CD1530

CD1530 Suppliers list
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com
Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
Tel: 021-52996696,15000506266 15000506266
Email:
Company Name: EMMX Biotechnology LLC  
Tel: 888-539-0666
Email: info@emmx.com
Company Name: ShangHai Biochempartner Co.,Ltd  
Tel: 177-54423994 17754423994
Email: 2853530910@QQ.com
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 13301690235
Email: Sales@ATKchemical.com

CD1530 manufacturers

  • CD 1530
  • CD 1530 pictures
  • 2026-07-08
  • CAS:107430-66-0
  • Purity: 98.13%
  • Supply Ability: 10g
CD1530 Basic information
Product Name:CD1530
Synonyms:4-(6-Hydroxy-7-tricyclo[3.3.1.13,7]dec-1-yl-2-naphthalenyl)benzoicacid;Benzoic acid, 4-(6-hydroxy-7-tricyclo[3.3.1.13,7]dec-1-yl-2-naphthalenyl)-;CD1530;CD1530 >=98% (HPLC);4-(7-(Adamantan-1-yl)-6-hydroxynaphthalen-2-yl)benzoic acid
CAS:107430-66-0
MF:C27H26O3
MW:398.49
EINECS:
Product Categories:
Mol File:107430-66-0.mol
CD1530 Structure
CD1530 Chemical Properties
Boiling point 610.7±55.0 °C(Predicted)
density 1.290±0.06 g/cm3(Predicted)
storage temp. Store at +4°C
solubility 50 mM in 1 eq. NaOH: Soluble
form powder
pka4.13±0.10(Predicted)
color white to beige
InChI1S/C27H26O3/c28-25-12-22-6-5-21(19-1-3-20(4-2-19)26(29)30)10-23(22)11-24(25)27-13-16-7-17(14-27)9-18(8-16)15-27/h1-6,10-12,16-18,28H,7-9,13-15H2,(H,29,30)
InChIKeyVCQGNUWOMLYNNG-UHFFFAOYSA-N
SMILESOC1=CC2=C(C=C(C3=CC=C(C(O)=O)C=C3)C=C2)C=C1C4(C[C@H](C5)C6)C[C@H]6C[C@H]5C4
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
CD1530 Usage And Synthesis
UsesCD 1530 is a retinoic acid receptor γ selective agonist. In combination with bexxarotene, they inhibit murine oral-cavity carcinogensis. It is found to inhibit heterotopic ossification and preserve tendon stem cell characteristics. It is also associated with RAR signalling in asthma.
Biological ActivityPotent and selective RAR γ receptor agonist (K i values are 150, 1500 and 2750 nM for RAR γ , RAR β and RAR α receptors respectively). Activates transcriptional activity (AC 50 = 1.8 nM).
in vivo

CD1530 (4 mg/kg; p.o.; once every other day) inhibits FOP-like heterotopic ossification in transgenic mice carrying a Cre-inducible constitutively active ALK2Q207D mutation[1].
CD1530 (2.5 mg/100 mL; p.o., in drinking water; frequency not mentioned; 15 weeks) combined with 4-nitroquinoline 1-oxide reduces the number and severity of tongue tumor lesions in mice with oral cancer[3].
CD1530 (10 μg; local injection; 3 times per week; 3 weeks) accelerates tendon healing in mice with Achilles tendon rupture, inhibits cartilage formation, reduces fibrous tissue-like scar formation, and promotes better collagen fiber alignment[4].
CD1530 (4 mg/kg, p.o.; or 1 mM, intramuscular injection; once a day; administration for 4 weeks) can inhibit muscle fat infiltration, reduce the number of intramuscular adipocytes, and reduce the expression of adipogenic marker genes in mice with rotator cuff tear[6].

Animal Model:C57BL/6 male mice (weight approximately 23 g, 9 weeks old) + rotator cuff tear model[6]
Dosage:4 mg/kg (orally administered); 1 mM (intramuscular injection, solvent: dimethyl sulfoxide)
Administration:Oral administration, once a day, for 4 weeks; Intramuscular injection, once a week, for 4 weeks
Result:Significantly suppressed fatty infiltration in the supraspinatus muscle (p.o.).
Reduced the ratio of the fat area to the muscle cross-sectional area and the expression of adipogenic marker genes Pparg and Cebpa (p.o.).
Reduced fatty infiltration in the supraspinatus muscle (intramuscular injection).
storageStore at +4°C
CD1530 Preparation Products And Raw materials
Tag:CD1530(107430-66-0) Related Product Information
4-(Naphthalen-2-yl)benzoic acid CD1530 Hydroxy Adapalene 3,5-Di-tert-butyl-4-hydroxybenzoic acid 5-(Cyclohexylmethyl)-2-hydroxybenzoic acid (1,1'-Biphenyl)-3-carboxylic acid, 4'-(1,1-dimethylethyl)-4-hydroxy-