Plant Summary


  Plant Information

TCMBank_ID:

TCMBANKHE004985

ID:

TCMBANKHE004985

植物拉丁名:

Pteridium aquilinum var. latiusculum
显示图片

功能与主治:

To clear heat and disinhibit damp, downbear qi and transform phlegm, stanch bleeding./Common cold with fever, jaundice, dysentery, vaginal discharge, dysphagia-occlusion, tuberculosis and hemoptysis, intestinal wind bleeding, wind-damp impediment pain.

药用植物名:


药用部位:

tender leaf

TCM_ID_id:

3907


   植物对应的化合物
化合物ID 化合物名 别名 分子式 分子质量 Smiles
TCMBANKIN002529 pteroside a AC1L54AR; 35910-15-7; Pteroside A; (S)-6-(2-(beta-D-Glucopyranosyloxy)ethyl)-2,3-dihydro-3-hydroxy-2,5,7-trimethyl-1H-inden-1-one; (2S)-2-(hydroxymethyl)-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-3H-inden-1-one; 1H-Inden-1-one, 6-(2-(beta-D-glucopyranosyloxy)ethyl)-2,3-dihydro-3-hydroxy-2,5,7-trimethyl-, (S)- C21H30O8 410.5 g/mol CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)CO
TCMBANKIN002734 poncirin C28H34O14 594.56 CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)OC)O)CO)O)O)O)O)O
TCMBANKIN003829 Pterosin F pterosin f C14H17ClO 236.73 g/mol CC1CC2=C(C1=O)C(=C(C(=C2)C)CCCl)C
TCMBANKIN009530 ponasteroside a C33H54O11 626.8 g/mol CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC5C(C(C(C(O5)CO)O)O)O)O)C)C)O)O)O
TCMBANKIN017379 palustric acid palustricacid C20H30O2 302.5 g/mol CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C
TCMBANKIN019839 pterosin k C15H19ClO2 266.76 g/mol CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2)(C)CO
TCMBANKIN020980 acetylpterosin c C16H20O4 276.33 g/mol CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC(=O)C)C)O
TCMBANKIN021472 pteroside c C20H28O8 396.4 g/mol CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O
TCMBANKIN021714 pterosin g C14H18O3 234.29 g/mol CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)CO
TCMBANKIN022433 pterosin c C14H18O3 234.29 g/mol CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O
TCMBANKIN022711 pterosin j C14H17ClO2 252.73 g/mol CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCCl)C)O
TCMBANKIN024049 pteroside d C21H30O8 410.5 g/mol CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2O)(C)C
TCMBANKIN024571 benzoylpterosin b C21H22O3 CC1CC2=CC(=C(C(=C2C1=O)C)CCOC(=O)C3=CC=CC=C3)C
TCMBANKIN024834 pteroside z C21H30O7 394.5 g/mol CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)C
TCMBANKIN028035 pterolactam C5H9NO2 115.13 g/mol COC1CCC(=O)N1
TCMBANKIN030755 pterosin l C15H20O4 264.32 g/mol CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)CO
TCMBANKIN031257 pterosterone C27H44O7 480.6 g/mol CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O
TCMBANKIN031802 pterosin a C15H20O3 248.32 g/mol CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)CO
TCMBANKIN032718 pterosin z C15H20O2 232.32 g/mol CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)C
TCMBANKIN033176 ponasterone a C27H44O6 464.6 g/mol CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O
TCMBANKIN033608 pterosin d C15H20O3 248.32 g/mol CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)C
TCMBANKIN035621 pterosin e C14H16O3 232.27 g/mol CC1CC2=C(C1=O)C(=C(C(=C2)C)CC(=O)O)C
TCMBANKIN036797 Pterostilbene 4-[2-(3,5-dimethoxyphenyl)vinyl]phenol; 3,5-dimethoxy-4'-hydroxystilbene; 4-[(E)-2-(3,5-dimethoxyphenyl)ethenyl]phenol; Phenol, 4-(2-(3,5-dimethoxyphenyl)ethenyl)-, (E)-; trans-3,5-Dimethoxy-4&prime;-hydroxystilbene; C10287; 3,5-Dimethoxy-4'-hydroxy-trans-stilbene; Pterocarpus marsupium; 537-42-8; Pterostilbene, <i>Pterocarpus marsupium; pterostilbene ; ACon1_000305; 4-[2-(3,5-dimethoxyphenyl)ethenyl]phenol; 4-[(E)-2-(3,5-dimethoxyphenyl)vinyl]phenol; MLS000863581; 3',5'-Dimethoxy-4-stilbenol; 4-[(1E)-2-(3,5-Dimethoxyphenyl)ethenyl]phenol; MEGxp0_000345; NSC613735; 4-(2-(3,5-Dimethoxyphenyl)ethenyl)phenol; SMR000440694; 3,5-Dimethoxy-4&#8242;-hydroxystilbene; P1499_SIGMA; MLS000759434; pterostilbene; 4-Stilbenol, 3',5'-dimethoxy-, (E)- C16H16O3 256.3 COC1=CC(=CC(=C1)C=CC2=CC=C(C=C2)O)OC
TCMBANKIN037119 pterosin n C14H18O3 234.29 g/mol CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)O
TCMBANKIN038916 (2S)-Pteroside K
TCMBANKIN040417 Ptaquiloside 398.45
TCMBANKIN041991 Isocryptomerin 6-[4-(5,7-dihydroxy-4-keto-chromen-2-yl)phenoxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-chromone; CHEMBL3589108; 6-[4-(5,7-dihydroxy-4-oxo-chromen-2-yl)phenoxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-chromen-4-one; 6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)phenoxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one; isocryptomerin; 20931-58-2; 6-[4-(5,7-Dihydroxy-4-oxo-4H-chromen-2-yl)phenoxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-chromen-4-one; 6-[4-(5,7-dihydroxy-4-oxo-2-chromenyl)phenoxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-chromenone; SCHEMBL13485651; AC1NSWZB; Isocyptomerin; isocryptomerin C31H20O10 552.48 COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O
TCMBANKIN047008 Isocrotonoylpterosin B
TCMBANKIN048597 palmitoylpterosin a C31H50O4 CCCCCCCCCCCCCCCC(=O)OCCC1=C(C=C2CC(C(=O)C2=C1C)(C)CO)C
TCMBANKIN050075 (2s,3r)-pteroside c C20H28O8 CC1C(C2=CC(=C(C(=C2C1=O)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O
TCMBANKIN058379 indican AoEassAssa(1/4)ONI; Indoxyl sulfate potassium salt; AC33706; 487-94-5 (Parent); Sulfuric acid= (1H-indol-3-yl)=potassium ester salt; TRA0056760; SMR000875350; 3-Indoxylsulfuric acid, potassium salt; Potassium indoxyl sulfate; CCG-53133; 2642-37-7; AX8087438; AK-81568; ACM2642377; KS-000018CM; 3-Indoxyl sulfate, potassium salt; SR-01000642319-1; 567HMW942W; MFCD00037931; MolPort-000-141-472; SBB100973; ST24048980; 2355AB; LS-83683; 3-Indoxyl sulfate potassium salt; 3-Indolyl sulphate potassium salt; potassium ion indol-3-yl sulfate; AKOS024306954; Indol-3-ol, potassium sulfate; ANW-58467; DTXSID70181012; 3-hydroxyindol; I14-91729; TC-147212; AKOS016003133; Indol-3-yl sulfate, potassium salt; 1309597-66-7; Indol-3-yl potassium sulfate; Urinary indican; 4CH-021488; SCHEMBL10550536; C8H6KNO4S; indol-3-yl hydroxysulfonate, potassium salt; Indican (urinary); AC1NPD4O; 3-oC>>ussAssaAoEa(1/4)O; 1H-INDOL-3-YL POTASSIUM SULFATE; 1H-Indol-3-ol,3-(hydrogen sulfate), potassium salt (1:1); MLS001361369; 39026A; UNII-567HMW942W; EINECS 220-145-5; Potassium indol-3-yl sulphate; CTK8B7765; FT-0615879; potassium 1H-indol-3-yl sulfate; ST50307657; INDOL-3-OL, HYDROGEN SULFATE (ester), POTASSIUM SALT; CHEMBL1452061; Potassium indol-3-yl sulfate; I-6350; MDAWATNFDJIBBD-UHFFFAOYSA-M;ZINC04097614; (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(1H-indol-3-yloxy)oxane-3,4,5-triol; SMP2_000304; 487-60-5; Indican glucoside; (2S,3R,4S,5S,6R)-2-(1H-indol-3-yloxy)-6-methylol-tetrahydropyran-3,4,5-triol; C08481; 1328-73-0; (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(1H-indol-3-yloxy)tetrahydropyran-3,4,5-triol;Indican, plant C14H17NO6 295.29g/mol C1=CC=C2C(=C1)C(=CN2)OC3C(C(C(C(O3)CO)O)O)O
TCMBANKIN058575 1-indanone 2,3-dihydro-1H-inden-1-one C9H8O 132.16 g/mol C1CC(=O)C2=CC=CC=C21
TCMBANKIN060414 (2R)-6-(2-hydroxyethyl)-2,5,7-trimethyl-1-indanone C14H18O2 218.29 CC1CC2=C(C1=O)C(=C(C(=C2)C)CCO)C
TCMBANKIN060415 pterosin C 3- O- β- D- glucosidede C20H28O7 CC1CC2=CC(=C(C(=C2C1=O)C)CCOC3C(C(C(C(O3)CO)O)O)O)C
TCMBANKIN061076 palmitoylpterosin c C30H48O4 CCCCCCCCCCCCCCCC(=O)OCCC1=C(C=C2C(C(C(=O)C2=C1C)C)O)C
TCMBANKIN061077 palmitoylpterosin b C30H48O3 CCCCCCCCCCCCCCCC(=O)OCCC1=C(C=C2CC(C(=O)C2=C1C)C)C

   植物对应的疾病
疾病ID 病名 疾病类型 MeSH 参考文献

   植物对应的靶点
靶点ID 基因名 基因别名 描述 染色体位置 Map_Location 基因类型