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Nodosin - 99%, high purity , CAS No.10391-09-0

COA

Grade & Purity:

≥99%

Cas Number: 10391-09-0
Molecular Weight: 362.42
PubChem CID: 10248089

In stock

Item Number

N649311

Grouped product items
SKU	Size	Availability	Price
N649311-1mg	1mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$110.90
N649311-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$229.90
N649311-10mg	10mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$339.90

Terpenoids Diterpenoids

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Diterpenoid (1) Terpenoids Diterpenoids (31)

Basic Description

Synonyms	AKOS032962396 \| HY-N3181 \| 11-Deacetylsinuolatin E; NSC 285659; Nodosin (terpene) \| NODOSIN \| CHEBI:70379 \| F92771 \| CS-0023521 \| Q27138718 \| (1S,4S,8R,9R,12S,13S,14R,16S)-9,14-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.
Specifications & Purity	≥99%
Biochemical and Physiological Mechanisms	Nodosin is a diterpenoid isolated from Isodon trichocarpus Kudo and I. Japonicus HARA.
Storage Temp	Protected from light,Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Nodosin is a diterpenoid isolated from Isodon trichocarpus Kudo and I. Japonicus HARA. Form:Solid

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Prenol lipids
    - Subclass Terpene lactones

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Prenol lipids
Subclass	Terpene lactones
Intermediate Tree Nodes	Not available
Direct Parent	Diterpene lactones
Alternative Parents	Kaurane diterpenoids Delta valerolactones Oxanes Tetrahydrofurans Secondary alcohols Ketones Hemiacetals Cyclic alcohols and derivatives Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic heteropolycyclic compounds
Substituents	Diterpene lactone - Diterpenoid - Kaurane diterpenoid - Delta valerolactone - Delta_valerolactone - Oxane - Cyclic alcohol - Tetrahydrofuran - Carboxylic acid ester - Hemiacetal - Ketone - Lactone - Secondary alcohol - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Carbonyl group - Organic oxide - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.
External Descriptors	delta-lactone
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

HL-60 (67320 Activities)

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K562 (73714 Activities)

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MCF7 (126967 Activities)

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SW480 (6023 Activities)

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T-24 (2342 Activities)

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UMUC3 (278 Activities)

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A549 (127892 Activities)

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HepG2 (196354 Activities)

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SMMC-7721 (5516 Activities)

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Associated Targets(non-human)

RAW264.7 (28094 Activities)

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Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	(1S,4S,8R,9R,12S,13S,14R,16S)-9,14-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione
INCHI	InChI=1S/C20H26O6/c1-9-10-6-11(21)13-19(7-10,15(9)22)17(24)26-12-4-5-18(2,3)14-16(23)25-8-20(12,13)14/h10-14,16,21,23H,1,4-8H2,2-3H3/t10-,11-,12+,13-,14-,16-,19+,20+/m1/s1
InChIKey	WZYJEEIAFBHYJS-SONIPUFESA-N
Smiles	CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C
Isomeric SMILES	CC1(CC[C@H]2[C@]3([C@@H]1[C@@H](OC3)O)[C@@H]4[C@@H](C[C@@H]5C[C@]4(C(=O)C5=C)C(=O)O2)O)C
Alternate CAS	10391-09-0
PubChem CID	10248089
MeSH Entry Terms	nodosin
Molecular Weight	362.42

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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9 results found

Lot Number	Certificate Type	Date	Item
C2507509	Certificate of Analysis	Oct 22, 2024	N649311
C2507506	Certificate of Analysis	Oct 22, 2024	N649311
C2513477	Certificate of Analysis	Oct 22, 2024	N649311
C2513478	Certificate of Analysis	Oct 22, 2024	N649311
C2513480	Certificate of Analysis	Oct 22, 2024	N649311
C2507507	Certificate of Analysis	Oct 22, 2024	N649311
C2507508	Certificate of Analysis	Oct 22, 2024	N649311
C2507574	Certificate of Analysis	Oct 22, 2024	N649311
C2507575	Certificate of Analysis	Oct 22, 2024	N649311

Chemical and Physical Properties

Solubility	125 mg/mL (344.90 mM; ultrasound assisted dissolution,<60 ℃)
Sensitivity	light sensitive
Flash Point(°F)	431.78℉
Flash Point(°C)	222.1℃
Boil Point(°C)	615.3℃ at 760mmHg
Molecular Weight	362.400 g/mol
XLogP3	1.500
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	0
Exact Mass	362.173 Da
Monoisotopic Mass	362.173 Da
Topological Polar Surface Area	93.100 Å²
Heavy Atom Count	26
Formal Charge	0
Complexity	728.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	8
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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Nodosin - 99%, high purity , CAS No.10391-09-0

Basic Description

Taxonomic Classification

Associated Targets(Human)

Associated Targets(non-human)

Mechanisms of Action

Names and Identifiers

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

Chemical and Physical Properties

Solution Calculators

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

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