugar unit linked to both indole nitrogens. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |