(7R,13R,17R)-17-[2-[4-(diethylaminomethyl)-2-methoxyphenoxy]ethyl]-7,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol;2-hydroxypropane-1,2,3-tricarboxylic acid , Estrogen receptor alpha antagonist, CAS No.16047027, Estrogen receptor alpha antagonist

CAS: 16047027 Cat. No.: H671126 Molecular Weight: 697.9 PubChem CID: 16047027
AVAILABLE TO ORDER
Synonyms
HLX-801 | TS-108 | CHEMBL3545210 | SR-16234
Storage
Room temperature
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Size
Status
Price
Qty
1mg
H671126-1mg
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$999.90
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Why this grade

for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
HLX-801 | TS-108 | CHEMBL3545210 | SR-16234
Storage
Room temperature
Action Type
ANTAGONIST
Mechanism of action
Estrogen receptor alpha antagonist
Names and Identifiers
Canonical SmilesCCN(CC)CC1=CC(=C(C=C1)OCCC2CCC3C2(CCC4C3C(CC5=C4C=CC(=C5)O)C)C)OC.C(C(=O)O)C(CC(=O)O)(C(=O)O)O
IUPAC Name(7R,13R,17R)-17-[2-[4-(diethylaminomethyl)-2-methoxyphenoxy]ethyl]-7,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol;2-hydroxypropane-1,2,3-tricarboxylic acid
InChIKeyVOHOCSJONOJOSD-RQIKCBEZSA-N
INCHI1S/C33H47NO3.C6H8O7/c1-6-34(7-2)21-23-8-13-30(31(19-23)36-5)37-17-15-25-9-12-29-32-22(3)18-24-20-26(35)10-11-27(24)28(32)14-16-33(25,29)4;7-3(8)1-6(13,5(11)12)2-4(9)10/h8,10-11,13,19-20,22,25,28-29,32,35H,6-7,9,12,14-18,21H2,1-5H3;13H,1-2H2,(H,7,8)(
Isomeric SMILES CCN(CC)CC1=CC(=C(C=C1)OCC[C@H]2CCC3[C@@]2(CCC4C3[C@@H](CC5=C4C=CC(=C5)O)C)C)OC.C(C(=O)O)C(CC(=O)O)(C(=O)O)O
PubChem CID 16047027
Molecular Weight 697.9

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassSteroids and steroid derivatives
SubclassPregnane steroids
Intermediate Tree Nodes Not available
Direct ParentGluco/mineralocorticoids, progestogins and derivatives
Alternative Parents 3-hydroxysteroids  Phenanthrenes and derivatives  Tetralins  Tricarboxylic acids and derivatives  Anisoles  Benzylamines  Methoxybenzenes  Phenoxy compounds  Phenylmethylamines  Aralkylamines  Alkyl aryl ethers  1-hydroxy-2-unsubstituted benzenoids  Alpha hydroxy acids and derivatives  Tertiary alcohols  Trialkylamines  Carboxylic acids  Hydrocarbon derivatives  Carbonyl compounds  Organic oxides  
Molecular FrameworkNot available
Substituents Progestogin-skeleton - 3-hydroxysteroid - Hydroxysteroid - Phenanthrene - Tetralin - Tricarboxylic acid or derivatives - Phenoxy compound - Anisole - Benzylamine - Methoxybenzene - Phenol ether - Phenylmethylamine - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Aralkylamine - Phenol - Alpha-hydroxy acid - Monocyclic benzene moiety - Benzenoid - Hydroxy acid - Tertiary alcohol - Tertiary aliphatic amine - Tertiary amine - Ether - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Alcohol - Organic oxide - Amine - Organonitrogen compound - Organooxygen compound - Aromatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as gluco/mineralocorticoids, progestogins and derivatives. These are steroids with a structure based on a hydroxylated prostane moiety.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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