(Q105365308)

English

(1R,3aS,5aS,5bR,9R,10R,11aR)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysene-3a-carboxylic acid

group of stereoisomers with the chemical formula C₃₀H₄₆O₄

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instance of

group of stereoisomers

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1 reference

470.339609952 dalton

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based on heuristic

inferred from SMILES

chemical formula

C₃₀H₄₆O₄

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canonical SMILES

O=C(O)C12CCC(C(=C)C)C2C3=CCC4C5(C)CC(O)C(O)C(C)(C)C5CCC4(C)C3(C)CC1

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isomeric SMILES

C=C(C)[C@@H]1CC[C@]2(C(=O)O)CC[C@]3(C)C(=CCC4[C@@]5(C)C[C@@H](O)[C@H](O)C(C)(C)C5CC[C@]43C)C12

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found in taxon

Alphitonia excelsa

1 reference

stated in

Constituents of Alphitonia Species. III. Alphitexolide, a New Triterpene, and Other Extractives

Alphitonia petriei

2 references

stated in

Constituents of Alphitonia Species. III. Alphitexolide, a New Triterpene, and Other Extractives

stated in

Further Constituents of Alphitonia Species

Alphitonia whitei

2 references

stated in

Constituents of Alphitonia Species. III. Alphitexolide, a New Triterpene, and Other Extractives

stated in

Further Constituents of Alphitonia Species

Chaenomeles sinensis

2 references

stated in

Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 mouse epidermal cells

stated in

Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 mouse epidermal cells

Cochlospermum

1 reference

stated in

Antiplasmodial compounds from Cochlospermum tinctorium

Dryobalanops aromatica

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stated in

Constituents of dipterocarpaceae resins. Part I. Triterpene acids of Dryobalanops aromatica

Ziziphus cambodiana

1 reference

stated in

Ceanothane- and lupane-type triterpenes with antiplasmodial and antimycobacterial activities from Ziziphus cambodiana

Eucalyptus camaldulensis

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stated in

Isolation and Structural Elucidation of Acylated Pentacyclic Triterpenoids from the Leaves ofEucalyptus camaldulensisvar.obtusa

Licania heteromorpha

2 references

stated in

Antimicrobial triterpenoids from Licania heteromorpha

stated in

Flavonoids and triterpenoids from Licania heteromorpha (Chrysobalanaceae)

Myrica rubra

2 references

stated in

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

stated in

Constituents of Myrica rubra. III. Structures of two glycosides of myricanol.

Plumeria obtusa

2 references

stated in

Pentacyclic triterpenoids from the leaves of Plumeria obtusa

stated in

Pentacyclic triterpenoids from the leaves of Plumeria obtusa

Rosa woodsii

1 reference

stated in

Anti-AIDS agents. 30. Anti-HIV activity of oleanolic acid, pomolic acid, and structurally related triterpenoids

Ziziphus jujuba

1 reference

stated in

Studies on the constituents of Zizyphi fructus. II. Structure of new p-coumaroylates of maslinic acid.

Ziziphus mauritiana

1 reference

stated in

Cytotoxic triterpenoids from the fruits of Zizyphus jujuba

Breynia fruticosa

1 reference

stated in

Triterpene and sterol derivatives from the roots of Breynia fruticosa

Ziziphus jujuba var. spinosa

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stated in

Characterization of triterpenic acids in fruits of ziziphus species by HPLC-ELSD-MS.

Prunus dulcis

1 reference

stated in

Antiproliferative terpenoids from almond hulls (Prunus dulcis): identification and structure-activity relationships.

Morella rubra

2 references

stated in

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

stated in

Constituents of Myrica rubra. III. Structures of two glycosides of myricanol.

Syzygium sandwicense

1 reference

stated in

Constituents of Eugenia sandwicensis with potential cancer chemopreventive activity.

Prunus avium

1 reference

stated in

Antiproliferative terpenoids from almond hulls (Prunus dulcis): identification and structure-activity relationships.

Eucalyptus globulus

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stated in

Cypellocarpin C and other compounds from the fruits of Eucalyptus globulus Labill.

Identifiers

InChI

InChI=1S/C30H46O4/c1-17(2)18-10-13-30(25(33)34)15-14-28(6)19(23(18)30)8-9-22-27(5)16-20(31)24(32)26(3,4)21(27)11-12-29(22,28)7/h8,18,20-24,31-32H,1,9-16H2,2-7H3,(H,33,34)/t18-,20+,21?,22?,23?,24-,27-,28+,29+,30-/m0/s1

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InChIKey

YVFUWFRLVWFNLF-LAYMWGLGSA-N

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1 reference

17 September 2022

inferred from InChIKey

1 reference

(Q105365308)

(1R,3aS,5aS,5bR,9R,10R,11aR)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysene-3a-carboxylic acid

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Identifiers

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