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Embelin

HCID 3218
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
550-24-3
Standard SMILES
CCCCCCCCCCCC1=C(O)C(=O)C=C(O)C1=O
InChIKey
IRSFLDGTOHBADP-UHFFFAOYSA-N
Molecular formula
C17H26O4
Average molar mass
294.4 g/mol
Monoisotopic mass
294.18310931

Overview

Embelin is a member of the class of dihydroxy-1,4-benzoquinones that is 2,5-dihydroxy-1,4-benzoquinone which is substituted by an undecyl group at position 3. Isolated from Lysimachia punctata and Embelia ribes, it exhibits antimicrobial, antineoplastic and inhibitory activity towards hepatitis C protease. It has a role as an antimicrobial agent, an antineoplastic agent, a hepatitis C protease inhibitor and a plant metabolite.

Names & identifiers

Preferred name
Embelin
IUPAC
2,5-dihydroxy-3-undecylcyclohexa-2,5-diene-1,4-dione
English name
EMBELIN
Molecular formula
C17H26O4
Molecular weight
294.39

Names & synonyms

EMBELIN550-24-3Embelic acidEmberine2,5-Dihydroxy-3-undecyl-1,4-benzoquinone2,5-Dihydroxy-3-undecyl-p-benzoquinone2,5-Dihydroxy-3-undecyl-2,5-cyclohexadiene-1,4-dioneSHC6U8F5ERCHEBI:4778p-Benzoquinone, 2,5-dihydroxy-3-undecyl-DTXSID80203537NSC-91874
Show more names
NSC 91874Embelin-RMembelicacidEmbelin, >98%XIAP INHIBITOREMbeliaquinoneEmbelin (Standard)TIMTEC-BB SBB005949
RefChem:136587DTXCID10126028208-979-82,5-dihydroxy-3-undecylcyclohexa-2,5-diene-1,4-dioneMFCD00016369NSC918742,5-Cyclohexadiene-1,4-dione, 2,5-dihydroxy-3-undecyl-2,5-Dihydroxy-3-undecyl-[1,4]benzoquinone

Database identifiers

CAS
550-24-3
PubChem CID
3218
DTXSID
DTXSID80203537
ChEMBL
CHEMBL221137

Properties

Computed structural properties

XLogP
5.4
Topological polar surface area
74.6 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
4
Rotatable bonds
10
Heavy atoms
21
Formal charge
0
Complexity
432

Experimental & physicochemical properties

LipidsLipids -> Polyketides [PK] -> Phenolic lipids [PK15] -> Alkyl hydroquinones and derivatives [PK1505]

Physicochemical properties

Melting point
142 · 142-143°C
Boiling point
356.15 °C · 356.15°C (rough estimate)
Density
1.131 · 1.131
refractive index
1.423 · 1.4230 (estimate)
storage temp.
2 · Keep in dark place,Inert atmosphere,2-8°C
solubility
10 mg/mL · DMSO: >10 mg/mL
form
solid
pka
2.84 · 2.84±0.50(Predicted)
color
Dark orange
Sensitive
Light Sensitive
Stability
1 year · Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
InChI
1S/C17H26O4/c1-2-3-4-5-6-7-8-9-10-11-13-16(20)14(18)12-15(19)17(13)21/h12,18,21H,2-11H2,1H3

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 4 items

Warning

H361 (75%): Suspected of damaging fertility or the unborn child [Warning Reproductive toxicity]

P203, P273, P280, P318, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 4 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Hazard Classes and CategoriesRepr. 2 (75%)

Safety data

PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
rtecs
DK4230000
Signal word
Warning
Symbol(GHS)
GHS08
Storage Class
11 - Combustible Solids
Hazard statements
H361f
Hazard Classifications
Repr. 2
Precautionary statements
P201-P308+P313

Chemistry & industry

Applications · 2 items

DescriptionEmbelin (550-24-3) inhibitsthe lysine acetyl transferase PCAFin vitro and in vivo(in vitroIC50=7.2 mM). Inhibits H3K9 acetylation in mouse liver tissue while leaving levels of H3K14, H4K8, H4K12 unchanged.1 Also inhibits X-linked inhibitor of apoptosis (XIAP) (IC50 = 4.1 μM, competing with Smac peptide). Binds to the BIR3 domain, preventing XIAP interaction with caspase-9 and Smac. Induces apoptosis and alters gene expression profiles in breast cancer cells.3Possesses anti-inflammatory and analgesic activityin vivo.4Cell-permeable.

UsesEmbelin is a natural benzoquinone found in plants of the Myrsinaceae family. Embelin has a wide range of biological activity as it inhibits the growth of bacteria, fungi, protozoa and parasites. Embelin also displays contraceptive and pro-apoptotic properties.

Upstream & downstream products

Downstream products

Acetic acid 4-acetoxy-3,6-dioxo-5-undecyl-cyclohexa-1,4-dienyl ester

Suppliers100 total

成都普瑞法科技开发有限公司+86-028-82633397 18982077548 · [email protected]
南通飞宇生物科技有限公司0513-68819626 15152877458 · [email protected]
成都埃法生物科技有限公司028-028-85142057 19983342022 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
成都彼样生物科技有限公司18108052721 · [email protected]
合肥翰刚医药科技有限公司

Related reactions

1 records
New reaction record
HRID 899553 reaction equation
HRID 899553As reactantuspto-grants-2008_04

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
ChEBI
CHEBI:4778
UNII
SHC6U8F5ER
EC Number
208-979-8
Nikkaji
J6.710E
InChIKey
IRSFLDGTOHBADP-UHFFFAOYSA-N
SMILES
CCCCCCCCCCCC1=C(O)C(=O)C=C(O)C1=O
LogP
5.024 · 5.024 (est)
FDA UNII
6 U8F5ER · SHC6U8F5ER
UNSPSC Code
41116107 · 41116107
NACRES
77 · NA.77
Symbol(GHS)
8 · GHS08
Signal word
Warning
Hazard statements
361 f · H361f
Precautionary statements
201 · P201-P308+P313
PPE
95 · Eyeshields, Gloves, type N95 (US)
WGK Germany
3 · 3
RTECS
4230000 · DK4230000
Storage Class
11 · 11 - Combustible Solids
Hazard Classifications
2 · Repr. 2
+8618062405514 · [email protected]
成都健腾生物技术有限公司028-85159085 18080455027 · [email protected]
成都市久鼎化学技术有限公司18584079237 · [email protected]
云南西力生物技术股份有限公司0871-65217109 · [email protected]
Syntechem Co.,Ltd[email protected]
武汉易泰科技有限公司上海分公司18930552037 · [email protected]
上海晶抗生物工程有限公司021-54721350 13524668266 · [email protected]
上海颖心实验室设备有限公司021-59178156 17002132182 · [email protected]
大连美仑生物技术有限公司0411-62910999 13889544652 · [email protected]
Hangzhou Sage Chemical Co., Ltd.+86057186818502 13588463833 · [email protected]
安耐吉化学&3A(安徽泽升科技有限公司)021-58432009 400-005-6266 · [email protected]
武汉凯威斯科技有限公司86-027-67849912 · [email protected]
上海诗丹德标准技术服务有限公司021-021-57127007-6622-6622 17621252073 · [email protected]
成都普思生物科技股份有限公司028-85370565-229 18080489829 · [email protected]
InvivoChem中国13549236410 · [email protected]
MedBio脉铂医药021-69568360 18916172912 · [email protected]
MedChemexpress LLC021-58955995 · [email protected]
医恩医疗系统研发(上海)有限公司021-58958002 18930822973 · [email protected]
武汉丰泰威远科技有限公司+86-27-8746-5837 +86-18627785180 · [email protected]
武汉丰泰威远科技有限公司027-87465837 19945049750 · [email protected]
佛山宝诺生物科技有限公司0757-85921206 18520245316 · [email protected]
Aktin Chemicals, Inc.028-85159085 · [email protected]
ChemeGen 中国18818260767 · [email protected]
南京斯贝源医药科技有限公司+86-25-68710855, +86-25-68710897 · [email protected]
斯百全化学(上海)有限公司021-021-021-67601398-809-809-809 15221380277 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
江苏艾康生物医药研发有限公司025-66113011 13913916777 · [email protected]
广州爱纯医药科技有限公司020-39119399 18927568969 · [email protected]
雷丁试剂0510-85629785 18013409632 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
杭州杰恒化工有限公司0571-87396432 · [email protected]
上海永叶生物科技有限公司86-021-61559134 15921386130 · [email protected]
南京百鑫德诺生物科技有限公司025-58849295 · [email protected]
凯试(上海)科技有限公司021-50135380 · [email protected]
湖北巨胜科技有限公司027-59599241 18871490274 · [email protected]
ALB Technology Limited702-983-3769 · [email protected]
成都钠钶锂生物科技有限公司028-61983833 19138982515 · [email protected]
TargetMol中国(陶术生物)021-021-33632979 15002134094 · [email protected]
武汉天植生物技术有限公司18607101326 15172504745 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
上海萄普生物医药技术有限公司15900573766 18018507602 · [email protected]
BOC Sciences16314854226; +8616314854226 · [email protected]
Wuhan ChemNorm Biotech Co.,Ltd.+86-27-8439 4403 18971486879 · [email protected]
陕西缔都医药化工有限公司029-029-81120477 17792793610 · [email protected]
上海珞珐生化科技有限公司021-51111890 15317326293 · [email protected]
Additional notes · 1 item

DefinitionChEBI: A member of the class of dihydroxy-1,4-benzoquinones that is 2,5-dihydroxy-1,4-benzoquinone which is substituted by an undecyl group at position 3. Isolated from Lysimachia punctata and Embelia ribes, it exhibits antimicrobial, an ineoplastic and inhibitory activity towards hepatitis C protease.