(Q82877514)

English

Mallotolerin

chemical compound

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Statements

type of chemical entity

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chemical compound

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488.204632604 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₂₆H₃₂O₉

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canonical SMILES

O=C(C=1C(O)=C(C(OC)=C(C1O)CC2=C(O)C(=C(O)C(=C2O)CC(O)C(=C)C)C(=O)CCC)C)C

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Mallotus japonicus

6 references

Inhibition of HIV-reverse transcriptase activity by some phloroglucinol derivatives

Studies on cytotoxic constituents in pericarps of Mallotus japonicus. IV.

Prostaglandin E(2) production and induction of prostaglandin endoperoxide synthase-2 is inhibited in a murine macrophage-like cell line, RAW 264.7, by Mallotus japonicus phloroglucinol derivatives

Constituents of the Pericarps of Mallotus japonicus (Euphorbiaceae)

Inhibition of tumor-promoter-enhanced 3H-choline incorporation into cellular phospholipids by phloroglucinol derivatives from Mallotus japonicus

Studies on cytotoxic constituents in pericarps of Mallotus japonicus, Part II.

Lotus japonicus

1 reference

Cytotoxic and antiherpetic activity of phloroglucinol derivatives from Mallotus japonicus (Euphorbiaceae)

Identifiers

InChI=1S/C26H32O9/c1-7-8-17(28)20-23(32)14(22(31)15(24(20)33)10-18(29)11(2)3)9-16-25(34)19(13(5)27)21(30)12(4)26(16)35-6/h18,29-34H,2,7-10H2,1,3-6H3

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AELVJBIXVGTXMM-UHFFFAOYSA-N

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CAS Registry Number

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2 references

26 December 2021

matched by identifier from

AELVJBIXVGTXMM-UHFFFAOYSA-N

UniChem compound ID

1 reference

DSSTox substance ID

1 reference

matched by identifier from

AELVJBIXVGTXMM-UHFFFAOYSA-N

DSSTOX compound identifier

DTXCID501337203

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