(Q27136070)

Alphitolic acid (English)

(1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aR,13bS)-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,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid

7 October 2016

stereoisomer of

1 reference

(1R,3aR,5aR,5bR,7aS,9R,10R,11aR,11bS,13aS,13bR)-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,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid

inferred from InChIKey

2 references

inferred from InChIKey

2alpha,3alpha-Dihydroxylupa-20(29)-ene-28-oic acid

inferred from InChI

1 reference

(1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aS,13bS)-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,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₃₀H₄₈O₄

1 reference

Alphitolic acid (English)

7 October 2016

canonical SMILES

CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)O

1 reference

Alphitolic acid (English)

7 October 2016

isomeric SMILES

CC(=C)[C@@H]1CC[C@]2([C@H]1[C@H]3CC[C@H]4[C@]([C@@]3(CC2)C)(CC[C@@H]5[C@@]4(C[C@H]([C@@H](C5(C)C)O)O)C)C)C(=O)O

1 reference

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

Alphitolic acid (English)

7 October 2016

2 references

Triterpenoid acids from Ziziphus jujuba

Myrica rubra

2 references

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

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

Plumeria obtusa

2 references

Pentacyclic triterpenoids from the leaves of Plumeria obtusa

Pentacyclic triterpenoids from the leaves of Plumeria obtusa

Alphitonia petriei

1 reference

Further Constituents of Alphitonia Species

Alphitonia whitei

1 reference

Further Constituents of Alphitonia Species

Chaenomeles sinensis

2 references

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

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

Eucalyptus camaldulensis

1 reference

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

Licania heteromorpha

3 references

Flavonoids and triterpenoids from Licania heteromorpha (Chrysobalanaceae)

Antimicrobial triterpenoids from Licania heteromorpha

Antimicrobial triterpenoids from Licania heteromorpha

basil

1 reference

Basil (Ocimum basilicum L.)

Rosa davurica

1 reference

Chemical constituents of pericarps of Rosa davurica Pall., a traditional Chinese medicine

Rosa woodsii

1 reference

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

Breynia fruticosa

1 reference

Triterpene and sterol derivatives from the roots of Breynia fruticosa

Akebia trifoliata

1 reference

Triterpenes and triterpene saponins from the stems of Akebia trifoliata.

Cochlospermum tinctorium

1 reference

Antiplasmodial compounds from Cochlospermum tinctorium

Gouania ulmifolia

1 reference

Triterpenoids from Gouania ulmifolia

Prunus dulcis

1 reference

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

Quercus aliena

1 reference

Three New 24-Noroleanane Triterpenoids fromQuercus aliena var.acuteserrata

Ugni molinae

1 reference

Topical anti-inflammatory activity of 2alpha-hydroxy pentacyclic triterpene acids from the leaves of Ugni molinae

Ziziphus jujuba var. spinosa

1 reference

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

Ziziphus mauritiana

1 reference

Cytotoxic triterpenoids from the fruits of Zizyphus jujuba

Streptomyces pristinaespiralis

1 reference

Improvement of pristinamycin I (PI) production in Streptomyces pristinaespiralis by metabolic engineering approaches.

Morella rubra

2 references

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

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

Syzygium sandwicense

1 reference

Constituents of Eugenia sandwicensis with potential cancer chemopreventive activity.

Prunus avium

1 reference

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

Identifiers

InChI

InChI=1S/C30H48O4/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/h18-24,31-32H,1,8-16H2,2-7H3,(H,33,34)/t18-,19+,20+,21-,22+,23+,24-,27-,28+,29+,30-/m0/s1

1 reference

Alphitolic acid (English)

PFCVZKFJHRCLCC-PGOIBATFSA-N

7 October 2016

InChIKey

2 references

Alphitolic acid (English)

7 October 2016

ChEBI release 2020-09-01

2 references

2alpha,3beta-dihydroxy-20(29)-lupen-28-oic acid (English)

PFCVZKFJHRCLCC-PGOIBATFSA-N

7 October 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=19533-92-7

1 reference

(2alpha,3beta)-2,3-Dihydroxylup-20(29)-en-28-oic acid (English)

7 October 2016

1 reference

Alphitolic acid (English)

7 October 2016

Reaxys registry number

5648545

1 reference

2alpha,3beta-dihydroxy-20(29)-lupen-28-oic acid (English)

7 October 2016

ChEBI ID

67600

mapping relation type

1 reference

2alpha,3beta-dihydroxy-20(29)-lupen-28-oic acid (English)

7 October 2016

1 reference

DSSTOX compound identifier

ALPHITOLIC ACID (English)

7 October 2016

1 reference

0 references

0 references

1 reference

2alpha,3beta-dihydroxy-20(29)-lupen-28-oic acid (English)