(Q105370929)

English

4-[(3R,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]benzene-1,2-diol

chemical compound

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instance of

type of chemical entity

0 references

subclass of

4-(3,7,11-Trimethyldodeca-1,6,10-trien-3-yl)benzene-1,2-diol

1 reference

1 reference

314.2245802 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₂₁H₃₀O₂

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canonical SMILES

OC1=CC=C(C=C1O)C(C=C)(C)CCC=C(C)CCC=C(C)C

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isomeric SMILES

C=C[C@@](C)(CC/C=C(\C)CCC=C(C)C)c1ccc(O)c(O)c1

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found in taxon

Piper peltatum

4 references

stated in

Inhibitory effects of Piper umbellatum and Piper peltatum extracts towards myotoxic phospholipases A2 from Bothrops snake venoms: isolation of 4-nerolidylcatechol as active principle

stated in

HIV inhibitory natural products. 6. The peltatols, novel HIV-inhibitory catechol derivatives from Pothomorphe peltata

stated in

Cytotoxic 4-nerolidylcatechol from Pothomorphe peltata inhibits topoisomerase I activity

stated in

4-Nerolidylcatechol from Pothomorphe spp. scavenges peroxyl radicals and inhibits Fe(II)-dependent DNA damage

Piper umbellatum

4 references

stated in

Inhibitory effects of Piper umbellatum and Piper peltatum extracts towards myotoxic phospholipases A2 from Bothrops snake venoms: isolation of 4-nerolidylcatechol as active principle

stated in

Bioactive aristolactams from Piper umbellatum

stated in

In vitro and in vivo inhibition of skin matrix metalloproteinases by Pothomorphe umbellata root extract

stated in

4-Nerolidylcatechol from Pothomorphe spp. scavenges peroxyl radicals and inhibits Fe(II)-dependent DNA damage

Identifiers

InChI

InChI=1S/C21H30O2/c1-6-21(5,18-12-13-19(22)20(23)15-18)14-8-11-17(4)10-7-9-16(2)3/h6,9,11-13,15,22-23H,1,7-8,10,14H2,2-5H3/b17-11+/t21-/m0/s1

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InChIKey

ZBZZDHDWRSFLAY-RKPWUKJMSA-N

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1 reference

17 September 2022

inferred from InChIKey

(Q105370929)

4-[(3R,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]benzene-1,2-diol

Statements

Identifiers

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