(Q1907191)

Maslinic acid (English)

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

7 October 2016

stereoisomer of

1 reference

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

2 references

2 references

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

1 reference

1 reference

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

inferred from InChI

1 reference

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

inferred from InChI

1 reference

1 reference

C₃₀H₄₈O₄

1 reference

Maslinic acid (English)

7 October 2016

canonical SMILES

CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C

1 reference

Maslinic acid (English)

7 October 2016

isomeric SMILES

C[C@@]12CC[C@@H]3[C@@]([C@H]1CC=C4[C@]2(CC[C@@]5([C@H]4CC(CC5)(C)C)C(=O)O)C)(C[C@H]([C@@H](C3(C)C)O)O)C

1 reference

Pentacyclic triterpenoids from Prunella vulgaris

Maslinic acid (English)

7 October 2016

3 references

Triterpenoids from Prunella vulgaris

Triterpenoic acids of Prunella vulgaris var. lilacina and their cytotoxic activities in vitro

Geum japonicum

6 references

The anticoagulant effects ofGeum japonicum extract and its constituents

Triterpenoids and glycosides from Geum japonicum

Anti-HIV triterpene acids from Geum japonicum

Terpenoids of Cultivated Salvia canariensis

Anti-HIV triterpene acids from Geum japonicum

Triterpenoids and glycosides from Geum japonicum

Salvia grandiflora

1 reference

Triterpene acids from Salvia and Teucrium species

Lamiaceae

2 references

Anti-inflammatory effects of maslinic acid, a natural triterpene, in cultured cortical astrocytes via suppression of nuclear factor-kappa B.

A novel antimicrobial abietane-type diterpene from Salvia albocaerulea.

Lavandula multifida

2 references

Extracts and constituents of Lavandula multifida with topical anti-inflammatory activity.

Extracts and constituents of Lavandula multifida with topical anti-inflammatory activity.

Akebia trifoliata

3 references

Triterpenes and triterpene saponins from the stems of Akebia trifoliata.

Triterpenes and Triterpene Saponins from the Stems of Akebia trifoliata.

Triterpenes and triterpene saponins from the stems of Akebia trifoliata.

Anisomeles indica

1 reference

Bioactive cembrane diterpenoids of Anisomeles indica

Baccharis linearis

1 reference

Diterpenoids from Baccharis linearis

Bidens subalternans

1 reference

Chemical components and anti-inflammatory activity from Bidens subalternans

Byrsonima crassifolia

2 references

Glycolipids from Byrsonima crassifolia

Glycolipids from Byrsonima crassifolia

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

Cornus capitata

1 reference

Constituents of Cornus capitata

Diospyros melanoxylon

2 references

Triterpene acids from Diospyros melanoxylon

Diospyros melanoxylon Leaves: A Rich Source of Pentacyclic Triterpenes

Eriobotrya japonica

5 references

Polyhydroxylated Triterpenes from Eriobotrya japonica

Anti-inflammatory constituents of topically applied crude drugs. I. Constituents and anti-inflammatory effect of Eriobotrya japonica LINDL

A New Triterpene Ester from Eriobotrya japonica.

Anti-inflammatory and antitumor-promoting effects of the triterpene acids from the leaves of Eriobotrya japonica

Anti-inflammatory constituents of topically applied crude drugs. I. Constituents and anti-inflammatory effect of Eriobotrya japonica LINDL

Eucalyptus albens

1 reference

Triterpene acids of some representatives ofEucalyptus

Eucalyptus camaldulensis

1 reference

Triterpene acids of some representatives ofEucalyptus

Eucalyptus globulus

1 reference

Triterpene acids of some representatives ofEucalyptus

Eucalyptus leucoxylon

1 reference

Triterpene acids of some representatives ofEucalyptus

Eucalyptus obliqua

1 reference

Triterpene acids of some representatives ofEucalyptus

Eucalyptus ovata

1 reference

Triterpene acids of some representatives ofEucalyptus

Eucalyptus perriniana

1 reference

Triterpenoids from Eucalyptus perriniana cultured cells

Eucalyptus polyanthemos

1 reference

Triterpene acids of some representatives ofEucalyptus

Eucalyptus sideroxylon

1 reference

Triterpene acids of some representatives ofEucalyptus

Eucalyptus viminalis

3 references

Maslinic acid from the leaves ofEucalyptus viminalis

Maslinic acid from the leaves ofEucalyptus viminalis

Maslinic acid from the leaves ofEucalyptus viminalis

Euptelea polyandra

4 references

Constituents of the Bark of Euptelea polyandra

Studies on inhibitors of skin-tumor promotion, I. Inhibitory effects of triterpenes from Euptelea polyandra on Epstein-Barr virus activation

Constituents of the Bark of Euptelea polyandra

Studies on inhibitors of skin-tumor promotion, I. Inhibitory effects of triterpenes from Euptelea polyandra on Epstein-Barr virus activation

Hyptis brevipes

2 references

Bioactive 5,6-dihydro-alpha-pyrone derivatives from Hyptis brevipes

Bioactive 5,6-dihydro-alpha-pyrone derivatives from Hyptis brevipes

Hyptis capitata

1 reference

The cytotoxic principles of Hyptis capitata and the structures of the new triterpenes hyptatic acid-A and -B

Hyptis mutabilis

1 reference

Chemistry of Hyptis mutabilis: new pentacyclic triterpenoids

Condea verticillata

1 reference

Cytotoxic constituents from Hyptis verticillata

Isodon flavidus

2 references

Diterpenoids from isodon flavidus

Diterpenoids from Isodon gesneroides

Lagerstroemia speciosa

1 reference

Screening of plant constituents for effect on glucose transport activity in Ehrlich ascites tumour cells

Lepechinia caulescens

2 references

Abietanoid acid from Lepechinia caulescens

Di- and triterpenoid acids from Lepechinia caulescens

Moquilea licaniaeflora

1 reference

Triterpenes from Licania licaniaeflora.

Ligusticum lucidum

1 reference

Chemical constituents from fruits of Ligustrum lucidum

Ligustrum obtusifolium

3 references

Studies on the Constituents of Ligustrum Species. VIII. On the Components of the Fruits of Ligustrum obtusifolium SIEB. et ZUCC. (2)

Studies on the Constituents of Ligustrum Species. XIII. : Structures of Phenylethanoid Glycosides from the Leaves of Ligustrum obtusifolium SIEB. et ZUCC.

Studies on the Constituents of Ligustrum Species. IX. On the Components of the Fruits of Ligustrum obtusifolium SIEB. et ZUCC. (3)

Luehea divaricata

1 reference

A New tormentic acid derivative from Luehea divaricata Mart. (Tiliaceae)

Luma chequen

1 reference

Flavonoids and terpenoids from Luma gayana (Barn.) Burret.

Lyonia ovalifolia

1 reference

Studies on the Constituents of the Leaves of Lyonia ovalifolia DRUDE in Nepal

Melaleuca leucadendra

1 reference

New Triterpenes from the Heartwood ofMelaleuca leucadendronL.

Salvia dianthera

1 reference

Sesquiterpenoid constituents of Meriandra benghalensis (Labiatae). X-ray structure analysis

Mucuna birdwoodiana

1 reference

Triterpenes from Mucuna birdwoodiana

Muntingia calabura

2 references

Activity-guided isolation of the chemical constituents of Muntingia calabura using a quinone reductase induction assay.

Activity-guided isolation of the chemical constituents of Muntingia calabura using a quinone reductase induction assay.

Musanga cecropioides

2 references

Cecropiacic acid, a new pentacyclic A-ring seco triterpenoid from Musanga cecropioides

Chemical Studies on the Cecropiaceae: A Novel A-ring Seco Triterpene from Musanga cecropioides

Myrianthus serratus

1 reference

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

Myrica rubra

4 references

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

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

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

Inhibitors of nitric oxide production from the bark of Myrica rubra: structures of new biphenyl type diarylheptanoid glycosides and taraxerane type triterpene

Ocimum spicatum

1 reference

Triterpenes and Sterols From Ocimum spicatum

Olea verrucosa

2 references

Components of the leaves ofOlea verrucosa

Components of the leaves ofOlea verrucosa

Orphium frutescens

1 reference

Xanthones and Triterpene Acids as Leaf Exudate Constituents in Orphium frutescens

Pourouma guianensis

1 reference

Antileishmanial activity of isolated triterpenoids from Pourouma guianensis.

Prunus africana

4 references

Characterization of Pygeum africanum bark extracts by HRGC with computer assistance

Triterpenes from Prunus africana bark

New constituents of Prunus africana bark extract

Triterpenes from Prunus africana bark

Punica granatum

3 references

Medicinal flowers. XXIII. New taraxastane-type triterpene, punicanolic acid, with tumor necrosis factor-alpha inhibitory activity from the flowers of Punica granatum

Constituents of the flowers of Punica granatum

Medicinal flowers. XXIII. New taraxastane-type triterpene, punicanolic acid, with tumor necrosis factor-alpha inhibitory activity from the flowers of Punica granatum

Scarlet firethorn

2 references

Two glucosides from Pyracantha coccinea roots: a new lignan and a new chalcone

Two glucosides from Pyracantha coccinea roots: a new lignan and a new chalcone

Isodon glutinosus

1 reference

Chemical Constituents of Paraboea glutinosa

Isodon yuennanensis

1 reference

Ent-kaurene diterpenoids from Rabdosia yuennanensis

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

Salvia canariensis

1 reference

Terpenoids of Cultivated Salvia canariensis

Salvia carduacea

1 reference

A new 24-nor-oleanane triterpenoid from Salvia carduacea

Salvia deserta

2 references

Triterpenoids from Salvia deserta

Triterpenoids from Salvia deserta

Salvia hierosolymitana

1 reference

Dammarane triterpenes of Salvia hierosolymitana

Salvia oxyodon

1 reference

Diterpenoids from Salvia oxyodon and Salvia lavandulifolia

Salvia palaestina

1 reference

Terpenoids from Salvia palaestina

Salvia verticillata

1 reference

Flavonoids and Terpenoids From Salvia verticillata and Salvia pinnata

Salvia virgata

2 references

Salvia willeana

2 references

Satureja montana

1 reference

Secondary Metabolites from Satureja Species. New Triterpenoid from Satureja acinos

Schnabelia tetradonta

1 reference

Chemical Constituents from the Roots of Schnabelia tetradonta.

Scutellaria strigillosa

1 reference

Studies on the constituents of Scutellaria species (XXI): constituents of the leaves of Scutellaria strigillosa Hemsley

Syringa reticulata

1 reference

Studies on the Constituents of Syringa Species. I. Isolation and Structures of Iridoids and Secoiridoids from the Leaves of Syringa reticulata (BLUME) HARA

clove

4 references

Triterpene acids of indian clove buds

An orsellinic acid glucoside from syzygium aromatica

Studies on Differentiation-Inducing Activities of Triterpenes

Effects of Syzygium aromaticum-derived triterpenes on postprandial blood glucose in streptozotocin-induced diabetic rats following carbohydrate challenge.

Terminalia chebula

1 reference

2α-Hydroxymicromeric acid, a pentacyclic triterpene from Terminalia chebula

Terminalia glabrescens

1 reference

Chemical constituents from Terminalia glabrescens

Terminalia pallida

1 reference

New constituents of Terminalia alata

Tetracentron sinense

1 reference

Two glycosides from the stem bark of Tetracentron sinense.

Thalictrum aquilegiifolium

1 reference

Isolation and structure of thalictoside.

Thomandersia laurifolia

3 references

Thomandersine and isothomandersine, 2-indolinone alkaloids from Thomandersia laurifolia

Thomandertriol, a Triterpenoid from the Twigs of Thomandersia laurifolia

Thomandersine and isothomandersine, 2-indolinone alkaloids from Thomandersia laurifolia

Complex-toothed flying squirrel

1 reference

Cytotoxic triterpenes from a Chinese medicine, Goreishi

Vitex altissima

2 references

Flavonoids, triterpenoids and a lignan from Vitex altissima

Flavonoids, triterpenoids and a lignan from Vitex altissima

Vochysia ferruginea

1 reference

6beta-hydroxymaslinic acid, a triterpene from Vochysia ferruginea

Ziziphus jujuba

1 reference

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

Rosa laevigata

2 references

Anti-inflammatory triterpenes from the leaves of Rosa laevigata

Anti-inflammatory triterpenes from the leaves of Rosa laevigata

Rubia yunnanensis

2 references

Biologically active arborinane-type triterpenoids and anthraquinones from Rubia yunnanensis

Biologically active arborinane-type triterpenoids and anthraquinones from Rubia yunnanensis

Symplocos lancifolia

2 references

Triterpenoid saponins from Symplocos lancifolia

Triterpenoid saponins from Symplocos lancifolia

Ligustrum japonicum

1 reference

Chemical constituents from fruits of Ligustrum lucidum

Actinidia chinensis

1 reference

Two new triterpenoids from the roots of Actinidia chinensis

Aegiceras corniculatum

1 reference

Unusual isomeric corniculatolides from mangrove, Aegiceras corniculatum

Buddleja asiatica

1 reference

Two New Oleanane-type Triterpenoids from Buddleja asiatica

Careya arborea

1 reference

Triterpenoid sapogenols from the leaves of Careya arborea: Structure of careyagenolide

Chaenomeles speciosa

1 reference

Antioxidant, anti-inflammatory and anti-influenza properties of components from Chaenomeles speciosa

Plectranthus rotundifolius

1 reference

Chemopreventive properties of phytosterols and maslinic acid extracted from Coleus tuberosus in inhibiting the expression of EBV early-antigen in Raji cells

Katmon

1 reference

Chemical studies on an endemic Philippine plant: sulfated glucoside and seco-A-ring triterpenoids from Dillenia philippinensis

Durio kutejensis

1 reference

Secondary Metabolites from the Wood Bark ofDuriozibethinusandDuriokutejensis

Euphorbia sororia

1 reference

Isoprenoids of Euphorbia sororia. I. Triterpenoids

Nothofagus pumilio

1 reference

Insect antifeedant compounds from Nothofagus dombeyi and N. pumilio.

Galphimia glauca

1 reference

Production of triterpenoids in liquid-cultivated hairy roots of Galphimia glauca

Gentiana dahurica

1 reference

Triterpenoids and Iridoid Glycosides from Gentiana dahurica

Juglans regia

1 reference

Antiproliferative triterpenes from the leaves and twigs of Juglans sinensis on HSC-T6 cells

Leucas aspera

1 reference

Diterpenes from Leucas aspera inhibiting prostaglandin-induced contractions

Microcos paniculata

1 reference

Chemical constituents with free-radical-scavenging activities from the stem of Microcos paniculata.

Photinia serratifolia

1 reference

Triterpenoids from the Edible Leaves ofPhotinia serrulata

Photinia serrulata

1 reference

Triterpenoids from the Edible Leaves ofPhotinia serrulata

Salvia miltiorrhiza

1 reference

Triterpenoids from the Flowers of Salvia miltiorrhiza

Salvia sahendica

1 reference

Sesterterpenoids and other constituents of Salvia sahendica.

Ulmus pumila

1 reference

New triterpenoids isolated from the root bark of Ulmus pumila L

Viburnum cylindricum

1 reference

Seven New Phenolic Glucosides fromViburnum cylindricum

Vitex agnus-castus

1 reference

A new diterpenoid glucoside and two new diterpenoids from the fruit of Vitex agnus-castus

Ziziphora clinopodioides

1 reference

Monoterpene glucosides from Ziziphora clinopodioides (Labiatae).

Mesosphaerum oblongifolium

1 reference

Structure and stereochemistry of four α-pyrones from Hyptis oblongifolia

Licania cariae

1 reference

Phytochemical investigations within the genus Duboisia

Moquilea cariae

1 reference

Phytochemical investigations within the genus Duboisia

Tripetaleia paniculata

1 reference

Studies on the Constituents of Tripetaleia paniculata SIEB. et ZUCC. V. On the Constituents of the Flowers and of the Wood.(3)

Olea europaea

6 references

Pentacyclic triterpene acids in olives

Cardiotonic and antidysrhythmic effects of oleanolic and ursolic acids, methyl maslinate and uvaol

Secreted oleanolic acid on the cuticleOlea europaea (Oleaceae); a chemical barrier to fungal attack

Oleanolic and maslinic acids of the fruit ofOlea europaea

Maslinic acid, a natural triterpene from Olea europaea L., induces apoptosis in HT29 human colon-cancer cells via the mitochondrial apoptotic pathway

Antioxidant activity of maslinic acid, a triterpene derivative obtained from Olea europaea

Syringa oblata

1 reference

Anti-inflammatory terpenoid derivatives from the twigs of Syringa oblata var. dilatata

Grewia bilamellata

1 reference

Antimalarial compounds from Grewia bilamellata.

Morella rubra

3 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

Inhibitors of nitric oxide production from the bark of Myrica rubra: structures of new biphenyl type diarylheptanoid glycosides and taraxerane type triterpene

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

Geum macrophyllum

4 references

Triterpenoids and glycosides from Geum japonicum

Anti-HIV triterpene acids from Geum japonicum

The anticoagulant effects ofGeum japonicum extract and its constituents

Terpenoids of Cultivated Salvia canariensis

Salvia fulgens

1 reference

Triterpene acids from Salvia and Teucrium species

Cantinoa mutabilis

1 reference

Chemistry of Hyptis mutabilis: new pentacyclic triterpenoids

Elliottia paniculata

1 reference

Studies on the Constituents of Tripetaleia paniculata SIEB. et ZUCC. V. On the Constituents of the Flowers and of the Wood.(3)

Salvia tomentosa

1 reference

A New Diterpene Acid From Salvia tomentosa

Salvia officinalis

1 reference

A New Diterpene Acid From Salvia tomentosa

Moquilea pyrifolia

1 reference

New Lupane Derivatives from the Leaves ofLicania pyrifolia

Syzygium sandwicense

1 reference

Constituents of Eugenia sandwicensis with potential cancer chemopreventive activity.

Photinia glabra

1 reference

Triterpenoids from the Edible Leaves ofPhotinia serrulata

Ligustrum lucidum

1 reference

Chemical constituents from fruits of Ligustrum lucidum

Salvia deserti

1 reference

Triterpenoids from Salvia deserta

Syzygium crebrinerve

1 reference

Extractives of Australian timbers. XVI. The constituents of the wood of Eugenia crebrinervis (syn. Syzigium crebrinerve) and Eugenia gustavioides (syn. Cleistocalyx gustavioides)

Syzygium gustavioides

1 reference

Extractives of Australian timbers. XVI. The constituents of the wood of Eugenia crebrinervis (syn. Syzigium crebrinerve) and Eugenia gustavioides (syn. Cleistocalyx gustavioides)

Duboisia myoporoides

1 reference

The separation of substituted Olean-12-en-28-oic acids from the corresponding Urs-12-en-28-oic acid isomers

subject has role

acid

0 references

Identifiers

InChI

InChI=1S/C30H48O4/c1-25(2)12-14-30(24(33)34)15-13-28(6)18(19(30)16-25)8-9-22-27(5)17-20(31)23(32)26(3,4)21(27)10-11-29(22,28)7/h8,19-23,31-32H,9-17H2,1-7H3,(H,33,34)/t19-,20+,21-,22+,23-,27-,28+,29+,30-/m0/s1

1 reference

Maslinic acid (English)

7 October 2016

InChIKey

2 references

Maslinic acid (English)

7 October 2016

ChEBI release 2020-09-01

2 references

maslinic acid (English)

7 October 2016

InChIKey

https://commonchemistry.cas.org/detail?cas_rn=4373-41-5

8 April 2021

1 reference

Maslinic acid (English)

7 October 2016

1 reference

Maslinic acid (English)

7 October 2016

Reaxys registry number

2711878

1 reference

maslinic acid (English)

7 October 2016

ChEBI ID

66682

mapping relation type

1 reference

maslinic acid (English)

7 October 2016

1 reference

MASLINIC ACID (English)

7 October 2016

1 reference

1 reference

MassBank accession ID

MSBNK-RIKEN-PR303806

1 reference

InChIKey

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

Hazardous Substances Data Bank

28 October 2019

Maslinic Acid (English)

DSSTOX compound identifier

10 May 2021

DSSTox substance ID

DTXSID30905074

0 references

DTXCID101334176

0 references

EC number

610-137-3

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.128.873

27 December 2018

ECHA Substance Infocard ID

Olean-12-en-28-oic acid, 2,3-dihydroxy-, (2α,3β)- (English)

quotation

CAS no.: 4373-41-5 (English)

100.128.873

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.128.873

27 December 2018

Human Metabolome Database ID

Olean-12-en-28-oic acid, 2,3-dihydroxy-, (2α,3β)- (English)

quotation

CAS no.: 4373-41-5 (English)

HMDB0002392

1 reference

UNII

E233J88OHQ

1 reference

Global Substance Registration System

UNII

E233J88OHQ

MASLINIC ACID (English)

7 October 2016

0 references

1 reference

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

maslinic acid (English)

7 October 2016

1 reference