pomolic acid (Q27135401)

Pomolic acid (English)

(1R,2S,4aS,6aR,6aS,6bS,8aS,10S,12aS,14bR)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

7 October 2016

stereoisomer of

2 references

(1R,2R,4aS,6aR,6aS,6bR,8aR,10R,12aR,14bS)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

2 references

(1R,2S,4aS,6aR,6aS,6bR,8aS,10S,12aR,14bR)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

2 references

(1R,2R,4aS,6aR,6aS,6bR,8aS,10S,12aR,14bS)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

chemical formula

C₃₀H₄₈O₄

1 reference

Pomolic acid (English)

18 November 2016

canonical SMILES

CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O

1 reference

Pomolic acid (English)

18 November 2016

isomeric SMILES

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

1 reference

Pomolic acid (English)

Mesosphaerum oblongifolium

18 November 2016

found in taxon

1 reference

Structure and stereochemistry of four α-pyrones from Hyptis oblongifolia

Rubus irenaeus

2 references

Chemical Constituents from the Peels of Citrus sudachi

Chemical constituents from the peels of Citrus sudachi

Couepia ulei

1 reference

Phenolic compounds obtained from stems of Couepia ulei with the potential to induce quinone reductase

Morinda citrifolia

1 reference

Anthraquinones with quinone reductase-inducing activity and benzophenones from Morinda citrifolia (noni) roots.

Sanguisorba officinalis

4 references

Pomolic acid derivatives from the root of Sanguisorba officinalis

Triterpene glycosides from the roots of Sanguisorba officinalis

Triterpene glycosides from the roots of Sanguisorba officinalis

Triterpene glycosides from the roots of Sanguisorba officinalis

Diospyros kaki

3 references

Effect of five triterpenoid compounds isolated from leaves of Diospyros kaki on stimulus-induced superoxide generation and tyrosyl phosphorylation in human polymorphonuclear leukocytes

Triterpenoids from the leaves of Diospyros kaki (persimmon) and their inhibitory effects on protein tyrosine phosphatase 1B.

Three minor novel triterpenoids from the leaves of Diospyros kaki.

Agrimonia pilosa

1 reference

Phenolic Components from the Aerial Parts of Agrimonia pilosa

Scutellaria lateriflora

2 references

Scuteflorins A and B, dihydropyranocoumarins from Scutellaria lateriflora

Scuteflorins A and B, Dihydropyranocoumarins from Scutellaria lateriflora L.

Polylepis racemosa

1 reference

Cytotoxic triterpene acids from the Peruvian medicinal plant Polylepis racemosa

Cecropia pachystachya

1 reference

Anti-inflammatory and apoptotic activities of pomolic acid isolated from Cecropia pachystachya.

Lantana camara

2 references

Pentacyclic triterpenoids from Lantana camara

Constituents from the Root of Lantana camara

Markhamia tomentosa

1 reference

Antiprotozoal activities of some constituents of Markhamia tomentosa (Bignoniaceae).

Olea europaea

2 references

Production of triterpene acids by cell suspension cultures of Olea europaea

Production of triterpene acids by cell suspension cultures of Olea europaea

Lantana montevidensis

1 reference

New pentacyclic triterpenoid from the roots of Lantana montevidensis (spreng.) briq. cultivated in Egypt

Acaena pinnatifida

1 reference

Triterpenoids from Acaena pinnatifida R. et P.

Chaenomeles japonica

3 references

A new acylated triterpene from the roots of Chaenomeles japonica

A New Acylated Triterpene from the Roots of Chaenomeles japonica.

A new acylated triterpene from the roots of Chaenomeles japonica

Chaenomeles speciosa

1 reference

Inhibition of PGHS-1 and PGHS-2 by Triterpenoid Acids from Chaenomelis Fructus

Chrysobalanus icaco

2 references

Pentacyclic triterpenes from Chrysobalanaceae species: cytotoxicity on multidrug resistant and sensitive leukemia cell lines

Phytochemical study and antimicrobial activity of Chrysobalanus icaco

Cowania mexicana

1 reference

Triterpene Acids from Cowainea mexicana

Purshia mexicana

1 reference

Triterpene Acids from Cowainea mexicana

Debregeasia salicifolia

1 reference

Antimicrobial triterpenes from Debregeasia salicifolia

Desfontainia fulgens

1 reference

Triterpenoids from Desfontainia spinosa

Desfontainia spinosa

1 reference

Triterpenoids from Desfontainia spinosa

Diospyros melanoxylon

2 references

Triterpene acids from Diospyros melanoxylon

Diospyros melanoxylon Leaves: A Rich Source of Pentacyclic Triterpenes

Mandevilla martiana

1 reference

Proposed active constituents of Dipladenia martiana

Freziera

1 reference

Pentacyclic triterpenoids from Freziera sp. that inhibit DNA polymerase beta

Moquilea licaniaeflora

1 reference

Triterpenes from Licania licaniaeflora.

Musanga cecropioides

2 references

Cecropioic acid, a pentacyclic triterpene from Musanga cecropioides

Further Triterpenoids of Musanga cecropioides: The Structure of Cecropic Acid

Myrianthus serratus

1 reference

An E-ring γ-lactone pentacyclic triterpene from Myrianthus serratus

Nauclea orientalis

1 reference

Isolation, Partial Synthesis and Stereochemical Study of 10-Hydroxystrictosamide, a Constituent of Nauclea orientalis in Thailand

basil

1 reference

Basil (Ocimum basilicum L.)

Picramnia sellowii

1 reference

Triterpenes and anthraquinones from Picramnia sellowii Planchon in Hook (Simaroubaceae)

Rosa bella

1 reference

Chemical Constituents from Fruit of

Rosa davurica

2 references

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

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

Complex-toothed flying squirrel

1 reference

Cytotoxic triterpenes from a Chinese medicine, Goreishi

Euscaphis japonica

3 references

Cytotoxic Hexacyclic Triterpene Acids from Euscaphis japonica

Studies on constituents of medicinal plants. XIII. Constituents of the pericarps of the capsules of Euscaphis japonica Pax

Cytotoxic Hexacyclic Triterpene Acids from Euscaphis japonica

Weigela subsessilis

1 reference

Anti-complementary Activity of Ursane-Type Triterpenoids from Weigela subsessilis

Anaphalis margaritacea

1 reference

Flavonoids and triterpenoids from Anaphalis margaritacea

Anaphalis sinica

1 reference

Chemical Components ofAnaphalis SinicaHance

Fridericia triplinervia

1 reference

Trypanocidal activity of triterpenes from Arrabidaea triplinervia and derivatives

Berberis koreana

1 reference

Bioactivity-guided isolation of cytotoxic triterpenoids from the trunk of Berberis koreana

Callicarpa pentandra

1 reference

Four new clerodane diterpenoids from Callicarpa pentandra

Centella asiatica

1 reference

Antiproliferative constituents from Umbelliferae plants VII. Active triterpenes and rosmarinic acid from Centella asiatica

Coussarea macrophylla

1 reference

New anthracene derivatives from Coussarea macrophylla.

Cyclolepis genistoides

1 reference

Triterpenes and sesquiterpene lactones from Cyclolepis genistoides

Cydonia oblonga

1 reference

Antioxidant and antiproliferative activities of phytochemicals from Quince (Cydonia vulgaris) peels

Cydonia vulgaris

1 reference

Antioxidant and antiproliferative activities of phytochemicals from Quince (Cydonia vulgaris) peels

Strobilanthes psilostachys

1 reference

Novel cadinane and norcadinane sesquiterpenes and a new propanoate from Goldfussia psilostachys

Hippophae rhamnoides

1 reference

Chemical constituents from the fruits of Hippophae rhamnoides

Isodon scoparius

1 reference

ent-Clerodanoids fromIsodon scoparius

Oreocnide frutescens

1 reference

A new natural azulene-type pigment from Oreocnide frutescens

Perilla frutescens

1 reference

Triterpene acids from the leaves of Perilla frutescens and their anti-inflammatory and antitumor-promoting effects

Planchonella duclitan

1 reference

Triterpene Acids from the Leaves ofPlanchonella Duclitan(Blanco) Bakhuizan

Stereospermum acuminatissimum

1 reference

Phenol esters and other constituents from the stem barks of Stereospermum acuminatissimum

Strobilanthes dimorphotricha

1 reference

Novel cadinane and norcadinane sesquiterpenes and a new propanoate from Goldfussia psilostachys

Strobilanthes pentstemonoides

1 reference

Novel cadinane and norcadinane sesquiterpenes and a new propanoate from Goldfussia psilostachys

Perilla frutescens var. frutescens

1 reference

Cytotoxic activity of Perilla frutescens var. japonica leaf extract is due to high concentrations of oleanolic and ursolic acids

Rhaponticum uniflorum

1 reference

Triterpenoids fromRhaponticum Uniflorum

Leucosceptrum

1 reference

[Studies on the constituents of Leucoseptrum stellipillum]

Salvia officinalis

1 reference

Bestandteile von Salvia officinalis

Debregeasia saeneb

1 reference

Antimicrobial triterpenes from Debregeasia salicifolia

Comanthosphace stellipila

1 reference

[Studies on the constituents of Leucoseptrum stellipillum]

Pimpinella saxifraga

1 reference

Chemical Constituents of the Genus Pimpinella

Pimpinella major

1 reference

Chemical Constituents of the Genus Pimpinella

Identifiers

InChI

InChI=1S/C30H48O4/c1-18-10-15-30(24(32)33)17-16-27(5)19(23(30)29(18,7)34)8-9-21-26(4)13-12-22(31)25(2,3)20(26)11-14-28(21,27)6/h8,18,20-23,31,34H,9-17H2,1-7H3,(H,32,33)/t18-,20+,21-,22+,23-,26+,27-,28-,29-,30+/m1/s1

1 reference

Pomolic acid (English)

18 November 2016

2 references

Pomolic acid (English)

18 November 2016

ChEBI release 2020-09-01

CAS Registry Number

13849-91-7

2 references

Global Substance Registration System

UNII

60HAB1ZK1T

pomolic acid (English)

18 November 2016

https://commonchemistry.cas.org/detail?cas_rn=13849-91-7

9 April 2021

1 reference

(3beta)-3,19-Dihydroxyurs-12-en-28-oic acid (English)

18 November 2016

2 references

Pomolic acid (English)

18 November 2016

ChEBI ID

66772

mapping relation type

2 references

POMOLIC ACID (English)

18 November 2016

International Chemical Identifier

InChI

InChI=1S/C30H48O4/c1-18-10-15-30(24(32)33)17-16-27(5)19(23(30)29(18,7)34)8-9-21-26(4)13-12-22(31)25(2,3)20(26)11-14-28(21,27)6/h8,18,20-23,31,34H,9-17H2,1-7H3,(H,32,33)/t18-,20+,21-,22+,23-,26+,27-,28-,29-,30+/m1/s1

1 reference

POMOLIC ACID (English)

18 November 2016

2 references

1 reference

1 reference

DSSTOX compound identifier

0 references

2 references

Global Substance Registration System

UNII

60HAB1ZK1T

pomolic acid (English)

18 November 2016