(Q27109939)

inferred from SMILES

mass

448.35526±0 dalton

1 reference

Typhasterol (English)

(3R,5S,8S,9S,10R,13S,14R,17R)-17-[(2S,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-3-hydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one

5 October 2016

stereoisomer of

1 reference

(3S,5S,8S,9S,10R,13R,14S,17R)-17-[(2S,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-3-hydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one

1 reference

(3R,5S,8S,9S,10R,13R,14S,17R)-17-[(2S,3R,4R,5R)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-3-hydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one

1 reference

1 reference

(3R,5S,8S,9S,10R,13R,14S,17R)-17-[(2S,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-3-hydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one

1 reference

(3S,5S,8S,9S,10R,13S,14S,17R)-17-[(2R,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-3-hydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one

1 reference

(3S,5S,8S,9S,10R,13R,14S,17R)-17-[(2S,3R,4R,5R)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-3-hydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one

1 reference

chemical formula

C₂₈H₄₈O₄

1 reference

Typhasterol (English)

5 October 2016

canonical SMILES

CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(C4)O)C)C)O)O

1 reference

Typhasterol (English)

5 October 2016

isomeric SMILES

C[C@@H]([C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC(=O)[C@@H]4[C@@]3(CC[C@H](C4)O)C)C)[C@H]([C@@H]([C@@H](C)C(C)C)O)O

1 reference

Secasterone, the first naturally occurring 2,3-epoxybrassinosteroid from Secale cereale

Typhasterol (English)

5 October 2016

1 reference

Camellia sinensis

1 reference

A new brassinolide-related steroid in the leaves of Thea sinensis.

Senna tora

2 references

Brassinosteroids and Monoglycerides in Immature Seeds ofCassia toraas the Active Principles in the Rice Lamina Inclination Bioassay

Brassinosteroids and Monoglycerides in Immature Seeds ofCassia toraas the Active Principles in the Rice Lamina Inclination Bioassay

Catharanthus roseus

1 reference

Possible Involvement of 3-Dehydroteasterone in the Conversion of Teasterone to Typhasterol in Cultured Cells ofCatharanthus roseus

Cryptomeria japonica

2 references

Identification of Brassinosteroids with Epimerized Substituents and/or the 23-Oxo Group in Pollen and Anthers of Japanese Cedar

Cryptolide, a New Brassinolide Catabolite with a 23-oxo group from Japanese cedar pollen/anther and its synthesis

Distylium racemosum

1 reference

3-Oxoteasterone and the Epimerization of Teasterone: Identification in Lily Anthers andDistylium racemosumLeaves and Its Biotransformation into Typhasterol

Lilium elegans

1 reference

Identification of Brassinolide, Castasterone, Typhasterol, and Teasterone from the Pollen ofLilium elegans

Lilium longiflorum

1 reference

3-Oxoteasterone and the Epimerization of Teasterone: Identification in Lily Anthers andDistylium racemosumLeaves and Its Biotransformation into Typhasterol

Marchantia polymorpha

1 reference

In Vivo and in Vitro Conversion of Teasterone to Typhasterol in Cultured Cells of Marchantia polymorpha

Picea sitchensis

1 reference

Steroidal plant growth regulators, castasterone and typhasterol (2-deoxycastasterone) from the shoots of sitka spruce (Picea sitchensis)

Pinus thunbergii

1 reference

2-Deoxycastasterone, a new brassinolide-related bioactive steroid from Pinus pollen.

Robinia pseudoacacia

1 reference

Identification of Castasterone, 6-Deoxocastasterone, and Typhasterol in the Pollen ofRobinia pseudo-acaciaL.

Triticum aestivum

1 reference

3-Dehydroteasterone, a 3,6-Diketobrassinosteroid as a Possible Biosynthetic Intermediate of Brassinolide from Wheat Grain

Typha latifolia

2 references

Typhasterol (2-deoxycastasterone): a new plant growth regulator from cat-tail pollen

Typhasterol (2-deoxycastasterone): a new plant growth regulator from cat-tail pollen

maize

1 reference

Identification of castasterone, typhasterol and teasterone from the pollen of Zea mays.

Erythronium japonicum

1 reference

Free and Conjugated Brassinosteroids in the Pollen and Anthers ofErythronium japonicumDecne.

Brassica juncea

1 reference

Arsenic induced modulation of antioxidative defense system and brassinosteroids in Brassica juncea L

Oryza sativa

1 reference

Biosynthetic relationship between C₂₈-brassinosteroids and C₂₉-brassinosteroids in rice (Oryza sativa) seedlings

Identifiers

InChI

InChI=1S/C28H48O4/c1-15(2)16(3)25(31)26(32)17(4)20-7-8-21-19-14-24(30)23-13-18(29)9-11-28(23,6)22(19)10-12-27(20,21)5/h15-23,25-26,29,31-32H,7-14H2,1-6H3/t16-,17-,18+,19-,20+,21-,22-,23+,25+,26+,27+,28+/m0/s1

1 reference

Typhasterol (English)

5 October 2016

2 references

Typhasterol (English)

5 October 2016

ChEBI release 2020-09-01

2 references

typhasterol (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=87734-68-7

9 April 2021

1 reference

Typhasterol (English)

5 October 2016

2 references

Typhasterol (English)

5 October 2016

Reaxys registry number

3629989

1 reference

typhasterol (English)

5 October 2016

ChEBI ID

27173

mapping relation type

2 references

typhasterol (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C28H48O4/c1-15(2)16(3)25(31)26(32)17(4)20-7-8-21-19-14-24(30)23-13-18(29)9-11-28(23,6)22(19)10-12-27(20,21)5/h15-23,25-26,29,31-32H,7-14H2,1-6H3/t16-,17-,18+,19-,20+,21-,22-,23+,25+,26+,27+,28+/m0/s1

1 reference

1 reference

DSSTOX compound identifier

DTXCID3021146

0 references

Human Metabolome Database ID

HMDB0034423

2 references

inferred from InChIKey

1 reference

typhasterol (English)

5 October 2016

UNII

GG2V86UZ00

1 reference

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

typhasterol (English)

5 October 2016

1 reference