(Q27138611)

ocotillone (English)

7 October 2016

2 references

(5R,8R,9S,10R,13R,14R,17S)-17-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

2 references

2 references

(5R,8R,9S,10R,13R,14R,17S)-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

2 references

(5R,8R,9R,10R,13S,14R,17R)-17-[(2S,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

1 reference

chemical formula

C₃₀H₅₀O₃

1 reference

ocotillone (English)

7 October 2016

CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C

1 reference

ocotillone (English)

7 October 2016

C[C@@]12CC[C@@H]([C@H]1CC[C@H]3[C@]2(CC[C@@H]4[C@@]3(CCC(=O)C4(C)C)C)C)[C@@]5(CC[C@@H](O5)C(C)(C)O)C

1 reference

Triterpenoids from the floral spikes of Betula platyphylla var. japonica and their reversing activity against multidrug-resistant cancer cells

ocotillone (English)

7 October 2016

1 reference

Dysoxylum malabaricum

1 reference

Triterpenoids from Dysoxylum malabaricum

Aglaia leucophylla

1 reference

Secotirucallane triterpenes from the stem bark of Aglaia leucophylla

Aglaia foveolata

1 reference

Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris.

Aglaia rubiginosa

3 references

Cytotoxic constituents of the twigs and leaves of Aglaia rubiginosa.

Cytotoxic constituents of the twigs and leaves of Aglaia rubiginosa.

Cytotoxic Constituents of the Twigs and Leaves of Aglaia rubiginosa

Dysoxylum cauliflorum

1 reference

A triterpenoid with a novel abeo-dammarane skeleton from Dysoxylum cauliflorum

Forsythia suspensa

1 reference

A new furofuran mono-lactone from Forsythia suspensa

Amphipterygium adstringens

2 references

Tirucallane-type triterpenes from Juliania adstringens

Tirucallane-type triterpenes from Juliania adstringens

Simarouba versicolor

1 reference

Chemical constituents of Simarouba versicolor

Cabralea canjerana

1 reference

Effect of triterpenoids and limonoids isolated from Cabralea canjerana and Carapa guianensis (Meliaceae) against Spodoptera frugiperda (J. E. Smith).

Aglaia abbreviata

1 reference

Triterpenoids from Aglaia abbreviata and their cytotoxic activities.

Ailanthus altissima

1 reference

Triterpenoids and Sterones from the Stem Bark of Ailanthus altissima

Betula platyphylla var. japonica

1 reference

Triterpenoids from the floral spikes of Betula platyphylla var. japonica and their reversing activity against multidrug-resistant cancer cells

Aglaia elaeagnoidea

1 reference

Triterpenoids from Aglaia abbreviata and their cytotoxic activities.

Identifiers

InChI

InChI=1S/C30H50O3/c1-25(2)21-12-17-29(7)22(27(21,5)15-13-23(25)31)10-9-19-20(11-16-28(19,29)6)30(8)18-14-24(33-30)26(3,4)32/h19-22,24,32H,9-18H2,1-8H3/t19-,20+,21+,22-,24-,27+,28-,29-,30+/m1/s1

1 reference

XSQYWMLMQVUWSF-KATWBKOUSA-N

ocotillone (English)

7 October 2016

2 references

ocotillone (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

19865-86-2

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

English

title

(24R)-25-Hydroxy-20,24-epoxydammaran-3-one (English)

7 October 2016

2 references

matched by identifier from

English

title

ocotillone (English)

retrieved

7 October 2016

InChIKey

XSQYWMLMQVUWSF-KATWBKOUSA-N

Reaxys registry number

5307536

1 reference

ocotillone (English)

7 October 2016

mapping relation type

2 references

matched by identifier from

English

title

ocotillone (English)

retrieved

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C30H50O3/c1-25(2)21-12-17-29(7)22(27(21,5)15-13-23(25)31)10-9-19-20(11-16-28(19,29)6)30(8)18-14-24(33-30)26(3,4)32/h19-22,24,32H,9-18H2,1-8H3/t19-,20+,21+,22-,24-,27+,28-,29-,30+/m1/s1

1 reference