(Q27134961)

English

moromycin B

chemical compound

In more languages

Statements

type of chemical entity

0 references

benzo[a]anthracene polyketide

0 references

562.183897±0 dalton

1 reference

language of work or name

Moromycin B (English)

7 October 2016

chemical formula

C₃₁H₃₀O₁₀

1 reference

language of work or name

Moromycin B (English)

7 October 2016

canonical SMILES

CC1C2C(CC(O1)C3=C(C4=C(C=C3)C(=O)C5=C(C4=O)C=CC6=C5C(=O)CC(C6)(C)O)O)OC7CC(=O)C(OC7O2)C

1 reference

language of work or name

Moromycin B (English)

7 October 2016

isomeric SMILES

C[C@@H]1[C@@H]2[C@@H](C[C@@H](O1)C3=C(C4=C(C=C3)C(=O)C5=C(C4=O)C=CC6=C5C(=O)C[C@](C6)(C)O)O)O[C@H]7CC(=O)[C@@H](O[C@H]7O2)C

1 reference

language of work or name

Moromycin B (English)

7 October 2016

7 references

Moromycins A and B, isolation and structure elucidation of C-glycosylangucycline-type antibiotics from Streptomyces sp. KY002.

Moromycins A and B, isolation and structure elucidation of C-glycosylangucycline-type antibiotics from Streptomyces sp. KY002.

Moromycins A and B, isolation and structure elucidation of C-glycosylangucycline-type antibiotics from Streptomyces sp. KY002.

Moromycins A and B, isolation and structure elucidation of C-glycosylangucycline-type antibiotics from Streptomyces sp. KY002.

Saquayamycins G-K, cytotoxic angucyclines from Streptomyces sp. Including two analogues bearing the aminosugar rednose

Cytotoxic antibiotic angucyclines and actinomycins from the Streptomyces sp. XZHG99T

Cytotoxic, Anti-Migration, and Anti-Invasion Activities on Breast Cancer Cells of Angucycline Glycosides Isolated from a Marine-Derived Streptomyces sp.

Identifiers

InChI=1S/C31H30O10/c1-12-18(32)8-22-30(39-12)41-29-13(2)38-20(9-21(29)40-22)15-6-7-17-25(26(15)34)28(36)16-5-4-14-10-31(3,37)11-19(33)23(14)24(16)27(17)35/h4-7,12-13,20-22,29-30,34,37H,8-11H2,1-3H3/t12-,13+,20+,21+,22-,29+,30-,31+/m0/s1

1 reference

language of work or name

Moromycin B (English)

7 October 2016

IVVLBSCKLIYBCU-GEMPFEMJSA-N

2 references

language of work or name

Moromycin B (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

moromycin B (English)

7 October 2016

IVVLBSCKLIYBCU-GEMPFEMJSA-N

CAS Common Chemistry

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=1044869-33-1

1 reference

language of work or name

(3R)-9-[(2S,4aS,5aR,7R,9R,9aR,10aR)-2,9-Dimethyl-3-oxooctahydro-2H,5aH-dipyrano[2,3-b:4',3'-e][1,4]dioxin-7-yl]-3,8-dihydroxy-3-methyl-3,4-dihydro-1,7,12(2H)-tetraphenetrione (English)

7 October 2016

2 references

language of work or name

Moromycin B (English)

7 October 2016

matched by identifier from

IVVLBSCKLIYBCU-GEMPFEMJSA-N

Reaxys registry number

19172513

1 reference

language of work or name

moromycin B (English)

7 October 2016

mapping relation type

2 references

language of work or name

moromycin B (English)

7 October 2016

matched by identifier from

International Chemical Identifier

InChI=1S/C31H30O10/c1-12-18(32)8-22-30(39-12)41-29-13(2)38-20(9-21(29)40-22)15-6-7-17-25(26(15)34)28(36)16-5-4-14-10-31(3,37)11-19(33)23(14)24(16)27(17)35/h4-7,12-13,20-22,29-30,34,37H,8-11H2,1-3H3/t12-,13+,20+,21+,22-,29+,30-,31+/m0/s1

1 reference

language of work or name

MOROMYCIN B (English)

7 October 2016

UniChem compound ID

1 reference

DSSTox substance ID

DTXSID601098684

1 reference

matched by identifier from

IVVLBSCKLIYBCU-GEMPFEMJSA-N

Natural Product Atlas ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

IVVLBSCKLIYBCU-GEMPFEMJSA-N

Sitelinks

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