Indexed keywords
15 HYDROXYDEHYDROABIETIC ACID;
18 HYDROXYPODOCARPEN 8(14) EN 13 ONE;
18 SUCCINYLOXYABIETA 8,11,13 TRIENE METHYL ESTER;
7 OXODEHYDROABIETINOL;
8(14) PODOCARPEN 13 ON 18 OIC ACID;
8,11,13 ABIETATRIENE 15,18 DIOL;
8,11,13 ABIETATRIENE 7ALPHA, 18 DIOL;
ABIETA 7,17 DIENE 12ALPHA METHOXY 18 OIC ACID;
ABIFADINE A;
ABIFADINE B;
ABIFADINE C;
ABIFADINE D;
ABIFADINE E;
DITERPENOID;
ME 7 OXO 8,11,13 ABIETATRIENE 18 YL SUCCINATE;
METHYL 8,11,13 ABIETATRIENE 7ALPHA HYDROXYL 18 SUCCINATE;
TORREFEROL;
UNCLASSIFIED DRUG;
ABIETANE DERIVATIVE;
ANTIINFECTIVE AGENT;
ANTINEOPLASTIC AGENT;
ABIES;
ABIES FARGESII;
ANIMAL CELL;
ANTIBACTERIAL ACTIVITY;
ANTIFUNGAL ACTIVITY;
ANTIPROLIFERATIVE ACTIVITY;
ARTICLE;
B16 CELL LINE;
CANCER CELL LINE;
CANDIDA ALBICANS;
CARBON NUCLEAR MAGNETIC RESONANCE;
COLUMN CHROMATOGRAPHY;
CONTROLLED STUDY;
CRYSTAL STRUCTURE;
CYTOTOXICITY;
ESCHERICHIA COLI;
HEPG2 CELL LINE;
HETERONUCLEAR MULTIPLE BOND CORRELATION;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HUMAN;
HUMAN CELL;
IC50;
IN VITRO STUDY;
MCF 7 CELL LINE;
MOUSE;
NONHUMAN;
NUCLEAR OVERHAUSER EFFECT;
PLANT LEAF;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
SILICA GEL COLUMN CHROMATOGRAPHY;
SINGLE CRYSTAL X RAY DIFFRACTION;
STAPHYLOCOCCUS AUREUS;
STEREOCHEMISTRY;
X RAY DIFFRACTION;
ANIMAL;
CHEMICAL STRUCTURE;
CHEMISTRY;
CHINA;
DRUG EFFECTS;
ISOLATION AND PURIFICATION;
MICROBIAL SENSITIVITY TEST;
TUMOR CELL LINE;
X RAY CRYSTALLOGRAPHY;
ABIES;
ANIMALS;
ANTI-INFECTIVE AGENTS;
ANTINEOPLASTIC AGENTS, PHYTOGENIC;
CANDIDA ALBICANS;
CELL LINE, TUMOR;
CHINA;
CRYSTALLOGRAPHY, X-RAY;
DITERPENES, ABIETANE;
ESCHERICHIA COLI;
HUMANS;
INHIBITORY CONCENTRATION 50;
MICE;
MICROBIAL SENSITIVITY TESTS;
MOLECULAR STRUCTURE;
PLANT LEAVES;
STAPHYLOCOCCUS AUREUS;
1
84961179022
Science Press Beijing
W.J. Zhang, and L.G. Fu Flora of China 7 vols. 1978 Science Press Beijing 55 95
(1978)
Flora of China
, vol.7
, pp. 55-95
Zhang, W.J.1
Fu, L.G.2
3
41549139094
Abiesanordines A-N: Fourteen new norditerpenes from Abies georgei
X. Yang, S. Li, L. Feng, Y. Shen, J. Tian, X. Liu, H. Zeng, C. Zhang, and W. Zhang Abiesanordines A-N: fourteen new norditerpenes from Abies georgei Tetrahedron 64 2008 4354 4362
(2008)
Tetrahedron
, vol.64
, pp. 4354-4362
Yang, X.1
Li, S.2
Feng, L.3
Shen, Y.4
Tian, J.5
Liu, X.6
Zeng, H.7
Zhang, C.8
Zhang, W.9
4
76449087752
Isolation, structure, and bioactivities of abiesadines A-Y, 25 new diterpenes from Abies georgei Orr
X.W. Yang, L. Feng, S.M. Li, X.H. Liu, Y.L. Li, L. Wu, Y.H. Shen, J.M. Tian, X. Zhang, X.R. Liu, N. Wang, Y. Liu, and W.D. Zhang Isolation, structure, and bioactivities of abiesadines A-Y, 25 new diterpenes from Abies georgei Orr Bioorg. Med. Chem. 18 2010 744 754
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 744-754
Yang, X.W.1
Feng, L.2
Li, S.M.3
Liu, X.H.4
Li, Y.L.5
Wu, L.6
Shen, Y.H.7
Tian, J.M.8
Zhang, X.9
Liu, X.R.10
Wang, N.11
Liu, Y.12
Zhang, W.D.13
5
84880891879
Lanostane- and cycloartane-type triterpenoids from Abies balsamea oleoresin
S. Lavoie, C. Gauthier, J. Legault, S. Mercier, V. Mshvildadze, and A. Pichette Lanostane- and cycloartane-type triterpenoids from Abies balsamea oleoresin Beilstein J. Org. Chem. 9 2013 1333 1339
(2013)
Beilstein J. Org. Chem.
, vol.9
, pp. 1333-1339
Lavoie, S.1
Gauthier, C.2
Legault, J.3
Mercier, S.4
Mshvildadze, V.5
Pichette, A.6
6
67650258709
Terpenoid constituents of Abies chensiensis with potential anti-inflammatory activity
Y.L. Li, X.W. Yang, S.M. Li, Y.H. Shen, H.W. Zeng, X.H. Liu, J. Tang, and W.D. Zhang Terpenoid constituents of Abies chensiensis with potential anti-inflammatory activity J. Nat. Prod. 72 2009 1065 1068
(2009)
J. Nat. Prod.
, vol.72
, pp. 1065-1068
Li, Y.L.1
Yang, X.W.2
Li, S.M.3
Shen, Y.H.4
Zeng, H.W.5
Liu, X.H.6
Tang, J.7
Zhang, W.D.8
7
84867062091
New monoterpenes, diterpenes, and lignans from Abies recurvata
Y.L. Li, J.G. Zhang, P. Yu, B.L. Ke, J. Ye, X.W. Yang, H.Z. Jin, and W.D. Zhang New monoterpenes, diterpenes, and lignans from Abies recurvata Planta Med. 78 2012 1574 1578
(2012)
Planta Med.
, vol.78
, pp. 1574-1578
Li, Y.L.1
Zhang, J.G.2
Yu, P.3
Ke, B.L.4
Ye, J.5
Yang, X.W.6
Jin, H.Z.7
Zhang, W.D.8
9
84940650648
Bisabolane-type sesquiterpenoids from the whole plant of Parasenecio rubescens
A. Jin, W.M. Wu, H.Y. Yu, M. Zhou, Y. Liu, T. Tian, and H.L. Ruan Bisabolane-type sesquiterpenoids from the whole plant of Parasenecio rubescens J. Nat. Prod. 78 2015 2057 2066
(2015)
J. Nat. Prod.
, vol.78
, pp. 2057-2066
Jin, A.1
Wu, W.M.2
Yu, H.Y.3
Zhou, M.4
Liu, Y.5
Tian, T.6
Ruan, H.L.7
10
0000885037
New neutral diterpenes from southern pine tall oil
A.H. Conner, and J.W. Rowe New neutral diterpenes from southern pine tall oil Phytochemistry 16 1977 1777 1781
(1977)
Phytochemistry
, vol.16
, pp. 1777-1781
Conner, A.H.1
Rowe, J.W.2
11
84989056631
13C NMR data for abieta-8,11,13-triene diterpenoids
13C NMR data for abieta-8,11,13-triene diterpenoids Magn. Reson. Chem. 32 1994 774 781
(1994)
Magn. Reson. Chem.
, vol.32
, pp. 774-781
Miguel Del Corral, J.M.1
Gordaliza, M.2
Salinero, M.A.3
San Feliciano, A.4
12
0000896167
Abietane diterpenoids from Salvia pomifera
A. Ulubelen, and G. Topcu Abietane diterpenoids from Salvia pomifera Phytochemistry 31 1992 3949 3951
(1992)
Phytochemistry
, vol.31
, pp. 3949-3951
Ulubelen, A.1
Topcu, G.2
13
0021283258
The chemical composition of Baltic amber
J.S. Mills, R. White, and L.J. Gough The chemical composition of Baltic amber Chem. Geol. 47 1984 15 39
(1984)
Chem. Geol.
, vol.47
, pp. 15-39
Mills, J.S.1
White, R.2
Gough, L.J.3
14
84979458983
Diterpenoids in Pinus densiflora pollen
T. Shibuya Diterpenoids in Pinus densiflora pollen Sci. Rep. Hirosaki Univ. 38 1991 24 30
(1991)
Sci. Rep. Hirosaki Univ.
, vol.38
, pp. 24-30
Shibuya, T.1
16
78649817534
Systematicphytochemical investigation of Abies spectabilis
L. Wu, Y.L. Li, S.M. Li, X.W. Yang, J.H. Xia, L. Zhou, and W.D. Zhang Systematicphytochemical investigation of Abies spectabilis Chem. Pharm. Bull. 58 2010 1646 1649
(2010)
Chem. Pharm. Bull.
, vol.58
, pp. 1646-1649
Wu, L.1
Li, Y.L.2
Li, S.M.3
Yang, X.W.4
Xia, J.H.5
Zhou, L.6
Zhang, W.D.7