Chemical Formula: C34H26O8

Chemical Formula C34H26O8

Found 22 metabolite its formula value is C34H26O8

Albanol A

Mulberrofuran G

C34H26O8 (562.1627596000001)


Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM[2]. Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM[2]. Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM[2].

   

Vialinin A

4,4",5,6-tetrahydroxy[1,1:4,1"-terphenyl]-2,3-diyl ester benzeneacetic acid

C34H26O8 (562.1627596000001)


   
   
   
   
   
   
   
   

Mulberrofuran_G

3aH-Benzo[3,4][2]benzopyrano[1,8-bc][1]-benzopyran-4,11-diol, 8a-(2,4-dihydroxphenyl)-1,8a,13b,13c-tetrahydro-6-(6-hydroxy-2-benzofuranyl)-2-methyl-, (3a,S,8aS,13bS,13cR)-

C34H26O8 (562.1627596000001)


1-(2,4-Dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,11,14,16,18-heptaene-5,15-diol is a natural product found in Morus lhou, Morus alba, and Broussonetia with data available. Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM[2]. Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM[2]. Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM[2].

   

Mulberrofuran G

Mulberrofuran G

C34H26O8 (562.1627596000001)


Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM[2]. Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM[2]. Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with IC50 of 3.99 μM[2].

   

3-(2,4-dihydroxyphenyl)-7-[(1z)-2-(2,4-dihydroxyphenyl)ethenyl]-13-methyl-4,14-dioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]henicosa-2,5,7,9,11,15,17,19-octaene-9,17-diol

3-(2,4-dihydroxyphenyl)-7-[(1z)-2-(2,4-dihydroxyphenyl)ethenyl]-13-methyl-4,14-dioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]henicosa-2,5,7,9,11,15,17,19-octaene-9,17-diol

C34H26O8 (562.1627596000001)


   

albanol a

Albanol A; BDBM50251015; CHEMBL454705; MJJWBJFYYRAYKU-WLKQUGLZSA-N

C34H26O8 (562.1627596000001)


{"Ingredient_id": "HBIN015062","Ingredient_name": "albanol a","Alias": "Albanol A; BDBM50251015; CHEMBL454705; MJJWBJFYYRAYKU-WLKQUGLZSA-N","Ingredient_formula": "C34H26O8","Ingredient_Smile": "CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C6=CC7=C(O6)C=C(C=C7)O)C8=C(C=C(C=C8)O)O","Ingredient_weight": "562.6 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "SMIT14219","TCMID_id": "846","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "44567218","DrugBank_id": "NA"}

   

(1s,9s,13r,21r)-1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

(1s,9s,13r,21r)-1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

C34H26O8 (562.1627596000001)


   

4-{2,3,5,6-tetrahydroxy-4'-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-4-yl}phenyl 2-phenylacetate

4-{2,3,5,6-tetrahydroxy-4'-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-4-yl}phenyl 2-phenylacetate

C34H26O8 (562.1627596000001)


   

3,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl 2-phenylacetate

3,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl 2-phenylacetate

C34H26O8 (562.1627596000001)


   

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl 2-phenylacetate

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl 2-phenylacetate

C34H26O8 (562.1627596000001)


   

2,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-[(3-phenylpropanoyl)oxy]-[1,1'-biphenyl]-3-yl benzoate

2,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-[(3-phenylpropanoyl)oxy]-[1,1'-biphenyl]-3-yl benzoate

C34H26O8 (562.1627596000001)


   

(9r)-1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

(9r)-1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

C34H26O8 (562.1627596000001)


   

(1s,13r,21s)-1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

(1s,13r,21s)-1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

C34H26O8 (562.1627596000001)


   

1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

C34H26O8 (562.1627596000001)


   

(1r,9s,13s,21r)-1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

(1r,9s,13s,21r)-1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-3,5,7,11,14,16,18-heptaene-5,15-diol

C34H26O8 (562.1627596000001)